Abstract
Presently, functional foods and nutraceuticals are gaining immense importance in the prevention of various maladies through dietary regimen module. Consumption of fruits and vegetables based diet has pursuit a range of bioactive components, especially phytochemicals targeting life threatening ailments. In this context, lycopene is an extensively studied antioxidant potentially present in watermelon, tomato, pink guava etc. Watermelon is one of the unique sources having readily available cis-isomeric lycopene. The distinctive aroma of watermelon is imparted by medium- and short-chain fatty acids along with geranial, ß-ionone and neral. Its consumption has been escalated owing to rich nutritional profile and allied health benefits. It is effective in reducing the extent of cancer insurgence, cardiovascular disorders, diabetes and macular diseases. The structural characteristics, physiochemical properties and therapeutic effects of lycopene are the limelight of the manuscript. However, further research investigations are still needed to address the health enhancing potential of watermelon lycopene.
Keywords: functional foods, watermelon, lycopene, cancer, cardiovascular disorders, macular diseases
Background
Accumulating evidences have established a consensus that fruits are concentrated source of natural components thus having health promoting properties (Butt et al., 2008[19]). Plant based diet contains several bioactive ingredients with vital role to perform various metabolic functions like growth, development and protective mechanism against physiological threats. In this context, phytochemicals are of significance importance as they improve the human health through distinct pathways. The plants that are rich sources of bioactive molecules include garlic, ginger, tea, ginseng, black cumin, mulberry, raspberry etc. (Butt et al., 2009[20]). Researchers are focusing on exploitation of natural resources for dietary regimen against life threatening ailments (Lucier and Lin, 2001[74]).
Watermelon (Citrullus lanatus), botanically considered as a fruit, belongs to the family Cucurbitaceae (Edwards et al., 2003[37]). It is native to Kalahari desert of Africa but nowadays, it is also cultivated in tropical regions of the world. In the pages of history, its first harvest was documented 5000 years ago in Egypt that later spread to other part of the world. Presently, China is the top producer followed by Turkey, United States, Iran and Republics of Korea (Zohary and Hopf, 2000[119]; Lucier and Lin, 2001[74]; Naz et al., 2013[89]). Watermelon is a valued source of natural antioxidants with special reference to lycopene, ascorbic acid and citruline. These functional ingredients act as protection against chronic health problems like cancer insurgence and cardiovascular disorders (Zhang and Hamauzu, 2004[118]; Omoni and Aluko, 2005[91]; Fenko et al., 2009[40]). Lycopene is characterized by its distinctive red color in fruits and vegetable (Mutanen and Pajari, 2011[87]).
During the last few decades, presence of appreciable quantity of lycopene in watermelon has motivated the farmers/growers to cultivate high red flesh varieties. Overall, twelve hundred cultivars of watermelon are produced worldwide while the four most promising cultivars are picnic, icebox, yellow flesh and seed less (Chalabi et al., 2006[23]; Helyes et al., 2009[48]). This review article intends to enlighten the readers regarding rich nutritional profile of the watermelon with special focus on lycopene and its therapeutic aspects like prevent oxidative stress, cancer, hypercholesterolemia, diabetes and macular disorders.
Classification and nutritional profile
Watermelon (Citrullus lanatus) has association with cucumber, pumpkin, squash and gourds; belonging to family Cucurbitaceae (Edwards et al., 2003[37]). Fruit of this plant is major consumed portion and variations in growth characteristics determine its end use quality (Maynard, 2001[79]; Oms-Oliu et al., 2009[93]). Considering the nutritional profile, consumption of 100 g watermelon provides 30 kcal. It contains almost 92 % water and 7.55 % of carbohydrates out of which 6.2 % are sugars and 0.4 % dietary fiber. It is enriched with carotenoid, vitamin C, citrulline, carotenoids and flavonoids and fat and cholesterol free, thus considered as low caloric fruit (Leskovar et al., 2004[69]; Bruton et al., 2009[17]). Additionally, watermelon is rich source of ß-carotene acts as an antioxidant and precursor of vitamin A.
Besides the presence of lycopene, it is a source of B vitamins, especially B1 and B6, as well as minerals such as potassium and magnesium (Huh et al., 2008[50]). Watermelon contains phenolics quite comparable with that of other fruits (Kaur and Kapoor, 2001[63]; Jaskani et al., 2005[55]). It is an inexpensive and nutritious source that is readily available to all socio-economic groups of Pakistan throughout the summer season. Its consumption depends on number of factors e.g. availability, income, age, gender, racial and ethnic norms. In this context, per capita consumption in Asian communities is almost 3 times greater as compared to other part of globe (Dermesonlouoglou et al., 2007[33](Fig. 1)).
Aroma contributing volatiles
In various fruits, flowers and spices monoterpens and norisoprenoids (apocarotenals) are the key compounds producing characteristic scent. In case of watermelon, distinctive aroma is imparted by medium- and short-chain fatty acids along with geranial, ß-ionone and neral that are some of the norisoprenoid and monoterpene compounds. However, esters are absent unlikely as in most fruits i.e. strawberry, banana, melon etc. (Tadmor et al., 2005[111]). In-vitro evidences have supported that fruit scents are degraded carotenoids by the action of lipoxygenases, peroxidases and dioxygenases. However, it is also interesting to know that citral that is an aromatic compound of lemon grass, lemon basil and various lemon scented plants is a combination cis- and trans-monoterpene, neral and geranial. Several gathered information have supported its biosynthesis in lycopene rich fruits as in watermelon and tomato (Micol et al., 2007[81]).
Watermelon: a potential source of lycopene
Earlier, only tomato and its products were considered as potential sources of lycopene but now there are proven facts that watermelon also contains appreciable amount of cis-configured lycopene. Thus consumer is gradually shifting towards watermelon and its allied products for their health concerns. Nevertheless, the quantity of lycopene varies depending upon the variety and growing conditions (Fish and Davis, 2003[41]). Overall, lycopene ranges from 2.30-7.20 mg/100 g fresh weight bases, present in crystalline form in cell (Huh et al., 2008[50]; Chaoensiri et al., 2009[25]; Artes-Henandez et al., 2010[9]). More interestingly, lycopene contents of red fleshed watermelon are almost 40 % higher than tomato i.e. 4.81 and 3.03 mg/100 g, respectively. However, yellow orange and yellow colored fleshed have relatively less lycopene content i.e. 3.68 and 2.51 mg/100 g, respectively (Jaskani, 2005[55]; Choudhary et al., 2009[28]). In tomato, lycopene is available in relatively higher quantity after heat treatment due to break down of protein-carotenoid complex. In contrast, lycopene from watermelon is available directly to the human body just after consumption (Edwards et al., 2003[37]; Perkins-Veaize and Collins, 2004[94]; Jaskani et al., 2006[56]; Saftner et al., 2007[103]).
Storage conditions are also cardinal that significantly affect the concentrations of lycopene, phenolics and vitamin C contents. The higher ratio of lycopene to carotene in watermelon i.e. 1:12 yields remarkable antioxidant capacity (Mort et al., 2008[85]). Owing to this specific characteristic, foods high in lycopene contents are referred as functional foods (Shi and Maguer, 2000[107]; Collins et al., 2005[30]; Jiang and Lin, 2007[59]; Davis et al., 2008[32]).
Synthesis route of lycopene
A complex mechanism persists in the biosynthesis of lycopene that starts when chlorophyll degrades to yield white colored leucoplast thus yielding specialized red color pigmented organelles i.e. chromoplast (Bowen et al., 2002[15]). Lycopene is a carotenoid that is produced as an intermediate product of xanthophylls production; ß-cryptoxanthin, zeaxanthin, leutin etc. Carotenoids are basically formed by 40-C isoprenoids (5-C isoprene unit), called tetraprenoids. A stepwise addition of isopentenyl diphosphate (IPP) takes place with dimethylallyl diphosphate (DMAPP) giving rise 20-C precursor, geranylgeranyl diphosphate (GGPP). On desaturation of GGPP, 11 conjugated double bonds are produced that exist as lycopene in nature. From this point cyclic conversion takes place converting it to α- and ß-carotene that on oxidation produce xanthophylls (Ishida and Bartley, 2005[53]).
Lycopene crystals are in voluminous red color found in the form of small globules suspended throughout the fruit (Chandrika et al., 2009[24]). At cellular level lycopene is present in thylakoid membrane as protein-lycopene complex due to its lipophilic nature. It is well documented that lycopene is present in all-trans form within the fruit that is transformed from cis-configured lycopene due to the action of carotenoid isomerase enzyme. However, in case of watermelon absence of this enzyme keep it in its cis-form (Akhtar et al., 1999[2]; Bangalore et al., 2008[10]).
Lycopene: structure and physicochemical properties
Lycopene is a vibrant tetrapenic carotenoid with molecular formula of C40H56 (Figure 2(Fig. 2)) and contains 11 conjugated and 2 unconjugated double bonds (Fish et al., 2002[42]). It is an acyclic isomer and open-chain analogue of β-carotene that undergoes cis-trans isomerization when interact with light, temperature and chemicals (Ollanketo et al., 2001[90]). A great majority of studies have demonstrated that human blood serum contains both cis- and trans-isomeric forms of lycopene whereas the plants have only trans-configuration except watermelon (Klipstein-Grobusch et al., 2000[65]; Tadmor et al., 2005[111]). Some isomeric forms of lycopene are also depicted in Figure 2(Fig. 2). Among different configurations, 5-cis form is more stable with strong antioxidant potential as compared to all-trans, 7-cis, 9-cis, 11-cis, 13-cis and 15-cis (Arab and Steck, 2000[8]; Chasse et al., 2001[26]; Lewinsohn et al., 2005[71]; Alquézar et al., 2009[4]).
Numerous publications have reported that the amount of lycopene affected significantly as a function of storage time and temperature of watermelon. It has been observed that the lycopene content at storage temperature of 5 °C varied from 7.8 to 8.1 mg/100 g that increased to 8.1 to 12.7 mg/100 g at 20 °C (Mokbe, 2005[84]; Choudhary et al., 2009[28]). Data from various studies have shown an increasing trend of lycopene and β-carotene contents of watermelon at higher storage temperatures. It has been suggested that the carotenoids producing enzymes pathways are sensitive to temperature (Oms-Oliu et al., 2009[92]). The details of physical properties of lycopene are given in Table 1(Tab. 1).
Absorption pathway
Lycopene efficiently absorbs when supplemented with fat owing to its lipophilic characteristics (Rao and Agarwal, 1999[97]). Its assimilation is dependent on chylomicron micells mediated mechanism, facilitates its movement from gastrointestinal tract towards body tissues. The isomeric form of lycopene also affects the absorption e.g. trans-isomeric form is less adsorbed as compared to cis-isomeric configuration (Collins et al., 2005[30]; Rupasinghe and Clegg, 2007[102]). Presences of fat as well as cis-isomeric forms facilitate lycopene absorption afterwards, it resides in the adipose tissues, liver, prostate and adrenal glands. After ingestion of lycopene-based food, disruption carotenoids occur within the low pH environment of stomach where lycopene get attached to the protein to pass through intestinal leumen. The resultant lycopene-protein complex breakdown and lycopene joins chylomicron in blood stream from where it goes to target tissue via hepatic pathway (Jian et al., 2005[57]; Gao et al., 2008[45]). The detailed mechanism of lycopene absorption and its storage is described in Figure 3(Fig. 3).
Lycopene health claims
Lycopene has potential to prevent various chronic ailments like dyslipidemia, diabetes, oncogenesis, neurodegenerative diseases, osteoporosis etc. The protective aspects are ascribed to the singlet oxygen scavenging ability. Numerous metabolic syndromes arise due to high free radicals formation reacting with macromolecules thus oxidizing proteins, lipids and DNA. Lycopene protects humans from various pathogenic attacks responsible for an array of diseases (Ilic and Misso, 2012[52]; Sesso et al., 2005[106]). Several authors have reported that lycopene holds nutraceutical potential and being antioxidant provides protection against free radicals and oxidative damage (Krinsky, 1998[66]; Rao and Agarwal, 1999[97]; Choksi and Joshi, 2007[27]). Free radicals are produced in the body during oxidation reduction reaction however, excessive production deteriorates body defense mechanism, cell membrane and organelles. These degenerative processes resulted in life threatening ailments (Humberto, 2000[51]; Heber and Lu, 2002[47]; Perkins-Veazie and Collins, 2006[95]). The presence of large number of double bonds is responsible for its fairly high free radical scavenging or singlet oxygen quenching ability even better than α- and ß-carotene, lutein and α-tocopherol (Rivero et al., 2001;[101] Perkins-Veazie and Collins, 2004[96]). Lycopene provides protection against degenerative disorders via mechanisms like gap-junction communication, gene function regulation, phase II drug-metabolizing pathways and carcinogenic metabolism (Arab and Steck, 2000[8]; Collins et al., 2004[29]). It has been established through epidemiological studies that lycopene plays a role in maintaining normal cellular differentiation and division (Giovannucci et al., 2002[46]; Choudhary et al., 2009[28]). Lycopene scavenges free radicals at cellular level due to its attachment in cell membrane thereby may prevent hypercholesterolemia and hyperglycemia along with allied dysfunctions (Marinova et al., 2005[77]; Fisher and Frazee, 2006[43]).
a. Oxidative stress
Oxidative stress is an etiological factor in the onset of various metabolic dysfunctions. There are proven facts that uncontrolled oxidation leads to generate excessive reactive oxygen species (ROS), causative agent of many ailments that can address through antioxidants/phytochemicals rich diets (Butt et al., 2009[20]). Excessive production of free radicals leads to atherosclerosis by inactivation of nitric oxide and impairment of endothelium dependent vasodilatation. The ROS are produced continuously in normal metabolic pathways. The diet, smoking, exercises and environmental variables may enhance the production of ROS (Weisburger, 2002[116]; Espin et al., 2007[39]; Migliore and Coppedè, 2009[82]). Despite, antioxidants have ability to start repairing through chain-chain interaction with oxidized biomolecules (Holden et al., 1999[49]; Kauer-Sant'Anna et al., 2009[62]). Diet based therapy indicated a significant role of lycopene in the reduction of oxidative damage of DNA and lymphocytes and short term improvement in LDL oxidation (Alshatwi et al., 2010[5]).
The oxidative balance disrupts during production of reactive oxygen species (ROS) that successively generate double allylic hydrogen atom and initiate oxidation of lipid. Meanwhile, neutrophils catalyze the synthesis of hypochlorous acid that causes oxidative injury in terms of cellular damage. In this milieu, body produces defense enzymes i.e. superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px). Superoxide dismutase acts as first line defense by producing singlet oxygen into hydrogen peroxide. However, GSH-Px and catalase enzymes convert hydrogen peroxide into water. Generally, these enzymes work in harmony but in case of ROS over production, interruption may occur resulting necrosis or apoptosis. In such cases, dietary lycopene acts as a therapeutic agent to combat excessive ROS production (Erdman et al., 2009[38]).
Oxidative stress plays a vital role in the prevalence of chronic diseases. Free radicals are linked with various disease pathogenesis as diabetes, cardiovascular complications, osteoporosis, cancer and cataracts (Ratnam et al., 2006[100]). Lycopene significantly restored the antioxidant enzymes including glutathione peroxidase (GSH-Px), superoxide dismutase (SOD), reduced glutathione (GSH) whilst decreased the levels of lipid peroxide malondialdehyde (MDA) in hypertensive patients (Bose and Agrawal, 2007[14]). Similarly, lycopene was found to be effective in reducing MDA and increasing GSH levels in coronary artery disease (Misra et al., 2006[83]). Later, Kim et al. (2011[64]) examined the effect of lycopene in smoker men with low fruit and vegetable intake through a double blind randomized controlled study. They concluded that lycopene significantly reduces oxidative stress and ameliorates endothelial function (Pennathur et al., 2010[94]).
Likewise, Dogukan et al. (2011[35]) probed lycopene against cisplatin-induced lipid peroxidation and nephrotoxicity in male wistar rats. A significant decrease in renal bax protein was observed in rats administrated on lycopene; an indicator of low oxidative stress. Earlier, Devaraj et al. (2008[34]) determined the response of lycopene supplementation on oxidative stress markers. For the reason, human subjects were provided lycopene for two months following LDL and MDA assessment. Lymphocytes were also analyzed to observe any deleterious effect. Comparison of subjects with lycopene restricted group showed a marked decrease in LDL oxidation and TBAR value i.e. 17 and 21 %, respectively. Previous literature has delineated the protective role of lycopene rich food against DNA damage in normal and cancer cells (Liu et al., 2005[73]; Scolastici et al., 2008[105]). Likewise, a reduction in lipid peroxidation products i.e. TBARS (21 %) and DNA damage markers were observed in the fibroblast of monkey. In case of rats, lycopene injection for five days with a dose level 10 mg/kg/day showed reduction in lipid peroxidation and prostate tissue protection against Fe-induced oxidative damage (Matos et al., 2006[78]).
Various interventional studies have described the interaction between reduced dyslipidemia and lycopene consumption. The lycopene rich diets have potential to reduce lipid peroxidation, one of the leading factors of hypercholesterolemia. In a case study, Mackinnon et al. (2011[75]) noticed an inverse association of dietary lycopene with oxidative stress and positive impact on bone integrity. Effect of no lycopene diet was determined in postmenopausal women of 50 to 60 years. Blood serum was analyzed for protein thiols and thiobarbituric-malondialdehyde reactive substances along with bone turn over markers; alkaline phosphatase and cross-linked N-telopeptide. Inferences of research indicated that dietary restrictions of lycopene for one month resulting tremendous increase in oxidative stress biomarkers with allied bone resorption.
Similarly, a study was conducted in human subjects to find out the role of lycopene enriched functional juice and vitamin C. The core objective was to measure the effect of lycopene (20.6 mg/day) and vitamin C (435 mg/day) against the biomarkers of inflammation and oxidative stress. Blood serum was examined for lipid status, TBAR and antioxidant capacity. The decrease in TBAR (19 to 22 %) and rise in glutathione value (17 to 20 %) was recorded. It has been observed that functional juice led to a decline in total cholesterol (Jacob et al., 2008[54]). A completely randomized cross over study was conducted to probe the role of lycopene in suppression of oxidative stress using lycopene based capsules. Purposely, twelve healthy subjects were administrated on these capsules and a reduction in lipid oxidation was observed. The oxidative stress biomarkers i.e. TBAR and glutathione showed significant changes. The glutathione value raised up to 23.6 %, whereas, a decrease of 20 % in TBAR value was noticed (Rao and Shen, 2002[98]). Lycopene attenuates lifestyle related disorders without imparting any deleterious effects on hematological aspects. Accordingly, Jonker et al. (2003[60]) conducted a three months study to investigate any toxic effect of lycopene in wistar rats. Blood assay was performed to evaluate the red and white blood cell count, hemoglobin, thrombocytes, neutrophils, lymphocytes and monocytes. The summary of hematological aspects revealed non-significant effect of lycopene supplementation. Moreover, histopathological examination did not reflect any adverse sign. The health benefits of lycopene are depicted in Figure 4(Fig. 4).
b. Nutrigenomics and cancer insurgence
Presently, a number of evidences are available indicating direct linkages between food active components and cell genomic with special reference to cancer treatment. Nutrigenomics is a broader term that explains interaction of nutrient with gene expression. Being active dietary component, lycopene interferes at various stages of cancer development i.e. DNA mutation and tumor metastasis thus have direct impact on gene and inhibit mutation (Nahum et al., 2001[88]). However, understanding of lycopene and gene interaction has not yet been well established and needs further research. Lycopene is likely to be associated in the production of phase I and II enzymes that are essential for metabolism of carcinogen within the physiological system. Phase I enzyme has potential to activate the carcinogen whilst phase II enzyme is responsible for attaching polar group to the activated carcinogen that facilitates its excretion. Furthermore, it activates antioxidant response element transcription system within the body to inhibit carcinogenesis, mutagenesis and some other forms of toxicity (Linnewiel et al., 2009[72]; Butt et al., 2013[18]).
Lycopene is a viable antioxidant and beyond this property also attributed for its antiproliferative effects against oncological incidences. Its functionality is associated in diminishing the insulin growth factor thus lowering rate of cancer prevalence. Researchers have unified their opinions on inverse association between blood lycopene level and risk of various cancer types. This individualized approach is also supported by mechanistic exploration with different cell cultures and animal models (Fenko et al., 2009[40]). It has direct relation with phase I and II enzymes and also protects cell membrane, DNA and other macromolecules by reactive oxygen species. Furthermore, it is involved in regression of cancer by interrupting cancer cell growth cycle, apoptosis, hormone regulation and carcinogen metabolism (Butt et al., 2013[18]).
Numerous case studies have indicated chemopreventive role of lycopene regarding aerodigestive tract cancers (oral cavity, pharynx, larynx and esophagus). Accordingly, an oncological efficacy trial was carried out on hamster buccal pouch carcinogenesis induced by 7, 12-dimethylbenzanthracene using lipid peroxidation, glutathione reductase and glutathione S-transferase as biomarkers of chemoprevention. After 2 weeks, biochemical measurements revealed modulating effect of lycopene against buccal pouch cancer and enhancing activities of glutathione redox cycle enzymes (Bhuvaneswari et al., 2001[13]). In a similar study, combined effect of lycopene, vitamin C, flavonoids and phytosterols was established in the regression of aerodigestive tract carcinoma (Stefani et al., 2000[109]).
Colorectal cancer is one of most prevalent malignancy related to colon. Many type of tumorogenesis are accelerated by phosphatidylinositol 3-kinase (PI-3K)/Akt pathway that in turn stimulates transcription and protein translation, essential for cell growth, survival and progression. Cumulative evidences suggested that lycopene could suppress proliferation of colon cancer through modulation of PI-3k. For the purpose, concomitant effect of lycopene and eicosapentaenoic acid (EPA) was determined in human subjects. It was observed that combination of lycopene and EPA inhibit cell growth at higher concentration and somehow reduce at low concentration (Tang et al., 2009[112]). Previous studies have reinforced lycopene association with reduced cancer risk. A case study on colorectal cancer explicated that the patients with colorectal adenomas (a type of polyp proved as precursor of colorectal cancer) had significant lower level of lycopene (35 %) as well as β-carotene (25.5 %) compared to healthy adults. Administration of lycopene at early stages has ability to slow down cancer cell progression (Slattery et al., 2000[108]).
It has been reported from the research in the Harvard University that the subjects consuming appreciable dosage of lycopene have resistance against various cancer lines especially prostrate (Dahan et al., 2008[31]). An inverse correlation exists between the consumption of high lycopene and prostate cancer as observed through a research intervention. Men with high consumption of lycopene in diet reported 25 % less incidences of prostate cancer and overall 44 % reduced risk of other cancers (Tang, 2009[112]). According to Ansari et al. (2004[7]), lycopene therapy has an effective role in the prevention of hormone refractory metastatic prostate cancer. In current frantic incidences of cancer, lycopene must be administrated at early onset of prostate cancer due to its relative innocuous nature rather than chemotherapy and growth factor inhibitors. Afterwards, Kanagaraj et al. (2007[61]) reviewed lycopene impact on the components of insulin growth factors (IGF); found a significant decrease in the proliferation of cells treated with lycopene.
Carcinomas of breast, ovary and endometrium are hormone dependent and have some biological similarities. Numerous epidemiological studies have presumed that diet and nutrition play a preventive role in progression of hormone related cancer milieu. Chalabi et al. (2004[22]) studied breast cancer lines for BRCA1 and BRCA2 for transcription and translation. According to their findings, lycopene dietary sources have direct relation on oncogenesis and developed nutrigenomic link of lycopene. It was hypothesized that lycopene derivatives may act as ligands and regress tumorogenesis. Likewise, females consuming ample amount of watermelon have five times less likely risk of cervical cancer (Rao et al., 2007[99]; Wu et al., 2007[117]; Moussa et al., 2008[86]). The cascade of events is due to high anti-proliferative properties of lycopene as compared to α- and ß- carotene (Levi et al., 2001[70]). Lycopene also hold the ability to control autocrine and paracrine system a contributory factor in the development of the endometrial cancers and malignant tumors (Salman et al., 2007[104]).
c. Cardiovascular complications
Cardiovascular diseases (CVD) is contributed by sedentary lifestyle and reported as a leading cause of mortality. Cardiac risk is elevated due to consumption of high cholesterol diet resulting subacute chronic inflammation. Distinctively, LDL-cholesterol, serum amyloid A (SAA) and inter-cellular adhesion molecule (ICMA-1) are the risk factors thereby facilitate atherosclerosis progression and cardiovascular events (Verschuren et al., 2011[114]).
Hypercholesterolemia is a condition in which serum lipid level increases especially cholesterol and low density lipoproteins (LDL) that further leads to atherosclerosis. Dietary lycopene exert cardio-protective effects due to their high antioxidant activity (Cauza et al., 2004[21]). Apart from lipid lowering drug therapy, dietary interventions are encouraged to attenuate hypercholesterolemia. For the purpose, fifty-six Albino male rats were administrated on tomato lycopene for 10 weeks. The resultant data indicated that the rats fed on hypercholesterolemic diet induced significant increase in serum total lipid level, total cholesterol, low and high density lipoprotein and decreased levels of glutathione peroxidase and malonaldehyde. On the contrary, diet having tomato lycopene mitigated the signs and symptoms of hypercholesterolemia (Basuny et al., 2009[11]). In another research, impact of lycopene was studied on macrophages. The derived results demonstrated that macrophages enrichment with lycopene potentially suppressed cellular cholesterol synthesis and ameliorated macrophages LDL receptor ability. This effect can lead to enhanced clearance of LDL from the plasma thus lycopene is recognized as hypocholesterolemic agent (Fuhrman et al., 1997[44]).
The watermelon is also helpful to lessen some other metabolic syndromes owing to vitamin A, B6, C, magnesium, potassium. These along with lycopene are health promoting functional ingredients associated with reduced risk of cardiovascular disorders. Heart attacks, ischemic strokes and atherosclerosis are faced through the oxidation of low density lipoprotein and their curing has been observed though high consumption of lycopene (Omoni and Aluko, 2005[91]). High intake of lycopene lowered the thickness of the internal layer of the blood vessels thus reducing the risk of myocardial infarction (Zhang and Hamauzu, 2004[118]). Consumption of watermelon is more advantageous as lycopene is readily available through watermelon (Rao and Agarwal, 1999[97]; Weisburger, 2002[116]).
d. Diabetes mellitus
Numerous experimental studies and surveys have indicated that patients with hyperglycemia are more prone towards the risk of coronary complications. In this context, elevated oxidative stress and LDL oxidation are the major contributory factors. High glycemic diet significantly elevates glucose and its auto-oxidation consequently generates free radicals and cell damage (Micol et al., 2007[81]). Besides, Sugiura et al. (2006[110]) explored phenolics i.e. lycopene, lutein, ß-carotene, ß-cryptoxanthin and ß-carotene for their hypoglycemic action. The upshots of the research showed an inverse association of carotenoids with serum aminotransferases in hyperglycemic subjects. Among all, lycopene is proved as deterrent constituent against serum aminotransferases and significantly prevents the onset of hyperglycemia. Additionally, oxidative stress is increased during hyperglycemia phase through intracellular reactive oxygen species (ROS). As a result of this imbalance inside the cell ROS damages the mitochondria, DNA, lipids and other organelles leading to apoptosis. Investigation of Micol et al. (2007[81]) also proved hypoglycemic perspectives of lycopene and elucidated that watermelon lycopene extract significantly improves lipid and glycemic metabolism.
Recent research studies have marked obesity and diabetes as the major public health problems in most of the countries. The diabetes prevalence is so high and estimated that its level raised from 135 to 300 million by the years 1995 to 2025 (American Diabetes Association, 2007[6]). During the progression of obesity, adipokines (cytokines and chimiokines) are synthesized that play an important role in general body physiology. Massive development of adipose tissue leads to inflammation resulting from the excessive production of chimiokines and cytokines thus leading to type II diabetes. Lycopene is a lipophilic carotenoid stored in adipose tissues thereby reduces the pathologies linked with obesity and hyperglycemic conditions (Madhava et al., 2011[76]).
The lycopene based functional drinks have potential to reduce malignant transformation of oxidized cholesterol in diabetic state. The lycopene decreases diabetes in linear fashion by managing glucose abnormalities. Lycopene owes ability to decrease body glucose and raise insulin level in type II diabetes. In an investigation, Jian et al. (2008[58]) studied the impact of oral supplementation of lycopene in normal rats for twenty eight days. The lycopene was daily supplied in doses as 0, 200, 500 and 2000 mg/kg body weight by gavage. No significant signs of abnormality were noticed for hematology, urinalysis and organs weight. However, a decline in glucose value was observed at higher lycopene dose. The significant differences in body glucose were noted between control and lycopene treated rats i.e. 205.6 ± 44.3 and 132.1 ± 35.9 mg/dL, respectively. Conclusively, they confirmed lycopene as an ameliorating factor for hyperglycemia.
Alongside, substantial studies have revealed negative association of hyperglycemia with the central nervous system (CNS), leads to cognitive dysfunction. High intracellular glucose level induces learning and memory impairments and neurochemical and structural abnormalities. In a rat modeling, provision of lycopene supplemented diet ameliorates cholinergic dysfunction, cognitive deficit nitric oxide and reduces oxidative stress. Moreover, a marked decline in serum glucose level was observed i.e. 5 % after 4 mg/day supplementation of lycopene (Kuhad et al., 2008[67]). Clinical findings also delineated lycopene a good option for the development of functional foods owing to its hypoglycemic perspectives. In this context, Mellert et al. (2002[80]) conducted a thirteen days study on normal wistar rats to judge the lycopene response. They deduced that lycopene interim supplementation significantly reduces body glucose level i.e. 13 %.
Watermelon extract is considered as a concentrated source of nutrients along with lycopene. In a trial, 1 % extract was administered to the diabetic rats. At the termination of study, rise in insulin level 37 % whilst decline in glucose 33 % were observed. The study indicated watermelon extract as a hyperinsulinemic and hypoglycemic product (Ahn et al., 2011[1]). In a nested case control trial, data were collected for diabetic middle aged women from a period of 1992 to 2003 to find out the association of dietary lycopene intake with insulin level. During ten years of follow up, observed cases depicted a linear correlation between lycopene and insulin level and a rise of 37-45 % was noticed. The wide range of variations was attributed to the altered body metabolism of diabetic patients. The findings reflected lycopene ability to improve insulin sensitivity and glucose metabolism (Wang et al., 2006[115]).
There are some convincing epidemiological evidences in favor of lycopene, vitamin E and vitamin C with decreased incidence of cardiovascular complications in diabetic patients. Accordingly, a study was conducted by Upritchard et al. (2000[113]) to determine the effect of lycopene and vitamin E and C on LDL oxidation and inflammatory activity in type II diabetes. Initially, 57 diabetic patients received functional juice as a source of dietary lycopene (500 mL/day) along with vitamin E (800 U/day) and vitamin C (500 mg/day). The results indicated that high intake of lycopene and vitamin C and E are one of the options to reduce various coronary complications in diabetic patients. Likewise, lycopene dose dependent effect was estimated in streptozotocin (STZ) induced hyperglycemic rats to find its potential against hyperglycemia, hyperlipidemia and abnormal antioxidant status. Furthermore, results were compared with hyperglycemic and normoglycemic rat groups. A dose dependent decrease in glucose level and TBAR along with rise in insulin value was noticed. The investigation elucidated antidiabetic activity of lycopene by lowering free radicals (Ali and Agha, 2009[3]).
Diabetes based neuronal abnormalities are attributed to the high intracellular glucose. Effect of lycopene was determined with special reference to its antioxidative and anti-inflammatory behavior on oxidative stress, cognitive function and inflammation in streptozotocin (STZ) induced diabetic rats. During the ailment, acetyl cholinesterase activity, a biomarker of cholinergic dysfunction increased in cerebral cortex of diabetic rats about 1.8 fold. Moreover, a rise in thiobarbituric acid reactive substances was about 2 folds. It was concluded that lycopene has ability to mitigate cognitive deficit, inflammation and oxidative stress in diabetic rats (Kuhad et al., 2008[67]).
Hyperalgesia is a neuropathic pain in diabetes because of microvascular complications. An investigation performed by Kuhad et al. (2008[67]) has revealed the therapeutic role of watermelon lycopene against neuropathic pain associated with diabetes. Additionally, lycopene has ability to reverse the hyperalgesic stage to some extent. Similarly, role of lycopene as an antioxidant was assessed in streptozotocin (STZ) induced diabetic rats, In this regard, 6 female rats received 10 mg/kg body weight lycopene once a day for three weeks. Diabetes induction caused significant rise in serum glucose and reduction in body weight. However, lycopene showed assuaging effect on diabetic rats by reducing serum glucose level up to 25 %. Weight loss was also prevented after two weeks of lycopene administration. Conclusively, lycopene supplementation proved valuable to combat against hyperglycemia (Duzguner et al., 2008[36]).
e. Macular diseases
Macular degenerative disease onsets with the thinning of macula layer of retina thereby resulting in gradual decrease in vision. The symptoms include appearance of yellow spots (Bramley, 2000[16]). There are two types of age related macular degeneration (AMD) including wet and dry. However, dry AMD is more prevalent further in turns to wet AMD when new blood vessels develop to reduce the dryness of macular layer. The development of such vessels favors hemorrhage, swelling, and scar on the eye tissue (Bazzano et al., 2002[12]). The utilization of carotenoids or their rich sources can reduce the risk of macular and other degenerative disorders. In an experimental study of macula-degeneration, subjects with low lycopene-serum concentrations were at high risk. Lycopene is also effective against immunodeficiency diseases like HIV and cerebral damage microangiopathy in Austrian stroke (Kun et al., 2006[68]).
Conclusions
Watermelon is a proven distinctive source of lycopene claiming new era vitamin due to health promising properties. Diversified nature of watermelon lycopene has attained core attention of researchers in terms of bioavailability and absorption. Safe and sound extraction procedure with minimal loss is desirable at industrial scale. Finally, available information from numerous cell culture and animal models have illuminated the therapeutic role of lycopene against life threatening metabolic syndromes like oxidative stress, cancer, CVD, diabetes etc. Nevertheless, still there is a need for dietary intervention for better understanding of role of lycopene on human health.
References
- 1.Ahn J, Choi W, Kim S, Ha T. Anti-diabetic effect of watermelon (Citrullus vulgaris Schrad) on Streptozotocin-induced diabetic mice. Food Sci Biotechnol. 2011;20:251–254. [Google Scholar]
- 2.Akhtar MS, Goldschmidt EE, John I, Rodoni S, Matile P, Grierson, D Altered patterns of senescence and ripening in gf, a stay-green mutant of tomato (Lycopersicon esculentum Mill.) J Exp Bot. 1999;50:1115–1122. [Google Scholar]
- 3.Ali MM, Agha FG. Amelioration of streptozotocin-induced diabetes mellitus, oxidative stress and dys-lipidemia in rats by tomato extract lycopene. Scandinavian J Clin Lab Invest. 2009;69:371–379. doi: 10.1080/00365510802658473. [DOI] [PubMed] [Google Scholar]
- 4.Alquézar B, Zacarías L, Rodrigo MJ. Molecular and functional characterization of a novel chromoplast-specific lycopene β-cyclase from Citrus and its relation to lycopene accumulation. J Exp Bot. 2009;60:1783–1797. doi: 10.1093/jxb/erp048. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Alshatwi AA, Al Obaaid MA, Al Sedairy SA, Al-Assaf AH, Zhang JJ, Lei KY. Tomato powder is more protective than lycopene supplement against lipid peroxidation in rats. Nutr Res. 2010;30:66–73. doi: 10.1016/j.nutres.2009.12.002. [DOI] [PubMed] [Google Scholar]
- 6.American Diabetes Association. Standards of medical care for diabetes. Diabetes Care. 2007;17:1514–1522. [Google Scholar]
- 7.Ansari MS, Gupta NP. Lycopene: a novel drug therapy in hormone refractory metastatic prostate cancer. Urol Oncol: Semin Orig Invest. 2004;22:415–420. doi: 10.1016/j.urolonc.2004.05.009. [DOI] [PubMed] [Google Scholar]
- 8.Arab L, Steck S. Lycopene and cardiovascular disease. Am J Clin Nutr. 2000;71:1691S–1695S. doi: 10.1093/ajcn/71.6.1691S. [DOI] [PubMed] [Google Scholar]
- 9.Artés-Hernández F, Robles PA, Gómez PA, Tomás-Callejas A, Artés F. Low UV-C illumination for keeping overall quality of fresh-cut watermelon. Postharvest Biol Tec. 2010;55:114–120. [Google Scholar]
- 10.Bangalore DV, McGlynn WG, Scott DD. Effects of fruit maturity on watermelon ultrastructure and intracellular lycopene distribution. J Food Sci. 2008;73:S222–S228. doi: 10.1111/j.1750-3841.2008.00778.x. [DOI] [PubMed] [Google Scholar]
- 11.Basuny AM, Gaafar AM, Arafat SM. Tomato lycopene is a natural antioxidant and can alleviate hypercholesterolemia. Afr J Biotechnol. 2009;8:6627–6633. [Google Scholar]
- 12.Bazzano LA, He J, Ogden LG, Loria CM, Vupputuri S, Myers L, et al. Fruit and vegetable intake and risk of cardiovascular disease in US adults: the first National Health and Nutrition Examination Survey Epidemiologic Follow-up Study. Am J Clin Nutr. 2002;76:93–99. doi: 10.1093/ajcn/76.1.93. [DOI] [PubMed] [Google Scholar]
- 13.Bhuvaneswari V, Velmurugan B, Balasenthil S, Ramachandran CR, Nagini S. Chemopreventive efficacy of lycopene on 7,12-dimethylbenz[a]anthracene-induced hamster buccal pouch carcinogenesis. Fitoterapia. 2001;72:865–874. doi: 10.1016/s0367-326x(01)00321-5. [DOI] [PubMed] [Google Scholar]
- 14.Bose KSC, Agrawal BK. Effect of lycopene from tomatoes (cooked) on plasma antioxidant enzymes, lipid peroxidation rate and lipid profile in grade-I hypertension. Ann Nutr Metab. 2007;51:477–481. doi: 10.1159/000111170. [DOI] [PubMed] [Google Scholar]
- 15.Bowen P, Chen L, Stacewicz-Sapuntzakis M, Duncan C, Sharifi R, Ghosh L, et al. Tomato sauce supplementation and prostate cancer: lycopene accumulation and modulation of biomarkers of carcinogenesis. Exp Biol Med. 2002;227:886–893. doi: 10.1177/153537020222701008. [DOI] [PubMed] [Google Scholar]
- 16.Bramley PM. Is lycopene beneficial to human health? Phytochemistry. 2000;54:233–236. doi: 10.1016/s0031-9422(00)00103-5. [DOI] [PubMed] [Google Scholar]
- 17.Bruton BD, Fish WW, Roberts W, Popham TW. The influence of rootstock selection on fruit quality attributes of watermelon. Open Food Sci J. 2009;3:15–34. [Google Scholar]
- 18.Butt MS, Naz A, Sultan MT, Qayyum MMN. Anti-oncogenic perspectives of spices/herbs: a comprehensive review. EXCLI J. 2013;12:1043–1065. [PMC free article] [PubMed] [Google Scholar]
- 19.Butt MS, Nazir A, Sultan MT, Schoren K. Morus alba L. nature’s functional tonic. Trends Food Sci Technol. 2008;19:505–512. [Google Scholar]
- 20.Butt MS, Sultan MT, Butt MS, Iqbal J. Garlic: Nature’s protection against physiological threats. Crit Rev Food Sci Nutr. 2009;49:538–551. doi: 10.1080/10408390802145344. [DOI] [PubMed] [Google Scholar]
- 21.Cauza E, Jansen M, Resch U, Dunky A, Derfler K, Winklhofer-Roob BM, et al. Effects of LDL-immuno-apheresis on plasma concentration of vitamin E and carotenoids in patients with familial hypercholestrolemia. J Clin Apheresis. 2004;19:174–179. doi: 10.1002/jca.20026. [DOI] [PubMed] [Google Scholar]
- 22.Chalabi N, Corre LL, Maurizis J-C, Bignon Y-J, Bernard-Gallon DJ. The effects of lycopene on the proliferation of human breast cell and BRAC1v and BRAC2 gene expression. Eur J Cancer. 2004;40:1768–1775. doi: 10.1016/j.ejca.2004.03.028. [DOI] [PubMed] [Google Scholar]
- 23.Chalabi N, Delort L, LeCorre L, Satib S, Bignon J, Bernard-Gallon D. Gene signature of breast cancer cell lines treated with lycopene. Pharmacogenomics. 2006;7:663–72. doi: 10.2217/14622416.7.5.663. [DOI] [PubMed] [Google Scholar]
- 24.Chandrika UG, Fernando KSSP, Ranaweera KKDS. Carotenoid content and in vitro bioaccessibility of lycopene from guava (Psidium guajava) and watermelon (Citrullus lanatus) by high-performance liquid chromatography diode array detection. Int J Food Sci Nutr. 2009;60:558–566. doi: 10.3109/09637480801987195. [DOI] [PubMed] [Google Scholar]
- 25.Charoensiri R, Kongkachuichai R, Suknicom S, Sungpuag P. Beta-carotene, lycopene, and alpha-tocopherol contents of selected Thai fruits. Food Chem. 2009;113:202–207. [Google Scholar]
- 26.Chasse GA, Mak ML, Deretey E, Farkas I, Torday LL, Papp JG, et al. An ab initio computational study on selected lycopene isomers. J Mol Struct. 2001;571:27–37. [Google Scholar]
- 27.Choksi PM, Joshi CVY. A review on lycopene-extraction, purification, stability and applications. Int J Food Prop. 2007;10:289–298. [Google Scholar]
- 28.Choudhary R, Bowser TJ, Weckler P, Maness NO, McGlynn W. Rapid estimation of lycopene concentration in watermelon and tomato puree by fiber optic visible reflectance spectroscopy. Postharvest Biol Technol. 2009;52:103–109. [Google Scholar]
- 29.Collins JK, Arjamndi BH, Claypool PL, Perkins-Veazie P, Baker RA, Clevidence BA. Lycopene from two food sources does not affect antioxidant or cholesterol status of middle-aged adults. J Food Agric. 2004;2:1–7. doi: 10.1186/1475-2891-3-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Collins JK, Davis AR, Adams A, Perkins-Veazie P. Sensory evaluation of low sugar watermelon by consumers. Hort Sci. 2005;40:883. [Google Scholar]
- 31.Dahan K, Fennal M, Kumar NB. Lycopene in the protection of prostate cancer. J Soc Integrat Oncol. 2008;2:29–36. [PubMed] [Google Scholar]
- 32.Davis AR, Webber CL, 3rd, Perkins-Veazie P, Ruso V, Lopez Galarza S, Sakata Y. A review of production systems on watermelon quality. In: Pitrat M, editor. Cucurbitaceae. Proceedings of the IXth EUCARPIA meeting on genetics and breeding of Cucurbitaceae, Avignon (France), May 21-24th. 2008. pp. 515–520. [Google Scholar]
- 33.Dermesonlouoglou E, Giannakourou M, Taoukis P. Kinetic modelling of the quality degradation of frozen watermelon tissue: effect of the osmotic dehydration as a pretreatment. Int J Food Sci Technol. 2007;42:790–798. [Google Scholar]
- 34.Devaraj S, Mathur S, Basu A, Aung HH, Vasu VT, Meyers S, et al. A dose-response study on the effects of purified lycopene supplementation on biomarkers of oxidative stress. J Am Coll Nutr. 2008;27:267–273. doi: 10.1080/07315724.2008.10719699. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Dogukan A, Tuzcu M, Agca CA, Gencoglu H, Sahin N, Onderci M, et al. A tomato lycopene complex protects the kidney from cisplatin-induced injury via affecting oxidative stress as well as Bax, Bcl-2, and HSPs expression. Nutr Can. 2011;63:427–434. doi: 10.1080/01635581.2011.535958. [DOI] [PubMed] [Google Scholar]
- 36.Duzguner V, Kucukgul A, Erdogan S, Celik S, Sahin K. Effect of lycopene administration on plasma glucose, oxidative stress and body weight in streptozotocin diabetic rats. J Appl Anim Res. 2008;33:17–20. [Google Scholar]
- 37.Edwards AJ, Vinyard BT, Wiley ER, Brown ED, Collins JK, Perkins-Veazie P, et al. Consumption of watermelon juice increases plasma concentrations of lycopene and β-carotene in humans. J Nutr. 2003;133:1043–1050. doi: 10.1093/jn/133.4.1043. [DOI] [PubMed] [Google Scholar]
- 38.Erdman JW, Ford NA, Lindshield BL. Are the health attributes of lycopene related to its antioxidant function? Arch Biochem Biophys. 2009;483:229–235. doi: 10.1016/j.abb.2008.10.022. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Espin JC, Garcia-Conesa MT, Tomas-Barberan FA. Nutraceuticals: facts and fiction. Phytochemistry. 2007;68:2986–3008. doi: 10.1016/j.phytochem.2007.09.014. [DOI] [PubMed] [Google Scholar]
- 40.Fenko A, Schifferstein HN, Huang TC, Hekkert P. What makes products fresh: The smell or the colour? Food Qual Prefer. 2009;20:372–379. [Google Scholar]
- 41.Fish WW, Davis AR. The effects of frozen storage conditions on lycopene stability in watermelon tissue. J Agric Food Chem. 2003;51:3582–3585. doi: 10.1021/jf030022f. [DOI] [PubMed] [Google Scholar]
- 42.Fish WW, Perkins-Veazie P, Collins JK. A quantitative assay for lycopene that utilizes reduced volumes of organic solvents. J Food Compost Anal. 2002;15:309–317. [Google Scholar]
- 43.Fisher J, Frazee LA. Update on prostate cancer chemoprevention. J Hum Pharmacol Drug Ther. 2006;26:353–359. doi: 10.1592/phco.26.3.353. [DOI] [PubMed] [Google Scholar]
- 44.Fuhrman B, Elis A, Aviram M. Hypocholesterolemic effect of lycopene and ß-carotene is related to suppression of cholesterol synthesis and augmentation of LDL receptor activity in macrophages. Biochem Biophys Res C. 1997;233:658–662. doi: 10.1006/bbrc.1997.6520. [DOI] [PubMed] [Google Scholar]
- 45.Gao H, Zhu H, Shao Y, Chen A, Lu C, Zhu B, et al. Lycopene accumulation affects the biosynthesis of some carotenoid‐related volatiles independent of ethylene in tomato. J Integrat Plant Biol. 2008;50:991–996. doi: 10.1111/j.1744-7909.2008.00685.x. [DOI] [PubMed] [Google Scholar]
- 46.Giovannucci E, Rimm EB, Liu Y, Stampfer MJ, Willett WC. A prospective study of tomato products, lycopene, and prostate cancer risk. J Natl Cancer Inst. 2002;94:391–398. doi: 10.1093/jnci/94.5.391. [DOI] [PubMed] [Google Scholar]
- 47.Heber D, Lu QY. Overview of mechanisms of action of lycopene. Exp Biol Med. 2002;227:920–923. doi: 10.1177/153537020222701013. [DOI] [PubMed] [Google Scholar]
- 48.Helyes L, Lugasi A, Pogonyi A, Pék Z. Effect of variety and grafting on lycopene content of tomato (Lycopersicon lycopersicum L. Karsten) fruit. Acta Aliment. 2009;38:27–34. [Google Scholar]
- 49.Holden JM, Eldridge AL, Beecher GR, Buzzard IM, Bhagwat AS, Davis CS, et al. Carotenoid content of U.S. foods: An update of the database. J Food Compos Anal. 1999;12:169–196. [Google Scholar]
- 50.Huh YC, Solmaz I, Sari N. Morphological characterization of Korean and Turkish watermelon germplasm. In: Pitrat M, editor. Cucurbitaceae. Proceedings of the IXth EUCARPIA meeting on genetics and breeding of Cucurbitaceae, Avignon (France), May 21-24th. 2008. pp. 327–333. [Google Scholar]
- 51.Humberto BJ, Churchill T, Malfair D, Wessler A, Jewell LD, Parsons HG, et al. Inhibition of poly (ADP-ribose) polymerase attenuates inflammation in a model of chronic colitis. Am J Pharm. 2000;279:G641–G651. doi: 10.1152/ajpgi.2000.279.3.G641. [DOI] [PubMed] [Google Scholar]
- 52.Ilic D, Misso M. Lycopene for the prevention and treatment of benign prostatic hyperplasia and prostate cancer: A systematic review. Maturitas. 2012;72:269–276. doi: 10.1016/j.maturitas.2012.04.014. [DOI] [PubMed] [Google Scholar]
- 53.Ishida BK, Bartley GE. Carotenoids: chemistry, sources, and physiology. In: Caballero B, Allen L, Prentice A, editors. Encyclopedia of human nutrition. 2nd ed. Vol. 1. Amsterdam: Elsevier; 2005. pp. 330–338. [Google Scholar]
- 54.Jacob K, Periago MJ, Bohm V, Berruezo GR. Influence of lycopene and vitamin C from juice on biomarkers of oxidative stress and inflammation. Brit J Nutr. 2008;99:137–146. doi: 10.1017/S0007114507791894. [DOI] [PubMed] [Google Scholar]
- 55.Jaskani MJ, Kwon SW, Kim DH. Comparative study on vegetative, reproductive and qualitative traits of seven diploid and tetraploid watermelon lines. Euphytica. 2005;145:259–268. [Google Scholar]
- 56.Jaskani MJ, Kwon SW, Kim DH, Abbas H. Seed treatments and orientation affects germination and seedling emergence in tetraploid watermelon. Pak J Bot. 2006;38:89. [Google Scholar]
- 57.Jian L, Du CJ, Lee AH, Binns CW. Do dietary lycopene and other carotenoids protect against prostate cancer? Int J Cancer. 2005;113:1010–1014. doi: 10.1002/ijc.20667. [DOI] [PubMed] [Google Scholar]
- 58.Jian W, Chiou MH, Chen YT, Lin CN, Wub MC, Du CJ, et al. Twenty-eight-day oral toxicity study of lycopene from recombinant Escherichia coli in rats. Regul Toxicol Pharmacol. 2008;52:163–168. doi: 10.1016/j.yrtph.2008.08.011. [DOI] [PubMed] [Google Scholar]
- 59.Jiang XT, Lin DP. Discovery of watermelon gynoecious gene gy. Acta Hortic Sin. 2007;1:027. [Google Scholar]
- 60.Jonker D, Kuper CF, Fraile N, Estrella A, Rodriguez OC. Ninety-day oral toxicity study of lycopene from Blakeslea trispora in rats. Regul Toxicol Pharmacol. 2003;37:396–406. doi: 10.1016/s0273-2300(03)00013-8. [DOI] [PubMed] [Google Scholar]
- 61.Kanagaraj P, Vijayababu MR, Ravisankar B, Anbalagan J, Aruldhas MM, Arunakaran J. Effect of lycopene on insulin-like growth factor-I, IGF binding protein-3 and IGF type-I receptor in prostate cancer cells. J Cancer Res Clin Oncol. 2007;133:351–359. doi: 10.1007/s00432-006-0177-6. [DOI] [PubMed] [Google Scholar]
- 62.Kauer-Sant'Anna M, Kapczinski F, Andreazza AC, Bond DJ, Lam RW, Young LT, et al. Brain-derived neurotrophic factor and inflammatory markers in patients with early-vs. late-stage bipolar disorder. Int J Neuropsychopharmacol. 2009;12:447–458. doi: 10.1017/S1461145708009310. [DOI] [PubMed] [Google Scholar]
- 63.Kaur C, Kapoor HC. Antioxidants in fruits and vegetables – the millennium’s health. Int J Food Sci Technol. 2001;36:703–725. [Google Scholar]
- 64.Kim JI, Paik JK, Kim OY, Park HW, Lee JH, Jang Y, et al. Effects of lycopene supplementation on oxidative stress and markers of endothelial function in healthy men. Atherosclerosis. 2011;215:189–195. doi: 10.1016/j.atherosclerosis.2010.11.036. [DOI] [PubMed] [Google Scholar]
- 65.Klipstein-Grobusch K, Launer L, Geleijnse JM, Boeing H, Hofman A, Witteman JCM. Serum carotenoids and atherosclerosis: the Rotterdam Study. Atherosclerosis. 2000;148:49–56. doi: 10.1016/s0021-9150(99)00221-x. [DOI] [PubMed] [Google Scholar]
- 66.Krinsky NI. Overview of lycopene, carotenoids and disease prevention. Exp Biol Med. 1998;218:95–97. doi: 10.3181/00379727-218-44273. [DOI] [PubMed] [Google Scholar]
- 67.Kuhad A, Sharma S, Chopra K. Lycopene attenuates thermal hyperalgesia in a diabetic mouse model of neuropathic pain. Eur J Pain. 2008;12:624–632. doi: 10.1016/j.ejpain.2007.10.008. [DOI] [PubMed] [Google Scholar]
- 68.Kun Y, Ssonko Lule U, Xiao-Lin D. Lycopene: Its properties and relationship to human health. Food Rev Int. 2006;22:309–333. [Google Scholar]
- 69.Leskovar DI, Bang H, Crosby KM, Maness N, Franco JA, Perkins-Veazie P. Lycopene, carbohydrates, ascorbic acid and yield components of diploid and triploid watermelon cultivars are affected by deficit irrigation. J Hortic Sci Biotechnol. 2004;79:75–81. [Google Scholar]
- 70.Levi A, Thomas CE, Keinath AP, Wehner TC. Genetic diversity among watermelon (Citrullus lanatus and Citrullus colocynthis) accessions. Genet Resour Crop Ev. 2001;48:559–566. [Google Scholar]
- 71.Lewinsohn E, Sitrit Y, Bar E, Azulay Y, Ibdah M, Meir A, et al. Not just colors - carotenoid degradation as a link between pigmentation and aroma in tomato and watermelon fruit. Trends Food Sci Technol. 2005;16:407–415. [Google Scholar]
- 72.Linnewiel, K, Ernst H, Caris-Veyrat C, Ben-Dor A, Kampf A, Salman H, et al. Structure activity relationship of carotenoid derivatives in activation of the electrophile/antioxidant response element transcription system. Free Radic Biol Med. 2009;47:659–667. doi: 10.1016/j.freeradbiomed.2009.06.008. [DOI] [PubMed] [Google Scholar]
- 73.Liu CC, Huang CC, Lin WT, Hsieh CC, Huang SY, Lin SJ, et al. Lycopene supplementation attenuated xanthine oxidase and myeloperoxidase activities in skeletal muscle tissues of rats after exhaustive exercise. Brit J Nutr. 2005;94:595–601. doi: 10.1079/bjn20051541. [DOI] [PubMed] [Google Scholar]
- 74.Lucier G, Lin B-H USDA, United States Department of Agriculture, editor. Vegetables and specialties: situation and outlook report. United States Department of Agriculture; 2001. Factors affecting watermelon consumption in the United States; pp. 23–29. (VGS-287). [Google Scholar]
- 75.Mackinnon ES, Rao AV, Rao LG. Dietary restriction of lycopene for a period of one month resulted in significantly increased biomarkers of oxidative stress and bone resorption in postmenopausal women. J Nutr Health Aging. 2011;15:133–138. doi: 10.1007/s12603-011-0026-4. [DOI] [PubMed] [Google Scholar]
- 76.Madhava RA, Banji D, Banji OJF, Kumar K, Ragini M. Lycopene and its importance in treating various diseases in human. Int Res J Pharm. 2011;2:31–37. [Google Scholar]
- 77.Marinova D, Ribarova F, Atanassova M. Total phenolics and total flavonoids in Bulgarian fruits and vegetables. J Univ Chem Technol Metallurgy. 2005;40:255–260. [Google Scholar]
- 78.Matos HR, Marques SA, Gomes OF, Silva AA, Heimann JC, Di Mascio P, et al. Lycopene and ß-carotene protect in vivo iron-induced oxidative stress damage in rat prostate. Braz J Med Biol Res. 2006;39:203–210. doi: 10.1590/s0100-879x2006000200006. [DOI] [PubMed] [Google Scholar]
- 79.Maynard DN. Watermelons: characteristics, production, and marketing. Alexandria, VA: ASHS Press; 2001. [Google Scholar]
- 80.Mellert W, Deckardt K, Gembardt C, Schultea S, Van Ravenzwaay B, Slesinski RS. Thirteen-week oral toxicity study of synthetic lycopene products in rats. Food Chem Toxicol. 2002;40:1581–1588. doi: 10.1016/s0278-6915(02)00113-8. [DOI] [PubMed] [Google Scholar]
- 81.Micol V, Larson H, Edeas B, Ikeda T. Watermelon extract stimulates antioxidant enzymes and improves glycemic and lipid metabolism. Agro Food Industry Hi-Tech. 2007;18:22–26. [Google Scholar]
- 82.Migliore L, Coppedè F. Environmental-induced oxidative stress in neurodegenerative disorders and aging. Mutat Res. 2009;674:73–84. doi: 10.1016/j.mrgentox.2008.09.013. [DOI] [PubMed] [Google Scholar]
- 83.Misra R, Mangi S, Joshi S, Mittal S, Gupta SK, Pandey RM. LycoRed as an alternative to hormone replacement therapy in lowering serum lipids and oxidative stress markers: a randomized controlled clinical trial. J Obstet Gynaecol Res. 2006;32:299–304. doi: 10.1111/j.1447-0756.2006.00410.x. [DOI] [PubMed] [Google Scholar]
- 84.Mokbe MS, Hashinaga F. Antibacterial and antioxidant activities of banana (Musa, AAA cv. Cavendish) fruits peel. Am J Biochem Biotechnol. 2005;1:125. [Google Scholar]
- 85.Mort A, Zheng Y, Qiu F, Nimtz M, Bell-Eunice G. Structure of xylogalacturonan fragments from watermelon cell-wall pectin. Endopolygalacturonase can accommodate a xylosyl residue on the galacturonic acid just following the hydrolysis site. Carbohydr Res. 2008;343:1212–1221. doi: 10.1016/j.carres.2008.03.021. [DOI] [PubMed] [Google Scholar]
- 86.Moussa M, Landrier JF, Reboul E, Ghiringhelli O, Coméra C, Collet X, et al. Lycopene absorption in human intestinal cells and in mice involves scavenger receptor class B type I but not Niemann-Pick C1-like 1. J Nutr. 2008;138:1432–1436. doi: 10.1093/jn/138.8.1432. [DOI] [PubMed] [Google Scholar]
- 87.Mutanen M, Pajari A-M. Diet and cancer. Vol. 2. Dordrecht Springer; 2011. Vegetables, whole grains, and their derivatives in cancer prevention. [Google Scholar]
- 88.Nahum A, Hirsch K, Danilenko M. Lycopene inhibition of cell cycle progression in breast and endometrial cancer cells is associated with reduction in cyclin D levels and retention of p27(Kip1) in the cyclin E-cdk2 complexes. Oncogene. 2001;20:3428–36. doi: 10.1038/sj.onc.1204452. [DOI] [PubMed] [Google Scholar]
- 89.Naz A, Butt MS, Pasha I, Nawaz H. Antioxidant indices of watermelon juice and lycopene extract. Pak J Nutr. 2013;12:255–260. [Google Scholar]
- 90.Ollanketo M, Hartonen K, Riekkola ML, Holm Y, Hiltunen R. Supercritical carbon dioxide extraction of lycopene in tomato skins. Euro Food Res Technol. 2001;212:561–565. [Google Scholar]
- 91.Omoni AO, Aluko RE. The anti-carcinogenic and anti-atherogenic effects of lycopene: a review. Trends Food Sci Technol. 2005;16:344–350. [Google Scholar]
- 92.Oms-Oliu G, Odriozola-Serrano I, Soliva-Fortuny R, Martín-Belloso O. Effects of high-intensity pulsed electric field processing conditions on lycopene, vitamin C and antioxidant capacity of watermelon juice. Food Chem. 2009;115:1312–1319. [Google Scholar]
- 93.Oms-Oliu G, Odriozola-Serrano I, Soliva-Fortuny R, Martín-Belloso O. Use of Weibull distribution for describing kinetics of antioxidant potential changes in fresh-cut watermelon. J Food Eng. 2009;95:99–105. [Google Scholar]
- 94.Pennathur S, Maitra D, Byun J, Sliskovic I, Abdulhamid I, Saed GM, et al. Potent antioxidative activity of lycopene: A potential role in scavenging hypochlorous acid. Free Radic Biol Med. 2010;49:205–213. doi: 10.1016/j.freeradbiomed.2010.04.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 95.Perkins-Veazie P, Collins JK. Carotenoid changes of intact watermelons after storage. J Agric Food Chem. 2006;54:5868–5874. doi: 10.1021/jf0532664. [DOI] [PubMed] [Google Scholar]
- 96.Perkins-Veazie P, Collins JK. Flesh quality and lycopene stability of fresh-cut watermelon. Postharvest Biol Technol. 2004;31:159–166. [Google Scholar]
- 97.Rao AV, Agarwal S. Role of lycopene as antioxidant carotenoid in the prevention of chronic diseases: a review. Nutr Res. 1999;19:305–323. [Google Scholar]
- 98.Rao AV, Shen H. Effect of low dose lycopene intake on lycopene bioavailability and oxidative stress. Nutr Res. 2002;22:1125–1131. [Google Scholar]
- 99.Rao LG, Mackinnon ES, Josse RG, Murray TM, Strauss A, Rao AV. Lycopene consumption decreases oxidative stress and bone resorption markers in postmenopausal women. Osteoporosis Int. 2007;18:109–115. doi: 10.1007/s00198-006-0205-z. [DOI] [PubMed] [Google Scholar]
- 100.Ratnam DV, Ankola DD, Bhardwaj V, Sahana DK, Kumar MNV. Role of antioxidants in prophylaxis and therapy: A pharmaceutical perspective. J Control Release. 2006;113:189–207. doi: 10.1016/j.jconrel.2006.04.015. [DOI] [PubMed] [Google Scholar]
- 101.Rivero RM, Ruiz JM, García PC, López-Lefebre LR, Sánchez E, Romero L. Resistance to cold and heat stress: accumulation of phenolics compounds in tomato and watermelon plants. Plant Sci. 2001;160:315–321. doi: 10.1016/s0168-9452(00)00395-2. [DOI] [PubMed] [Google Scholar]
- 102.Rupasinghe VHP, Clegg S. Total antioxidant capacity, total phenolics content, mineral elements and histamine concentration in wines of different fruit sources. J Food Compos Analy. 2007;20:133–7. [Google Scholar]
- 103.Saftner R, Luo Y, McEvoy J, Abbott JA, Vinyard B. Quality characteristics of fresh-cut watermelon slices from non-treated and 1-methylcyclopropene-and/or ethylene-treated whole fruit. Postharvest Biol Technol. 2007;44:71–79. [Google Scholar]
- 104.Salman H, Bergman M, Djaldetti M, Bessler H. Lycopene affects proliferation and apoptosis of four malignant cell lines. Biomed Pharmacother. 2007;61:366–369. doi: 10.1016/j.biopha.2007.02.015. [DOI] [PubMed] [Google Scholar]
- 105.Scolastici C, Alves de Lima RO, Barbisan LF, Ferreira ALA, Ribeiro DA, Salvadori DMF. Antigenotoxicity and antimutagenicity of lycopene in HepG2 cell line evaluated by the comet assay and micronucleus test. Toxicol In Vitro. 2008;22:510–514. doi: 10.1016/j.tiv.2007.11.002. [DOI] [PubMed] [Google Scholar]
- 106.Sesso HD, Buring JE, Norkus P, Gaziano JM. Plasma lycopene, other carotenoids and retinal and risk of cardiovascular diseases in men. Am J Clin Nutr. 2005;79:47–53. doi: 10.1093/ajcn/79.1.47. [DOI] [PubMed] [Google Scholar]
- 107.Shi J, Maguer ML. Lycopene in tomatoes: chemical and physical properties affected by food processing. Crit Rev Food Sci Nutr. 2000;40:1–42. doi: 10.1080/10408690091189275. [DOI] [PubMed] [Google Scholar]
- 108.Slattery ML, Benson J, Curtin K, Ma KN, Schaeffer D, Potter JD. Carotenoids and colon cancer. Am J Clin Nutr. 2000;71:575–582. doi: 10.1093/ajcn/71.2.575. [DOI] [PubMed] [Google Scholar]
- 109.Stefani ED, Oreggia F, Boffeta P, Deneo-Pellegrini H, Ronco A, Mendilaharsu M. Tomatoes, tomato-rich foods, lycopene and cancer of the upper aerodigestive tract: a case control in Uruguay. Oral Oncol. 2000;36:47–53. doi: 10.1016/s1368-8375(99)00050-0. [DOI] [PubMed] [Google Scholar]
- 110.Sugiura M, Nakamura M, Ikoma Y, Yano M, Ogawa K, Matsumoto H, et al. Serum carotenoid concentrations are inversely associated with serum aminotransferases in hyperglycemic subjects. Diabetes Res Clin Pract. 2006;71:82–91. doi: 10.1016/j.diabres.2005.05.004. [DOI] [PubMed] [Google Scholar]
- 111.Tadmor Y, King S, Levi A, Davis A, Meir A, Wasserman B, et al. Comparative fruit colouration in watermelon and tomato. Food Res Int. 2005;38:837–841. [Google Scholar]
- 112.Tang FY, Cho HJ, Pai MH, Chen YH. Concomitant supplementation of lycopene and eicosapentaenoic acid inhibits the proliferation of human colon cancer cells. J Nutr Biochem. 2009;20:426–434. doi: 10.1016/j.jnutbio.2008.05.001. [DOI] [PubMed] [Google Scholar]
- 113.Upritchard JE, Sutherland WH, Mann JI. Effect of supplementation with tomato juice, vitamin E, and vitamin C on LDL oxidation and products of inflammatory activity in type 2 diabetes. Diabetes Care. 2000;23:733–738. doi: 10.2337/diacare.23.6.733. [DOI] [PubMed] [Google Scholar]
- 114.Verschuren L, Wielinga PY, van Duyvenvoorde W, Tijani S, Toet K, van Ommen B, et al. A dietary mixture containing fish oil, resveratrol, lycopene, catechins, and vitamins E and C reduces atherosclerosis in transgenic mice. J Nutr. 2011;141:863–869. doi: 10.3945/jn.110.133751. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 115.Wang L, Liu S, Manson JE, Gaziano JM, Buring JE, Sesso HD. The consumption of lycopene and tomato-based food products is not associated with the risk of type 2 diabetes in women. J Nutr. 2006;136:620–625. doi: 10.1093/jn/136.3.620. [DOI] [PubMed] [Google Scholar]
- 116.Weisburger JH. Lycopene and tomato products in health promotion. Exp Biol Med. 2002;227:924–927. doi: 10.1177/153537020222701014. [DOI] [PubMed] [Google Scholar]
- 117.Wu G, Collins JK, Perkins-Veazie P, Siddiq M, Dolan KD, Kelly KA, et al. Dietary supplementation with watermelon pomace juice enhances arginine availability and ameliorates the metabolic syndrome in Zucker diabetic fatty rats. J Nutr. 2007;137:2680–2685. doi: 10.1093/jn/137.12.2680. [DOI] [PubMed] [Google Scholar]
- 118.Zhang D, Hamauzu Y. Phenolic compounds and their antioxidant properties in different tissues of carrots (Daucus carota L.) J Food Agric Environ. 2004;2:95–100. [Google Scholar]
- 119.Zohary, D, Hopf M, Weiss E. Domestication of plants in the old world: The origin and spread of domesticated plants in Southwest Asia, Europe, and the Mediterranean Basin. 4th ed. Oxford: Oxford Univ. Press; 2012. [Google Scholar]