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African Journal of Traditional, Complementary, and Alternative Medicines logoLink to African Journal of Traditional, Complementary, and Alternative Medicines
. 2009 Dec 30;7(2):109–112. doi: 10.4314/ajtcam.v7i2.50864

Effect of Cuscuta Reflexa Stem and Calotropis Procera Leaf Extracts on Glucose Tolerance in Glucose-Induced Hyperglycemic Rats and Mice

Mohammed Rahmatullah 1,, Shamsuddin Sultan 2, Tanzila Taher Toma 1, Sayeda-a-Safa Lucky 1, Majeedul H Chowdhury 2, Wahid Mozammel Haque 1, Eashmat Ara Annay 1, Rownak Jahan 1
PMCID: PMC3021163  PMID: 21304621

Abstract

Cuscuta reflexa (whole plant) and Calotropis procera (leaves) are used in folk medicine of Bangladesh to control blood sugar in patients suffering from diabetes mellitus. The hypoglycemic effects of methanol and chloroform extracts of whole plants of Cuscuta reflexa, and methanol extract of leaves of Calotropis procera were investigated in oral glucose tolerance tests in Long Evans rats and Swiss albino mice, respectively. Both methanol and chloroform extracts of Cuscuta reflexa whole plant demonstrated significant oral hypoglycemic activity in glucose-loaded rats at doses of 50, 100 and 200 mg/kg body weight. The methanol extract of leaves of Calotropis procera, when tested at doses of 100 and 250 mg/kg body weight did not demonstrate any oral hypoglycemic effect when tested in glucose-loaded mice.

Keywords: Cuscuta reflexa, Calotropis procera, hypoglycemic activity, oral glucose tolerance test

Introduction

Cuscuta reflexa Roxb. (family: Cuscutaceae alternate Covolvulaceae, nature: a parasitic vine) is prevalent in various regions of Bangladesh. Cuscuta reflexa is known to contain a number of α-glucosidase inhibitory compounds (Anis et al., 2002). A new flavanone- reflexin (Tripathi et al., 2005), tetrahydrofuran derivatives and a coumarin (Uddin et al., 2007) have been isolated from stems of the plant. Methanol extracts of the stem reportedly demonstrated anti-steroidogenic (Gupta et al., 2003), and antibacterial activities (Pal et al., 2006).

The various pharmacological activities of whole plant or plant parts including latex of Calotropis procera (Ait.) R. Brown (family: Asclepiadaceae, nature: shrub, synonym: Calotropis gigantea) have been documented. Reported activities included analgesic and anthelmintic activities in the flowers (Pathak and Argal, 2007; Iqbal et al., 2005), antipyretic activity in the roots (Chitme et al., 2005), antinociceptive activity in latex (Soares et al., 2005), anti-diarrheal activity in aerial parts (Chitme et al., 2004), anti-fertility activity in the roots (Kamath and Rana, 2002), neuromuscular blocking activity in aerial parts (Mossa et al., 1991), and hepatoprotective activity in stems (Lodhi et al., 2009). The latex of the plant, in addition, reportedly demonstrated antioxidant and protective effect against alloxan-induced diabetes in rats (Roy et al., 2005).

Diabetes mellitus (especially Type 2 diabetes) is a disease which affects a considerable section (more than 4%) of the rural population of Bangladesh (Sayeed et al., 2003). Traditional or folk medicinal practitioners, who form the primary healthcare providers to most of the rural population, use a variety of medicinal plants or plant parts to treat this disease. Two of the widely used plants for treatment of this disease are the stems (vines) of Cuscuta reflexa and leaves of Calotropis procera. It was the objective of the present study to evaluate the hypoglycemic potential of methanol and chloroform extracts of stems of Cuscuta reflexa and methanol extract of leaves of Calotropis procera.

Materials and Methods

Preparation of extracts

Five hundred g of air-dried powdered stems (Cuscuta reflexa) or leaves (Calotropis procera) were extracted by maceration with 4 volumes (w/v) of methanol (MeOH) or chloroform until exhaustion. The extracts were freed from solvent using a vacuum rotary evaporator at 50°C. The residues were stored at 4°C in a refrigerator till use. Immediately prior to using, extracts were suspended thoroughly in distilled water containing 1% Tween-80. Following collection and prior to extraction, specimens of both plants were authenticated at the Bangladesh National Herbarium.

Animals

Long Evans rats (weighing 90–120 g) and Swiss albino mice (weighing 15–25 g) were obtained from the animal house, International Cenre for Diarrheal Disease Research, Bangladesh (ICDDR, B). Rats and mice were housed in proper cages with adequate lighting and ventilation with an ambient temperature of 23–26°C. All experimental studies were conducted following the ethical guidelines of the National Institute of Health, USA and appropriate permissions obtained from the relevant authorities of the University of Development Alternative prior to commencing the experiments.

Studied activity

Oral glucose tolerance tests were conducted with slight modifications of method as described earlier (Joy and Kuttan, 1999). Two separate experiments were conducted, one for the testing of hypoglycemic activity present in methanol and chloroform extracts of Cuscuta reflexa stems, and the second for testing any hypoglycemic activity present in methanol extract of Calotropis procera leaves. For testing of Cuscuta reflexa stem methanol and chloroform extracts, 16 hr-fasted rats were divided into eight groups of five rats each. Group 1 served as control and received distilled water (containing 1% Tween-80). Group 2 received a standard drug glibenclamide at a dose of 10 mg/kg body weight (bw). Groups 3–5 received Cuscuta reflexa stem methanol extract at doses of 50, 100 and 200 mg/kg bw, respectively. Groups 6–8 received Cuscuta reflexa stem chloroform extract at doses of 50, 100 and 200 mg/kg bw, respectively. For testing of Calotropis procera leaf methanol extract, 16 hr-fasted mice were divided into four groups of six mice each. Group 1 received distilled water and group 2 received glibenclamide at a dose of 10 mg/kg bw. Groups 3 and 4 received methanol extract at doses of 100 and 250 mg/kg bw, respectively. All administrations were done by gavage. After 60 mins of extract administration, rats or mice of all groups were orally treated with 2 g/kg bw of glucose. Following another 120 mins after glucose loading, animals were sacrificed and serum collected. Serum glucose levels were measured immediately by glucose oxidase method (Trinder, 1969).

Statistical analysis

The results were expressed as means ± S.E.M, and analyzed for statistical significance using Student's t-test. P values< 0.05 were considered significant.

Results

Cuscuta reflexa stem methanol and chloroform extracts

The methanol extract of Cuscuta reflexa stems caused a statistically significant and dose-dependent reduction in serum glucose levels in oral glucose-challenged rats, when compared to control group (Group 1). However, even at the highest dose tested (500 mg extract/kg bw), serum glucose levels were higher than that obtained with the standard drug glibenclamide (Table 1). Nevertheless, the results are promising enough to conduct further studies on isolation of active principle(s) from the extract that is responsible for the hypoglycemic effect. On, the other hand, the chloroform extract, although it demonstrated statistically significant reductions in serum glucose levels, did not show any dose-dependency. However, even at the lowest dose administered (100 mg extract/kg bw), serum glucose levels were lower in glucose-challenged rats than obtained with a comparable dose of methanol extract. Thus both extracts showed promise in their hypoglycemic potential.

Table 1.

Effect of oral administration of Cuscuta reflexa stem methanol and chloroform extracts or Calotropis procera leaf methanol extract on oral glucose tolerance in rats and micea

Group Serum glucose (mg/dL)
Cuscuta reflexa Calotropis procera
1 87.0 ± 3.8 114.2 ± 11.7
2 37.8 ± 4.1* 57.5 ± 7.3**
3 74.6 ± 3.3*** 132.9 ± 13.3
4 71.5 ± 4.0** 95.0 ± 17.1
5 69.1 ± 3.9** -
6 54.1 ± 2.8* -
7 60.0 ± 6.8** -
8 58.9 ± 4.0* -
a

Values are means ± S.E.M.; *P<0.001, **P<0.01, ***P<0.05 vs. Group 1.

Calotropis procera leaf methanol extract

In contrast to the results obtained with Cuscuta reflexa, methanol extract of Calotropis procera did not demonstrate any significant lowering of serum glucose levels at both experimental doses than the control group (Group 1) in mice (Table 1). However, serum glucose levels fell from 132.9 ± 13.3 mg/dL (at a dose of 100 mg extract/kg bw) to 95.0 ± 17.1 mg/dL (at a dose of 250 mg/kg bw). It is to be noted that at the latter dose, the serum glucose levels were lesser than the control group (114.2 ± 11.7 mg/dL), even though this result was not statistically significant from the control. Any higher doses were not tried, as all experimental doses were administered based on amounts administered to human patients by traditional medicinal practitioners.

Discussion

Cuscuta reflexa contains a number of compounds like flavonoids (kaempferol, quercitin), coumarins, and flavonoid glycosides (Ghani, 2003). Earlier studies have shown that both kaempferol and quercetin could significantly improve insulin-stimulated glucose uptake in mature 3T3-L1 adipocytes. It was further reported that these two compounds act at multiple targets to ameliorate hyperglycemia (Fang et al., 2008). Aqueous and butanolic extracts of aerial parts of Equisetum myriochaetum containing kaempferol glucosides demonstrated hypoglycemic effects in streptozotocin-induced diabetic rats (Andrade Cetto et al., 2000). Quercetin 3-O-β-galacturonopyranoside and quercetin 7-O-β-glucopyranoside, isolated from aerial parts of Cynanchum acutum reportedly exhibited significant antioxidant and antidiabetic activities (Fawzy et al., 2008).

It has been reported earlier that the latex of Calotropis procera demonstrated antioxidant and anti-hyperglycemic effects against alloxan-induced diabetes in rats (Roy et al., 2005). Our experimental results with the methanol extract of leaves of this plant did not show any significant hypoglycemic activity. This can stem from two factors. First, leaves, instead of latex was used in the present experiment. Second, in the earlier reported results, latex was fed for days to observe the anti-hyperglycemic effect. In the present study, leaf extract was administered only 60 mins prior to glucose loading. An additional factor may be that the doses used in the present study were not large enough to observe significant hypoglycemic effects. It may be noted that a dose-dependent reduction of serum glucose was observed and at the highest dose tested, serum glucose in experimental mice was less than that in the control group.

Taken together, our results in combination with previously published reports justify the use of Cuscuta reflexa by traditional medicinal practitioners of Bangladesh to treat diabetes, and suggest that administration of leaves of Calotropis procera might also serve as an effective way to bring blood sugar in diabetic patients under control, when given in high doses.

Acknowledgements

This work was funded by the University of Development Alternative.

References

  • 1.Andrade Cetto A, Wiedenfeld H, Revilla MC, Sergio IA. Hypoglycemic effect of Equisetum myriochaetum aerial parts on streptozotocin diabetic rats. J Ethnopharmacol. 2000;72:129–133. doi: 10.1016/s0378-8741(00)00218-x. [DOI] [PubMed] [Google Scholar]
  • 2.Anis E, Anis I, Ahmed S, Mustafa G, Malik A, Afza N, Hai SM, Shahzad-ul-hussan S, Choudhary MI. α-glucosidase inhibitory constituents from Cuscuta reflexa. Chem Pharm Bull (Tokyo) 2002;50:112–114. doi: 10.1248/cpb.50.112. [DOI] [PubMed] [Google Scholar]
  • 3.Chitme HR, Chandra M, Kaushik S. Studies on anti-diarrhoeal activity of Calotropis gigantea R.Br. in experimental animals. J Pharm Pharm Sci. 2004;7:70–75. [PubMed] [Google Scholar]
  • 4.Chitme HR, Chandra R, Kaushik S. Evaluation of antipyretic activity of Calotropis gigantea (Asclepiadaceae) in experimental animals. Phytother Res. 2005;19:454–456. doi: 10.1002/ptr.1672. [DOI] [PubMed] [Google Scholar]
  • 5.Fang XK, Gao J, Zhu DN. Kaempferol and quercetin isolated from Euonymus alatus improve glucose uptake of 3T3-L1 cells without adipogenesis activity. Life Sci. 2008;82:615–622. doi: 10.1016/j.lfs.2007.12.021. [DOI] [PubMed] [Google Scholar]
  • 6.Fawzy GA, Abdallah HM, Marzouk MS, Soliman FM, Sleem AA. Antidiabetic and antioxidant activities of major flavonoids of Cynanchum acutum L. (Asclepiadaceae) growing in Egypt. Z Naturforsch [c] 2008;63:658–662. doi: 10.1515/znc-2008-9-1008. [DOI] [PubMed] [Google Scholar]
  • 7.Ghani A. Medicinal Plants of Bangladesh. 2nd Edn. Asiatic Society of Bangladesh; 2003. p. 198. [Google Scholar]
  • 8.Gupta M, Mazumder UK, Pal DK, Bhattacharya S. Anti-steroidogenic activity of methanolic extract of Cuscuta reflexa Roxb. stem and Corchorus olitorius Linn. seed in mouse ovary. Indian J Exp Biol. 2003;41:641–644. [PubMed] [Google Scholar]
  • 9.Iqbal Z, Lateef M, Jabbar A, Muhammad G, Khan MN. Anthelmintic activity of Calotropis procera (Ait.) Ait. F. flowers in sheep. J Ethnopharmacol. 2005;102:256–261. doi: 10.1016/j.jep.2005.06.022. [DOI] [PubMed] [Google Scholar]
  • 10.Joy KL, Kuttan R. Anti-diabetic activity of Picrorrhiza kurroa extract. J Ethnopharmacol. 1999;167:143–148. doi: 10.1016/s0378-8741(98)00243-8. [DOI] [PubMed] [Google Scholar]
  • 11.Kamath JV, Rana AC. Preliminary study on antifertility activity of Calotropis procera roots in female rats. Fitoterapia. 2002;73:111–115. doi: 10.1016/s0367-326x(02)00005-9. [DOI] [PubMed] [Google Scholar]
  • 12.Lodhi G, Singh HK, Pant KK, Hussain Z. Hepatoprotective effects of Calotropis gigantea extract against carbon tetrachloride induced liver injury in rats. Acta Pharm. 2009;59:89–96. doi: 10.2478/v10007-009-0002-2. [DOI] [PubMed] [Google Scholar]
  • 13.Mossa JS, Tariq M, Mohsin A, Ageel AM, al-Yahya MA, al-Said MS, Rafatullah S. Pharmacological studies on aerial parts of Calotropis procera. Am J Chin Med. 1991;19:223–231. doi: 10.1142/S0192415X91000302. [DOI] [PubMed] [Google Scholar]
  • 14.Pal DK, Mandal M, Senthilkumar GP, Padhiari A. Antibacterial activity of Cuscuta reflexa stem and Corchorus olitorius seed. Fitoterapia. 2006;77:589–591. doi: 10.1016/j.fitote.2006.06.015. [DOI] [PubMed] [Google Scholar]
  • 15.Pathak AK, Argal A. Analgesic activity of Calotropis gigantea flower. Fitoterapia. 2007;78:40–42. doi: 10.1016/j.fitote.2006.09.023. [DOI] [PubMed] [Google Scholar]
  • 16.Roy S, Sehgal R, Padhy BM, Kumar VL. Antioxidant and protective effect of latex of Calotropis procera against alloxan-induced diabetes in rats. J Ethnopharmacol. 2005;102:470–473. doi: 10.1016/j.jep.2005.06.026. [DOI] [PubMed] [Google Scholar]
  • 17.Sayeed MA, Mahtab H, Khanam PA, Latif ZA, Ali SMK, Banu A, Ahren B, Khan AKA. Diabetes and impaired fasting glycemia in a rural population of Bangladesh. Diabetes care. 2003;26:1034–1039. doi: 10.2337/diacare.26.4.1034. [DOI] [PubMed] [Google Scholar]
  • 18.Soares PM, Lima SR, Matos SG, Andrade MM, Patrocínio MC, de Freitas CD, Ramos MV, Criddle DN, Cardi BA, Carvalho KM, Assreuy AM, Vasconcelos SM. Antinociceptive activity of Calotropis procera latex in mice. J Ethnopharmacol. 2005;99:125–129. doi: 10.1016/j.jep.2005.02.010. [DOI] [PubMed] [Google Scholar]
  • 19.Trinder P. Determination of glucose using glucose oxidase with an alternative oxygen acceptor. Annals Clin Biochem. 1969;6:24–27. [Google Scholar]
  • 20.Tripathi VJ, Yadav SB, Upadhyay AK. A new flavanone, reflexin, from Cuscuta reflexa and its selective sensing of nitric oxide. Appl Biochem Biotechnol. 2005;127:63–67. doi: 10.1385/abab:127:1:063. [DOI] [PubMed] [Google Scholar]
  • 21.Uddin SJ, Shilpi JA, Middleton M, Byres M, Shoeb M, Nahar L, Sarker SD. Swarnalin and cis-swarnalin, two new tetrahydrofuran derivatives with free radical scavenging activity, from the aerial parts of Cuscuta reflexa. Nat Prod Res. 2007;21:663–668. doi: 10.1080/14786410701371405. [DOI] [PubMed] [Google Scholar]

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