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. 2023 Nov 17;2023:3105251. doi: 10.1155/2023/3105251

Herbal and Natural Treatments for the Management of the Glaucoma: An Update

Livio Vitiello 1,, Luigi Capasso 2, Giovanni Cembalo 3, Ilaria De Pascale 4, Roberto Imparato 5, Maddalena De Bernardo 3
PMCID: PMC10673672  PMID: 38027044

Abstract

Glaucoma causes the degeneration of the retinal ganglion cells (RGCs) and their axons, inducing a tissue reshaping that affects both the retina and the optic nerve head. Glaucoma care especially focuses on reducing intraocular pressure, a significant risk factor for progressive damage to the optic nerve. The use of natural treatments, such as herbs, vitamins, and minerals, is becoming increasingly popular today. While plants are a rich source of novel biologically active compounds, only a small percentage of them have been phytochemically examined and evaluated for their medicinal potential. It is necessary for eye care professionals to inform their glaucoma patients about the therapy, protection, and efficacy of commonly used herbal medicines, considering the widespread use of herbal medicines. The purpose of this review is to examine evidence related to the most widely used herbal medicines for the management and treatment of glaucoma, to better understand the potential benefits of these natural compounds as supplementary therapy.

1. Introduction

Glaucoma is the leading cause of irreversible blindness worldwide [1]. The disease has a complex etiology and a wide range of risk factors; all these factors can be associated with death of retinal ganglion cells (RGCs) and to tissue remodelling affecting both the retina and the optic nerve head. Furthermore, the optic nerve becomes thinner, and the lateral geniculate ganglion cells partly vanish over time. Moreover, the blood flow tends to be reduced in different ocular tissues in glaucoma patients, thus contributing to neuronal damage [2]. Reducing intraocular pressure (IOP), a substantial risk factor for progressive optic nerve injury, is a major focus of glaucoma treatment. Nevertheless, it is obvious that IOP is only one of several variables that lead to glaucoma pathophysiology [3].

Neuroprotection is a fast-growing area of investigation. This topic is really challenging because it is a new treatment option for frustrating disorders that may worsen despite optimal therapy, as in the case of glaucoma [1]. One of the first medicinal plants used for glaucoma was pilocarpine, a parasympathomimetic alkaloid extracted from a South American shrub, Pilocarpus microphyllus [4].

Considering the extensive usage of herbal medications, eye care professionals should educate their glaucoma patients about the treatment, safety, and efficacy of these drugs. In fact, nowadays, using natural remedies like herbs, vitamins, and minerals to treat ocular disorders is becoming more and more popular [510]. Alternative medications have a $109 billion global market and are commonly used by up to 52 percent of the general population [11, 12]. Despite being a plentiful source of new biologically active compounds, only very few plants have been phytochemically analyzed and evaluated for their potential as medicines [13, 14].

Today, while active compounds continue to be extracted from medicinal plants by the pharmaceutical industry, standardized techniques are used to achieve this aim. In fact, in the United States, the Food and Drug Administration (FDA) enforces these uniform procedures and controls prescription medications, but not complementary medicines, such as herbal medicines and dietary supplements [10]. Considering that glaucoma induces a RGC degeneration, the neuroprotection has gained progressively more interest as a new strategy to prevent or delay the progression of the morphological and functional glaucomatous damages. Since the use of natural treatments to treat several pathologies is becoming more popular, claiming for efficacy and reduced adverse events, it could be interesting to deeply examine the possible use of herbal medicines applied to the glaucoma management.

For this reason, the purpose of this review is to assess evidence related to the most widely used herbal medicines in the management and treatment of glaucoma through an overview of the scientifically published literature and to better understand the potential benefits of these natural compounds as supplementary therapy for glaucoma.

2. Materials and Methods

We carried out a search on the PubMed and Scopus medical databases. To gain a broader perspective and comprehension of the problem, a preliminary generic Google search was also performed. The database search strategy was formulated around the term “glaucoma” and several other terms regarding medicinal herbs, natural compounds, and phytotherapy (“Baicalein”, “Baicalin”, “Wogonin”, “Ashawagandha”, “Withania”, “phytotherapy” “Saffron”, “Crocus sativus”, “Bilberry”, “Anthocyanin”, “Erigeron”, “Curcuma”, “Curcumin”, “Ginkgo Biloba”, “Salvia miltiorrhiza”). The search terms were selected after considering the available literature and/or gathered from linked bibliographies. Only full articles and case reports were reviewed. Duplicate and unrelated papers were excluded. Bibliographies from the initial searches were also manually searched for additional inclusions.

3. Results

3.1. Ginkgo biloba

The history of Ginkgo biloba began around 250 million years ago, and it is a member of the earliest order of true trees. These trees are commonly planted in Asian countries, especially in China and Japan, and the seeds are used to treat a wide range of systemic disorders [15, 16]. Among its properties, vasoactive effects [17, 18], hemorheological regulation [19, 20], anti-inflammatory [2123], and antioxidative capacities [24] have been demonstrated. The extract from Ginkgo biloba leaves, known as Ginkgo biloba extract 761 (EGb761), has been demonstrated to be helpful for dementia and cognitive impairment in modern medicine [25]. Researchers have examined Ginkgo biloba for glaucoma due to the molecular and mechanical parallels between Alzheimer's disease and glaucoma [26]. The significance of mitochondrial dysfunction in the glaucoma etiology has been shown in a number of investigations [27]. Only antioxidants with mitochondrial penetration potential can serve as effective neuroprotective agents, and some compounds in Ginkgo, such as polyphenolic flavonoids, may theoretically reduce oxidative stress in the mitochondria and shield RGCs [16, 28, 29].

Recently, one in vitro study revealed a significative reduction of damages induced by hydrogen peroxide on RGCs as well as in an animal model [30]. In another in vivo study, the effects of Ginkgo biloba extract (GBE) on elevated IOP and RGC density were evaluated, revealing that both pretreatment and early posttreatment with EGb761 have a successful neuroprotective effect in a rat model of chronic glaucoma [31].

The therapy with GBE in a group of patients with normal tension glaucoma (NTG) seems not to have any impact on the mean defect or contrast sensitivity on the 24-2 SITA standard visual field [26]. In this study, patients who had just received an NTG diagnosis had two 4-week treatment phases, each followed by an 8-week washout period, showing no significant improvement in the management of the disease [32].

Conversely, in another retrospective study, forty-two eyes of 42 patients with treated NTG were assessed. They received 80 mg GBE twice daily, and they had at least 5 visual field tests using the Humphrey Visual Field Analyzer for more than a 4-year period before and after GBE treatment. Indexes such as mean deviation, pattern standard deviation, and visual field index were measured, showing that GBE administration slowed the progression of visual field damage in NTG patients [33].

For this reason, considering the controversial results emerging from studies in the literature, more studies are needed to establish the actual usefulness of GBE in glaucoma therapy and management. Furthermore, it is crucial to consider that none of the studies currently published in the literature on Ginkgo biloba deals with the treatment and management of primary open-angle glaucoma (POAG), which accounts for nearly 90% of glaucoma cases.

3.2. Scutellaria baicalensis Georgi Derivates

Scutellaria baicalensis Georgi is a medicinal herb widely available in several East Asian countries and in China. Since ancient times, its dried root, known as Scutellariae radix, has been used in the therapeutic treatment of several illnesses, including hepatitis, hepatoma, leukemia, and hyperlipidemia. Additionally, this medicinal plant can reduce blood pressure, capillary permeability, and serum cholesterol levels [3436].

Baicalin (5,6-dihydroxy-7-O-glucuronide), wogonin (5,7-dihydroxy-8-methoxyflavone), and baicalein (5,6,7-trihydroxyflavone) are the principal bioflavones extracted from this radix. They have a broad spectrum of bioactivity, including antioxidant, anticancer, anti-inflammation effects, and neuroprotection [3742]. These bioflavones have been demonstrated to exert their effects through different pathways, such as inhibiting nitric oxide production in macrophages and the gene expression of lipopolysaccharide inducible nitric oxide synthase, suppressing cyclooxygenases-2 gene expression and prostaglandin E2 production, and downregulating different proinflammatory mediators and cytokines [4347]. Particularly, they are capable of reducing interleukin-8 (IL-8), which is generally increased in POAG patients [48].

Concerning their antioxidant activities, it has been proved that these compounds are able to scavenge reactive oxygen species and to prevent their production by inhibiting xanthine oxidase [49, 50]. Moreover, they can act as iron chelators and inhibitors of the Fenton reaction [51].

The neuroprotective effects against oxidative stress of both baicalin and baicalein have been proved in RGCs. An in vitro study carried out in an immortalized RGC line (RGC-5) demonstrated that baicalein effectively rescued RGCs in three different oxidative stress models [52]. Equally, in the RGC-5, baicalin showed effective, dose-dependent protective effects against several different oxidative insults, such as serum deprivation, hydrogen peroxide treatment, and light exposure [53]. Therefore, these results suggest that baicalin and baicalein have a strong capacity to protect RGCs from oxidative stress, assuming their possible function in reducing RGC loss in glaucoma.

In addition, an in vitro study by Gong and Zhu on human trabecular meshwork cells [54] showed how baicalin was able to reduce intracellular reactive oxygen species and increase cell survival, inhibiting the proinflammatory factor interleukin-1α (IL-1α) and endothelial leucocyte adhesion molecule-1 (ELAM-1) production, decreasing activities of senescence-associated beta-galactosidase (SA-β-gal), and lowering levels of carbonylated protein.

For flavonoid-induced protection against oxidative stress in brain cells, three separate pathways have been identified: raising glutathione levels, removing reactive oxygen species, and blocking Ca2+ influx [55].

Regarding the role of wogonin in preventing RGC loss in glaucoma, a study by Xu et al. [56] on the optic nerve crush model proved its ability to suppress inflammatory responses and rescue RGC death. In fact, wogonin can reduce RGC loss and inhibit RGC apoptosis, decreasing the level of toll-like receptor 4 (TLR4 expression), nuclear factor kappa-light-chain-enhancer of activated B cells-P65 (NF-κB-P65), and NF-κB-P65 phosphorylation. For this reason, all these bioflavones could be considered possible therapeutic agents for the glaucoma treatment and management.

Finally, although the bioflavones extracted from the Scutellaria baicalensis Georgi have proven their ability in preventing RGC loss in glaucomatous animal models in vitro, they have not been used yet in vivo glaucoma patients, and, consequently, their efficacy in the glaucoma management in human subjects needs to be further demonstrated.

3.3. Crocus sativus L. (Saffron)

The dried stigmas of the stemless plant Crocus sativus L. flower compose the saffron, which is mostly used in cooking as a flavouring and colouring spice. Picrocrocin, safranal, crocetin, and crocin are the pharmacologically active components of saffron [57, 58].

Saffron or its active ingredients may possibly have neuroprotective, antioxidant, anti-inflammatory, antidepressive, anxiolytic, anticonvulsant, antiatherogenic, hypolipidemic, antihypertensive, and even antitumor actions, according to growing data from pharmacological research [5961].

Crocin and crocetin were found to be able to inhibit RGC death in mouse and rat models of ischemia/reperfusion [6264].

The decrease in the number of positive terminal deoxynucleotidyl transferase dUTP nick end labelling (TUNEL) cells and 8-hydroxy-2-deoxyguanosine positive cells, as well as the elevated phosphorylation levels of c-Jun, c-Jun N-terminal kinases (JNK), p38, and NF-B following retinal damage, are all examples of mechanisms that may be responsible for the potential neuroprotective effects against ischemic damage [62].

Recently, in a mouse model of glaucoma, the neuroprotective and anti-inflammatory effects of the saffron extract have been confirmed [65]. In fact, in both the ocular hypertension (OHT) eye and the normotensive fellow eye, saffron extract therapy decreased the number of microglial cells and the symptoms of microglial activation. Additionally, supplementing with saffron extract partially corrected the downregulation of Purinergic Receptor P2RY12 brought on by the IOP increase [65]. Immediately after the injury, P2RY12 expression is upregulated. On the other hand, a few hours later, P2RY12 expression is downregulated and disappears in highly active microglial cells [66]. As a result, this finding suggests that saffron extract may reduce inflammation by controlling P2RY12 expression [65]. Finally, in this model, it has also been shown that saffron may stop OHT eyes from losing considerable amounts of transcription factor Brn3a+ RGCs [65]. The antioxidant and anti-inflammatory properties of the saffron extract could be responsible for this substance's neuroprotective benefits [65].

The few clinical investigations that have been conducted on individuals with POAG have examined any potential ocular hypotensive effects, and their findings have been conflicting. Saffron supplementation (1 g twice a week) in a randomized controlled pilot study did not seem to have an impact on IOP in the near term (1 month) [67]. However, according to a different pilot study carried out on 34 clinically stable POAG patients, oral saffron supplementation (30 mg daily for one month) can considerably lower IOP after three weeks. Though, this effect is reversed after a four-week washout period [68].

3.4. Coleus forskohlii

The plant Coleus forskohlii has been used in Ayurvedic and Hindu traditional medicine for a very long time. Its root, which has historically been used in medicine, includes forskolin, the active constituent.

Through the activation of the enzyme adenylate cyclase, forskolin's main mechanism of action is to enhance cyclic adenosine monophosphate (cAMP) and cAMP-mediated activities [69].

Forskolin is able to inhibit basophil and mast cell degranulation and histamine release [70], lower blood pressure [71] and IOP [72], inhibit platelet aggregation [73], and promote vasodilation [74], bronchodilation [75], and thyroid hormone secretion [76], as well as stimulate lipolysis in fat cells [77].

Forskolin also has the ability to block the binding of platelet-activating factor (PAF), irrespective of its ability to stimulate cAMP production. Additionally, forskolin can reduce glucose transfer in erythrocytes, adipocytes, platelets, and other cells [78]. It also appears to have an impact on different membrane transport proteins [78].

Several studies using topical forskolin applications to decrease IOP have been carried out, with contrasting results.

IOP was significantly reduced in a dose-dependent manner in the eyes of normal rabbits using solutions of 2%, 1%, and 0.5% forskolin. These effects peaked in 2-3 hours and lasted up to 10 hours [79]. On the other hand, glaucomatous monkeys treated for two days with a 1% forskolin solution failed to appreciably lower IOP [80]. However, Caprioli and Sears found that giving rabbits, monkeys, and people a topical 1% forskolin solution significantly reduced their IOP. This effect started at one hour after application and persisted for at least five hours [81]. Forskolin has also been demonstrated to be beneficial at lowering IOP and reducing aqueous outflow in human trials with only healthy volunteers.

In a randomized, crossover experiment, Meyer et al. evaluated the effects of 1% forskolin against placebo on 10 healthy volunteers. IOP decreased in the first trial in both the forskolin and placebo groups, which was attributable to the local anesthetic oxybuprocaine. In the second experiment, forskolin substantially reduced IOP compared to placebo when proxymetacaine was employed as the topical anesthetic [82]. Conversely, one dosage of a 1% forskolin solution had no impact in a different trial on 20 healthy participants, but two instillations spaced out by five minutes significantly reduced IOP and aqueous flow rate [83].

However, a research by Brubaker et al. found no evidence that forskolin could significantly reduce flow rate in a group of 15 healthy volunteers who received one dosage of 1% forskolin in each of three circumstances: during the day, while sleeping at night, and after receiving timolol pretreatment [84].

Clinical research on the use of forskolin in glaucoma patients is scarce, despite its topical use in healthy humans and animals that seems promising. Mutolo et al. studied twenty-two POAG patients already under treatment with IOP-lowering medications to determine the effects of a food supplement containing forskolin; homotaurine; carnosine; folic acid; vitamins B1, B2, and B6; and magnesium over the course of a 12-month period. They found a further IOP decrease and a foveal sensitivity and pattern electroretinogram amplitude improvement in treated patients with this food supplement, also showing a short-term neuroactive effect [85].

Due to a lack of information on the potential effects of forskolin on glaucomatous patients, especially if orally administered, further studies on this important topic are needed.

3.5. Vaccinium myrtillus (Bilberry)

Anthocyanins derived from Vaccinium myrtillus or bilberry are increasingly being used in ophthalmology. In fact, vascular tissues and eyes are particularly responsive to flavonoid anthocyanosides [86]. Strong antioxidant properties [87]; decreased capillary permeability and fragility [88]; collagen fiber stabilization and collagen biosynthesis promotion [89]; prevention of the release and synthesis of proinflammatory compounds such as histamine, prostaglandins, and leukotrienes [90]; inhibition of platelet aggregation [91]; and blood glucose level decrease [92] are just a few of the anthocyanins' mechanisms of action. Although there have not been many studies on this challenging topic, anthocyanins have shown promising actions in the glaucoma treatment and management.

In a recent study on mice [93], anthocyanins in bilberry extract (100 mg/kg/day or 500 mg/kg/day) were administered orally, and the expression levels of various molecular chaperones and RGC survival were appraised. This study showed that oral bilberry extract administration could suppress RGC death and increase glucose-regulated protein 78 (Grp78) and Grp94 protein levels, an effect which may underlie the neuroprotective effect of bilberry extract after optic nerve damage.

Caselli [94] evaluated eight patients with glaucoma that received a single dose of 200 mg anthocyanosides from bilberry, with significant improvements at the electroretinography.

In another study [95], a retrospective analysis was carried out by a chart review of 332 NTG subjects (209 men and 123 women), who were treated with anthocyanins (n = 132), GBE (n = 103), or no medication (controls, n = 97). Before and after therapy, the Humphrey Visual Field (HVF) test, best-corrected visual acuity, IOP, blood pressure, and fasting blood glucose levels were measured. HVF mean deviation is improved following anthocyanin and GBE therapy, indicating that anthocyanins and GBE may be useful in enhancing visual function in some NTG subjects.

Finally, Gizzi et al. [96] assessed 88 patients affected by ocular hypertension who were monitored for 12 weeks in a supplement registry. The patients were divided into three study groups by the authors: the first group received latanoprost plus Mirtogenol® (80 mg of bilberry extract, Mirtoselect®, plus 40 mg of Pycnogenol®), the second group received latanoprost alone, and the third group received dorzolamide-timolol plus Mirtogenol®. IOP, retinal blood flow, Zinn-Haller circle perfusion, and oxidative stress were evaluated. According to the study, all treatment groups showed statistically significant improvements in retinal microcirculation and IOP throughout the course of the trial, with a little more pronounced effect in the first group. In addition, Mirtogenol® users exhibited better perfusional patterns than patients who just used latanoprost. Additionally, supplemented participants showed a decrease in oxidative stress. In order to achieve normal IOP and ophthalmic microcirculatory parameters, supplement with Mirtogenol® in addition to local ocular therapies might be considered both safe and helpful.

To further understand the possible significance of anthocyanins in the management and therapy of glaucoma, more studies should be carried out in the future.

3.6. Ribes nigrum L. (Black Currant Fruits)

As bilberry, black currant fruit is rich in anthocyanins and is commonly consumed worldwide too. Black currants contain only four different anthocyanins, a simpler composition than bilberries. We found some published papers about black currant anthocyanin intake related to glaucoma progression.

Ohguro et al. [97] performed a randomized, placebo-controlled, double-masked trial concerning oral black currant anthocyanins (BCACs) and POAG progression in 38 patients in treatment with antiglaucomatous drops. BCACs (50 mg/day, n = 19) or their placebos (n = 19) were orally administered once daily for a 24-month period. The authors found a statistically significant improvement in ocular blood flow and in the visual field in the BCAC-treated group (oral administration of 50 mg/day). Nevertheless, they did not find significant changes in other ocular parameters, as in IOP values, during the study period.

In a randomized, placebo-controlled, double-masked 24-month trial on POAG patients (n = 19), Yoshida et al. [98] found that, after BCAC intake (2 capsules, 50 mg/day), the serum endothelin-1 (ET-1) concentration in POAG patients was significantly increased to levels similar to those of healthy subjects (n = 20). On the other hand, ET-1 values for placebo-treated patients remained lower, similar to the baseline.

Once more, Ohguro et al. [99] carried out a placebo-controlled, double-masked, crossover study in 21 POAG patients (BCACs, n = 12; placebo, n = 9) treated with a single antiglaucomatous drug and 12 healthy subjects treated once daily with oral BCACs (50 mg). They found a statistically significant decline in mean IOP values (at 4 weeks, p = 0.039) not only in healthy participants but also in POAG patients using BCACs (p = 0.027) after a 24-month period.

All these results suggest that oral BCAC intake may induce an improvement in ocular blood flow and a decrease in IOP levels both in healthy and POAG patients already treated with antiglaucomatous drugs.

3.7. Erigeron breviscapus

Erigeron breviscapus is an herbal medicine spread in Yunnan Province, well known as a Chinese medicinal plant for heart disease. Several studies have shown that it can improve blood circulation and reduce thrombotic events [100, 101].

We found a published article which correlates this plant intake to improvement in IOP values. In fact, Zhong et al. [102] performed a randomized, double-blind, clinical trial on POAG patients, with visual field defects and with a postsurgical IOP of less than 18 mmHg (n = 40 eyes), administering orally Erigeron tablets and placebo tablets, 2 tabs three times in a day for 6 months. Erigeron-treated group showed a significant decrease in mean defect and a significant increase in mean sensitivity (p < 0.05) after 6 months, while the placebo group did not show any significant changes. These results could suggest that Erigeron breviscapus intake may have a stimulating effect in glaucoma patients with a controlled range IOP.

3.8. Salvia miltiorrhiza

Salvia miltiorrhiza is a traditional botanical Chinese medicine that, when administered intravenously, seems to improve microcirculation [103]. For this reason, this extract may have neuroprotective effects on the retina in progressive glaucoma.

In a study carried out by Zhu and Cai on 36 pigmented rabbits, this botanical compound was found to protect the optic nerve from the damage related to increased IOP [104].

In a different study using a rat glaucoma model, Zhu et al. [105] reported the outcomes from 20 male Sprague Dawley rats that had their aqueous outflow blocked by laser radiation, compared to 10 control rats. In the laser-induced glaucoma model, they discovered that Salvia miltiorrhiza extract was unable to stop the IOP rise, but the therapy reduced cell death as the glaucoma advanced, suggesting its neuroprotective properties against the disease [105].

In a human study [106], a 2 g/mL solution of Salvia miltiorrhiza alone or in combination with other Chinese herbs was administered daily through intramuscular injection to 121 individuals (153 eyes) affected by moderate or late-stage POAG and under antiglaucomatous therapy. After 30 days, 49.7% of the eyes' visual field and 43.8% of the eyes' visual acuity had both improved. The four herbal remedies did not differ significantly from one another, but there was a statistically significant improvement compared to the untreated eyes. Following the monthly treatment, 19 eyes were reassessed 7–30 months later, and the results showed that 73.7% of the eyes had maintained or improved their visual fields, assuming a potential long-term effect of this herbal remedy.

4. Discussion

Glaucoma is a particularly complex disease, for both diagnosis and management [107114].

Neuroprotective therapy is another innovative method for managing glaucoma, and its goal is to stop or delay RGC degeneration and death [8].

Traditional Chinese medicine, already for about 50 years, has always focused on the beneficial and healing effects of natural compounds for the treatment of various diseases [115118].

For this reason, in recent years, several natural compounds have been analyzed to better understand their potential beneficial effects in the treatment of ocular neurodegenerative diseases, such as glaucoma and age-related macular degeneration [510].

Possible neuroprotective substances found in nature, such the bilberry and GBE, have received growing attention for this therapeutic approach [8]. Many of these compounds have been shown to increase choroidal and retinal circulation and facilitate retinal recovery after ischemic insult in animals [10]. However, to demonstrate the usefulness of neuroprotective medicines against glaucoma, including medicinal herbs, high-quality data is currently missing.

Concerning GBE, it has been shown that it has neuroprotective properties that guard against RGC degradation in glaucoma. Several mechanisms have been clarified using modern scientific tools, but many more properties still require additional research [9].

Regarding saffron, its chemical analysis has revealed that it contains more than 150 volatile and aroma-producing chemicals, as well as a number of nonvolatile biologically active ingredients, such as crocetin and zeaxanthin carotenoids, and other alpha- and beta-carotenes [6]. Crocetin, a carotenoid dicarboxylic acid, and crocin appear to be the most powerful antioxidant components of saffron. In fact, the crocin's antiapoptotic activity and improved oxygen diffusivity in mammalian tissues are already known [6]. According to research by Kanakis et al. [119], saffron metabolites directly attach to DNA and cause it to partially conform to beta-DNA, shielding the cell from damage.

Furthermore, it has been demonstrated that saffron has anti-inflammatory properties, such as the ability to inhibit tissue necrosis factor. For this reason, the unusual properties of saffron components may employ several distinct mechanisms of action, ranging from direct regulation of gene expression to antioxidant activity that could be crucial for neuroprotection [6].

This review showed that, in addition to GBE and saffron, many other natural compounds may be useful in preserving RGCs and reducing IOP, thus demonstrating a promising and helpful role in the glaucoma therapy and management. In fact, all analyzed herbal medicines have been proven to be effective or have shown encouraging effects in neuroprotection reducing RGC death, except for Coleus forskohlii.

On the other hand, only Vaccinium myrtillus and Ribes nigrum showed positive and promising effects on decreasing IOP, while all other natural compounds showed either no effects or conflicting results in the various studies, in particular Crocus sativus and Coleus forskohlii (Tables 1 and 2).

Table 1.

Main-demonstrated biological properties of the discussed herbal compounds.

Herbal compounds Biological properties
Ginkgo biloba Vasoactive effects
Hemorheological regulation
Anti-inflammatory effects
Antioxidative capacities
Neuroprotection

Scutellaria baicalensis Georgi Blood pressure, capillary permeability, and serum cholesterol level reduction
Antioxidative effects
Antitumor capacities
Anti-inflammatory effects
Neuroprotection

Crocus sativus L. Antioxidative effects
Anti-inflammatory effects
Antidepressive, anxiolytic, and anticonvulsant capacities
Antiatherogenic, hypolipidemic, and antihypertensive effects
Antitumor actions
Neuroprotection

Coleus forskohlii Basophil and mast cell degranulation inhibition
Histamine release inhibition
Blood pressure and intraocular pressure reduction
Platelet aggregation inhibition
Vasodilation, bronchodilation, and thyroid hormone secretion promotion lipolysis in fat cell stimulation

Vaccinium myrtillus Strong antioxidant properties
Capillary permeability and fragility reduction
Collagen fiber stabilization and collagen biosynthesis promotion
Anti-inflammatory effects
Platelet aggregation inhibition
Blood glucose level reduction

Ribes nigrum L. Antioxidant properties
Capillary permeability and fragility reduction
Collagen fiber stabilization and collagen biosynthesis promotion
Anti-inflammatory effects
Platelet aggregation inhibition
Blood glucose level reduction

Erigeron breviscapus Blood circulation improvement
Antithrombotic effects

Salvia miltiorrhiza Vascular microcirculation improvement

Table 2.

Summary of the main effects of the discussed herbal compounds on retinal ganglion cells and intraocular pressure.

Herbal compounds In vitro or animal studies Human studies Effects on RGCs Effects on IOP
Ginkgo biloba 2 2 Possible reduction of the damage induced by oxidant agents both in animal models and in NTG patients [3033]
No data on POAG patients
Not demonstrated

Scutellaria baicalensis Georgi 4 Strong capacity to protect RGCs from oxidative stress in animal and in vitro models [5254, 56]
No data on human models
Not demonstrated

Crocus sativus L. 1 2 Neuroprotective effects derived from antioxidant and anti-inflammatory effects both in animal models and in POAG patients [65]
No data on NTG patients
Conflicting results from human studies on POAG patients [67, 68]
No data on NTG patients

Coleus forskohlii 3 4 Not demonstrated Conflicting results from studies on animal models, healthy people, and POAG patients [7985]
No data on NTG patients

Vaccinium myrtillus 1 3 Neuroprotective effects through retinal microcirculation improvement both in animal and human models [93] Slight IOP reduction if administered orally in patients with ocular hypertension [9496]
No data on POAG and NTG patients

Ribes nigrum L. 3 Neuroprotective effects through ocular blood flow improvement in POAG patients [97, 98]
No data on NTG patients
IOP decrease both in healthy people and POAG patients [99]
No data on POAG patients

Erigeron breviscapus 1 Stimulating effects in POAG patients with IOP in a controlled range [102]
No data on NTG patients
Not demonstrated

Salvia miltiorrhiza 1 1 Neuroprotective effects on animal model and POAG patients [104, 105]
No data on NTG patients
Not demonstrated

From our analysis, according to the previously published literature [510], it seems that the main beneficial effects of these natural compounds can be attributed to their antioxidant and anti-inflammatory properties, capable of exerting a neuroprotective effect, especially on RGCs.

The present review has several limitations, including the too small number of papers embedded for the predetermined analysis, especially considering the clinical studies performed on human models and glaucomatous patients. In fact, several studies were performed only on healthy volunteers, while no study included both POAG and NTG patients to compare the therapeutic effects of these herbal treatments.

In addition, all included papers have a small sample size, which makes the obtained data less meaningful.

5. Conclusions

In conclusion, the natural compounds analyzed in this review appear to show promising effects, especially on neuroprotection, while they seem to be less effective on IOP decrease. However, further studies are needed to better understand how these herbal compounds can possibly be incorporated into glaucoma therapeutic protocols.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.

References

  • 1.Ritch R. Neuroprotection: is it already applicable to glaucoma therapy? Current Opinion in Ophthalmology . 2000;11(2):78–84. doi: 10.1097/00055735-200004000-00002. [DOI] [PubMed] [Google Scholar]
  • 2.Flammer J., Orgül S., Costa V. P., et al. The impact of ocular blood flow in glaucoma. Progress in Retinal and Eye Research . 2002;21(4):359–393. doi: 10.1016/s1350-9462(02)00008-3. [DOI] [PubMed] [Google Scholar]
  • 3.Brubaker R. F. Delayed functional loss in glaucoma LII Edward Jackson Memorial Lecture. American Journal of Ophthalmology . 1996;121(5):473–483. doi: 10.1016/s0002-9394(14)75421-2. [DOI] [PubMed] [Google Scholar]
  • 4.Rhee D. J., Katz L. J., Spaeth G. L., Myers J. S. Complementary and alternative medicine for glaucoma. Survey of Ophthalmology . 2001;46(1):43–55. doi: 10.1016/s0039-6257(01)00233-8. [DOI] [PubMed] [Google Scholar]
  • 5.Maiuolo J., Bulotta R. M., Oppedisano F., et al. Potential properties of natural nutraceuticals and antioxidants in age-related eye disorders. Life . 2022;13(1):p. 77. doi: 10.3390/life13010077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Medori M. C., Naureen Z., Dhuli K., Placidi G., Falsini B., Bertelli M. Dietary supplements in retinal diseases, glaucoma, and other ocular conditions. Journal of Preventive Medicine and Hygiene . 2022;63(2) Supplement 3:E189–E199. doi: 10.15167/2421-4248/jpmh2022.63.2S3.2760. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Chaudhry S., Dunn H., Carnt N., White A. Nutritional supplementation in the prevention and treatment of glaucoma. Survey of Ophthalmology . 2022;67(4):1081–1098. doi: 10.1016/j.survophthal.2021.12.001. [DOI] [PubMed] [Google Scholar]
  • 8.Ige M., Liu J. Herbal medicines in glaucoma treatment. The Yale Journal of Biology and Medicine . 2020;93(2):347–353. [PMC free article] [PubMed] [Google Scholar]
  • 9.Mi X. S., Zhong J. X., Chang R. C., So K. F. Research advances on the usage of traditional Chinese medicine for neuroprotection in glaucoma. Journal of Integrative Medicine . 2013;11(4):233–240. doi: 10.3736/jintegrmed2013037. [DOI] [PubMed] [Google Scholar]
  • 10.Wilkinson J. T., Fraunfelder F. W. Use of herbal medicines and nutritional supplements in ocular disorders: an evidence-based review. Drugs . 2011;71(18):2421–2434. doi: 10.2165/11596840-000000000-00000. [DOI] [PubMed] [Google Scholar]
  • 11.Binns C. W., Lee M. K., Lee A. H. Problems and prospects: public health regulation of dietary supplements. Annual Review of Public Health . 2018;39(1):403–420. doi: 10.1146/annurev-publhealth-040617-013638. [DOI] [PubMed] [Google Scholar]
  • 12.Thomson P., Jones J., Browne M., Leslie S. J. Why people seek complementary and alternative medicine before conventional medical treatment: a population based study. Complementary Therapies in Clinical Practice . 2014;20(4):339–346. doi: 10.1016/j.ctcp.2014.07.008. [DOI] [PubMed] [Google Scholar]
  • 13.Hostettmann K., Wolfender J.-L. The search for biologically active secondary metabolites. Pesticide Science . 1997;51(4):471–482. doi: 10.1002/(SICI)1096-9063(199712)51:4&#x0003c;471::AID-PS662&#x0003e;3.0.CO;2-S. [DOI] [Google Scholar]
  • 14.Soejarto D. D. Biodiversity prospecting and benefit-sharing: perspectives from the field. Journal of Ethnopharmacology . 1996;51(1-3):1–15. doi: 10.1016/0378-8741(95)01345-8. [DOI] [PubMed] [Google Scholar]
  • 15.Labkovich M., Jacobs E. B., Bhargava S., Pasquale L. R., Ritch R. Ginkgo biloba extract in ophthalmic and systemic disease, with a focus on normal-tension glaucoma. Asia-pacific Journal of Ophthalmology . 2020;9(3):215–225. doi: 10.1097/APO.0000000000000279. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Ritch R. Potential role for Ginkgo biloba extract in the treatment of glaucoma. Medical Hypotheses . 2000;54(2):221–235. doi: 10.1054/mehy.1999.0025. [DOI] [PubMed] [Google Scholar]
  • 17.Koltermann A., Hartkorn A., Koch E., Fürst R., Vollmar A. M., Zahler S. Ginkgo biloba extract EGb® 761 increases endothelial nitric oxide production in vitro and in vivo. Cellular and Molecular Life Sciences . 2007;64(13):1715–1722. doi: 10.1007/s00018-007-7085-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Kubota Y., Tanaka N., Kagota S., et al. Effects of Ginkgo biloba extract on blood pressure and vascular endothelial response by acetylcholine in spontaneously hypertensive rats. The Journal of Pharmacy and Pharmacology . 2006;58(2):243–249. doi: 10.1211/jpp.58.2.0012. [DOI] [PubMed] [Google Scholar]
  • 19.Huang S.-Y., Jeng C., Kao S.-C., Yu J. J.-H., Liu D.-Z. Improved haemorrheological properties by Ginkgo biloba extract (Egb 761) in type 2 diabetes mellitus complicated with retinopathy. Clinical Nutrition . 2004;23(4):615–621. doi: 10.1016/j.clnu.2003.10.010. [DOI] [PubMed] [Google Scholar]
  • 20.Naderi G. A., Asgary S., Jafarian A., Askari N., Behagh A., Aghdam R. H. Fibrinolytic effects of Ginkgo biloba extract. Experimental and Clinical Cardiology . 2005;10(2):85–87. [PMC free article] [PubMed] [Google Scholar]
  • 21.Cheng S. M., Yang S. P., Ho L. J., et al. Down-regulation of c- jun N-terminal kinase-activator protein-1 signaling pathway by Ginkgo biloba extract in human peripheral blood T cells. Biochemical Pharmacology . 2003;66(4):679–689. doi: 10.1016/s0006-2952(03)00388-5. [DOI] [PubMed] [Google Scholar]
  • 22.Ilieva I., Ohgami K., Shiratori K., et al. The effects of Ginkgo biloba extract on lipopolysaccharide-induced inflammation in vitro and in vivo. Experimental Eye Research . 2004;79(2):181–187. doi: 10.1016/j.exer.2004.03.009. [DOI] [PubMed] [Google Scholar]
  • 23.Kwak W. J., Han C. K., Son K. H., et al. Effects of Ginkgetin from Ginkgo biloba leaves on cyclooxygenases and in vivo skin inflammation. Planta Medica . 2002;68(4):316–321. doi: 10.1055/s-2002-26742. [DOI] [PubMed] [Google Scholar]
  • 24.Wang J., Zheng M., Chen L., et al. Rapid screening, separation, and detection of hydroxyl radical scavengers from total flavonoids of Ginkgo biloba leaves by chromatography combined with molecular devices. Journal of Separation Science . 2016;39(21):4158–4165. doi: 10.1002/jssc.201600679. [DOI] [PubMed] [Google Scholar]
  • 25.Birks J., Grimley E. J. Ginkgo biloba for cognitive impairment and dementia. Cochrane Database of Systematic Reviews . 2009;1, article CD003120 doi: 10.1002/14651858.CD003120.pub3. [DOI] [PubMed] [Google Scholar]
  • 26.Ghiso J. A., Doudevski I., Ritch R., Rostagno A. A. Alzheimer’s disease and glaucoma: mechanistic similarities and differences. Journal of Glaucoma . 2013;22(5):S36–S38. doi: 10.1097/IJG.0b013e3182934af6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Kong G. Y. X., Van Bergen N. J., Trounce I. A., Crowston J. G. Mitochondrial dysfunction and glaucoma. Journal of Glaucoma . 2009;18(2):93–100. doi: 10.1097/IJG.0b013e318181284f. [DOI] [PubMed] [Google Scholar]
  • 28.Saccà S. C., Pascotto A., Camicione P., Capris P., Izzotti A. Oxidative DNA damage in the human trabecular meshwork: clinical correlation in patients with primary open-angle glaucoma. Archives of Ophthalmology . 2005;123(4):458–463. doi: 10.1001/archopht.123.4.458. [DOI] [PubMed] [Google Scholar]
  • 29.Eckert A., Keil U., Scherping I., Hauptmann S., Müller W. E. Stabilization of mitochondrial membrane potential and improvement of neuronal energy metabolism by Ginkgo biloba extract EGb 761. Annals of the New York Academy of Sciences . 2005;1056(1):474–485. doi: 10.1196/annals.1352.023. [DOI] [PubMed] [Google Scholar]
  • 30.Cho H.-K., Kim S., Lee E. J., Kee C. Neuroprotective effect of ginkgo biloba extract against hypoxic retinal ganglion cell degeneration in vitro and in vivo. Journal of Medicinal Food . 2019;22(8):771–778. doi: 10.1089/jmf.2018.4350. [DOI] [PubMed] [Google Scholar]
  • 31.Hirooka K., Tokuda M., Miyamoto O., Itano T., Baba T., Shiraga F. The Ginkgo biloba extract (EGb 761) provides a neuro-protective effect on retinal ganglion cells in a rat model of chronic glaucoma. Current Eye Research . 2004;28(3):153–157. doi: 10.1076/ceyr.28.3.153.26246. [DOI] [PubMed] [Google Scholar]
  • 32.Guo X., Kong X., Huang R., et al. Effect of Ginkgo biloba on visual field and contrast sensitivity in Chinese patients with normal tension glaucoma: a randomized, crossover clinical trial. Investigative Ophthalmology & Visual Science . 2014;55(1):110–116. doi: 10.1167/iovs.13-13168. [DOI] [PubMed] [Google Scholar]
  • 33.Lee J., Sohn S. W., Kee C. Effect of Ginkgo biloba extract on visual field progression in normal tension glaucoma. Journal of Glaucoma . 2013;22(9):780–784. doi: 10.1097/IJG.0b013e3182595075. [DOI] [PubMed] [Google Scholar]
  • 34.Kimuya Y., Kubo M., Tani T., Arichi S. Studies on Scutellariae radix. IV. Effect on lipid peroxidation in rat liver. Chemical and Pharmaceutical Bulletin . 1981;29(9):2610–2617. doi: 10.1248/cpb.29.2610. [DOI] [PubMed] [Google Scholar]
  • 35.Kubo M., Matsuda H., Tanaka M., et al. Studies on Scutellariae radix. VII. Anti-arthritic and anti-inflammatory actions of methanolic extract and flavonoid components from Scutellariae radix. Chemical and Pharmaceutical Bulletin . 1984;32(7):2724–2729. doi: 10.1248/cpb.32.2724. [DOI] [PubMed] [Google Scholar]
  • 36.Lee I. S., Park S., Park K., Choue R. Hepatoprotective activity of scutellariae radix extract in mice fed a high fat diet with chronic alcohol exposure. Phytotherapy Research . 2011;25(9):1348–1353. doi: 10.1002/ptr.3370. [DOI] [PubMed] [Google Scholar]
  • 37.Xin H. G., Zhang B. B., Wu Z. Q., et al. Treatment with baicalein attenuates methionine−choline deficient diet-induced non-alcoholic steatohepatitis in rats. European Journal of Pharmacology . 2014;738:310–318. doi: 10.1016/j.ejphar.2014.06.006. [DOI] [PubMed] [Google Scholar]
  • 38.Wang Y.-H., Yu H.-T., Pu X.-P., Du G.-H. Baicalein prevents 6-hydroxydopamine-induced mitochondrial dysfunction in SH-SY5Y cells via inhibition of mitochondrial oxidation and up-regulation of DJ-1 protein expression. Molecules . 2013;18(12):14726–14738. doi: 10.3390/molecules181214726. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Yu C., Zhang Z., Zhang H., et al. Pretreatment of baicalin and wogonoside with glycoside hydrolase: a promising approach to enhance anticancer potential. Oncology Reports . 2013;30(5):2411–2418. doi: 10.3892/or.2013.2726. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Yeh C. H., Shih H. C., Hong H. M., et al. Protective effect of wogonin on proinflammatory cytokine generation via Jak 1/3-STAT1/3 pathway in lipopolysaccharide stimulated BV2 microglial cells. Toxicology and Industrial Health . 2015;31(10):960–966. doi: 10.1177/0748233713485886. [DOI] [PubMed] [Google Scholar]
  • 41.Zheng W. X., Wang F., Cao X. L., et al. Baicalin protects PC-12 cells from oxidative stress induced by hydrogen peroxide via anti-apoptotic effects. Brain Injury . 2014;28(2):227–234. doi: 10.3109/02699052.2013.860469. [DOI] [PubMed] [Google Scholar]
  • 42.Zhang S., Ye J., Dong G. Neuroprotective effect of baicalein on hydrogen peroxide-mediated oxidative stress and mitochondrial dysfunction in PC12 cells. Journal of Molecular Neuroscience . 2010;40(3):311–320. doi: 10.1007/s12031-009-9285-5. [DOI] [PubMed] [Google Scholar]
  • 43.Wakabayashi I. Inhibitory effects of baicalein and wogonin on lipopolysaccharide-induced nitric oxide production in macrophages. Pharmacology & Toxicology . 1999;84(6):288–291. doi: 10.1111/j.1600-0773.1999.tb01496.x. [DOI] [PubMed] [Google Scholar]
  • 44.Chen Y. C., Shen S. C., Chen L. G., Lee T. J., Yang L. L. Wogonin, baicalin, and baicalein inhibition of inducible nitric oxide synthase and cyclooxygenase-2 gene expressions induced by nitric oxide synthase inhibitors and lipopolysaccharide1. Biochemical Pharmacology . 2001;61(11):1417–1427. doi: 10.1016/s0006-2952(01)00594-9. [DOI] [PubMed] [Google Scholar]
  • 45.Chi Y. S., Lim H., Park H., Kim H. P. Effects of wogonin, a plant flavone from Scutellaria radix, on skin inflammation: in vivo regulation of inflammation-associated gene expression. Biochemical Pharmacology . 2003;66(7):1271–1278. doi: 10.1016/s0006-2952(03)00463-5. [DOI] [PubMed] [Google Scholar]
  • 46.Hsieh C. J., Hall K., Ha T., Li C., Krishnaswamy G., Chi D. S. Baicalein inhibits IL-1β- and TNF-α-induced inflammatory cytokine production from human mast cells via regulation of the NF-κB pathway. Clinical and Molecular Allergy . 2007;5(1) doi: 10.1186/1476-7961-5-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Hou J., Wang J., Zhang P., et al. Baicalin attenuates proinflammatory cytokine production in oxygen-glucose deprived challenged rat microglial cells by inhibiting TLR4 signaling pathway. International Immunopharmacology . 2012;14(4):749–757. doi: 10.1016/j.intimp.2012.10.013. [DOI] [PubMed] [Google Scholar]
  • 48.Takai Y., Tanito M., Ohira A. Multiplex cytokine analysis of aqueous humor in eyes with primary open-angle glaucoma, ex-foliation glaucoma, and cataract. Investigative Ophthalmology & Visual Science . 2012;53(1):241–247. doi: 10.1167/iovs.11-8434. [DOI] [PubMed] [Google Scholar]
  • 49.Gao Z., Huang K., Yang X., Xu H. Free radical scavenging and antioxidant activities of flavonoids extracted from the radix of Scutellaria baicalensis Georgi. Biochimica et Biophysica Acta . 1999;1472(3):643–650. doi: 10.1016/s0304-4165(99)00152-x. [DOI] [PubMed] [Google Scholar]
  • 50.Shieh D. E., Liu L. T., Lin C. C. Antioxidant and free radical scavenging effects of baicalein, baicalin and wogonin. Anticancer Research . 2000;20(5A):2861–2865. [PubMed] [Google Scholar]
  • 51.Perez C. A., Wei Y., Guo M. Iron-binding and anti-Fenton properties of baicalein and baicalin. Journal of Inorganic Biochemistry . 2009;103(3):326–332. doi: 10.1016/j.jinorgbio.2008.11.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Maher P., Hanneken A. Flavonoids protect retinal ganglion cells from oxidative stress-induced death. Investigative Ophthalmology & Visual Science . 2005;46(12):4796–4803. doi: 10.1167/iovs.05-0397. [DOI] [PubMed] [Google Scholar]
  • 53.Jung S. H., Kang K. D., Ji D., et al. The flavonoid baicalin counteracts ischemic and oxidative insults to retinal cells and lipid peroxidation to brain membranes. Neurochemistry International . 2008;53(6-8):325–337. doi: 10.1016/j.neuint.2008.09.004. [DOI] [PubMed] [Google Scholar]
  • 54.Gong L., Zhu J. Baicalin alleviates oxidative stress damage in trabecular meshwork cells in vitro. Naunyn-Schmiedeberg's Archives of Pharmacology . 2018;391(1):51–58. doi: 10.1007/s00210-017-1433-9. [DOI] [PubMed] [Google Scholar]
  • 55.Ishige K., Schubert D., Sagara Y. Flavonoids protect neuronal cells from oxidative stress by three distinct mechanisms. Free Radical Biology & Medicine . 2001;30(4):433–446. doi: 10.1016/s0891-5849(00)00498-6. [DOI] [PubMed] [Google Scholar]
  • 56.Xu Y., Yang B., Hu Y., et al. Wogonin prevents TLR4-NF-κB-medicated neuro-inflammation and improves retinal ganglion cells survival in retina after optic nerve crush. Oncotarget . 2016;7(45):72503–72517. doi: 10.18632/oncotarget.12700. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.José Bagur M., Alonso Salinas G. L., Jiménez-Monreal A. M., et al. Saffron: an old medicinal plant and a potential novel functional food. Molecules . 2018;23(1):p. 30. doi: 10.3390/molecules23010030. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Christodoulou E., Kadoglou N. P. E., Kostomitsopoulos N., Valsami G. Saffron: a natural product with potential pharmaceutical applications. The Journal of Pharmacy and Pharmacology . 2015;67(12):1634–1649. doi: 10.1111/jphp.12456. [DOI] [PubMed] [Google Scholar]
  • 59.Hosseini A., Razavi B. M., Hosseinzadeh H. Saffron (Crocus sativus) petal as a new pharmacological target: a review. Iranian Journal of Basic Medical Sciences . 2018;21(11):1091–1099. doi: 10.22038/IJBMS.2018.31243.7529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Ghaffari S., Roshanravan N. Saffron; an updated review on biological properties with special focus on cardiovascular effects. Biomedicine & Pharmacotherapy . 2019;109:21–27. doi: 10.1016/j.biopha.2018.10.031. [DOI] [PubMed] [Google Scholar]
  • 61.Poma A., Fontecchio G., Carlucci G., Chichiriccò G. Anti-inflammatory properties of drugs from saffron crocus. Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry . 2012;11(1):37–51. doi: 10.2174/187152312803476282. [DOI] [PubMed] [Google Scholar]
  • 62.Ishizuka F., Shimazawa M., Umigai N., et al. Crocetin, a carotenoid derivative, inhibits retinal ischemic damage in mice. European Journal of Pharmacology . 2013;703(1-3):1–10. doi: 10.1016/j.ejphar.2013.02.007. [DOI] [PubMed] [Google Scholar]
  • 63.Qi Y., Chen L., Zhang L., Liu W. B., Chen X. Y., Yang X. G. Crocin prevents retinal ischaemia/reperfusion injury-induced apoptosis in retinal ganglion cells through the PI3K/AKT signalling pathway. Experimental Eye Research . 2013;107:44–51. doi: 10.1016/j.exer.2012.11.011. [DOI] [PubMed] [Google Scholar]
  • 64.Chen L., Qi Y., Yang X. Neuroprotective effects of crocin against oxidative stress induced by ischemia/reperfusion injury in rat retina. Ophthalmic Research . 2015;54(3):157–168. doi: 10.1159/000439026. [DOI] [PubMed] [Google Scholar]
  • 65.Fernández-Albarral J. A., Ramírez A. I., de Hoz R., et al. Neuroprotective and anti-inflammatory effects of a hydrophilic saffron extract in a model of glaucoma. International Journal of Molecular Sciences . 2019;20(17):p. 4110. doi: 10.3390/ijms20174110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Haynes S. E., Hollopeter G., Yang G., et al. The P2Y12 receptor regulates microglial activation by extracellular nucleotides. Nature Neuroscience . 2006;9(12):1512–1519. doi: 10.1038/nn1805. [DOI] [PubMed] [Google Scholar]
  • 67.Hecht I., Achiron A., Bartov E., et al. Effects of dietary and lifestyle recommendations on patients with glaucoma: a randomized controlled pilot trial. European Journal of Integrative Medicine . 2019;25:60–66. doi: 10.1016/j.eujim.2018.12.002. [DOI] [Google Scholar]
  • 68.Jabbarpoor Bonyadi M. H., Yazdani S., Saadat S. The ocular hypotensive effect of saffron extract in primary open angle glaucoma: a pilot study. BMC Complementary and Alternative Medicine . 2014;14(1) doi: 10.1186/1472-6882-14-399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Metzger H., Lindner E. The positive inotropic-acting forskolin, a potent adenylate cyclase activator. Arzneimittel-Forschung . 1981;31(8):1248–1250. [PubMed] [Google Scholar]
  • 70.Marone G., Columbo M., Triggiani M., Vigorita S., Formisano S. Forskolin inhibits the release of histamine from human basophils and mast cells. Agents and Actions . 1986;18(1-2):96–99. doi: 10.1007/BF01987993. [DOI] [PubMed] [Google Scholar]
  • 71.Dubey M. P., Srimal R. C., Nityanand S., Dhawan B. N. Pharmacological studies on coleonol, a hypotensive diterpene from Coleus forskohlii. Journal of Ethnopharmacology . 1981;3(1):1–13. doi: 10.1016/0378-8741(81)90010-6. [DOI] [PubMed] [Google Scholar]
  • 72.Caprioli J., Sears M., Bausher L., Gregory D., Mead A. Forskolin lowers intraocular pressure by reducing aqueous inflow. Investigative Ophthalmology & Visual Science . 1984;25(3):268–277. [PubMed] [Google Scholar]
  • 73.Wong S., Mok W., Phaneuf S., Katz S., Salari H. Forskolin inhibits platelet-activating factor binding to platelet receptors independently of adenylyl cyclase activation. European Journal of Pharmacology . 1993;245(1):55–61. doi: 10.1016/0922-4106(93)90169-a. [DOI] [PubMed] [Google Scholar]
  • 74.Wysham D. G., Brotherton A. F., Heistad D. D. Effects of forskolin on cerebral blood flow: implications for a role of adenylate cyclase. Stroke . 1986;17(6):1299–1303. doi: 10.1161/01.str.17.6.1299. [DOI] [PubMed] [Google Scholar]
  • 75.Lichey I., Friedrich T., Priesnitz M., Biamino G., Usinger P., Huckauf H. Effect of forskolin on methacholine-induced bronchoconstriction in extrinsic asthmatics. The Lancet . 1984;2(8395):p. 167. doi: 10.1016/s0140-6736(84)91084-5. [DOI] [PubMed] [Google Scholar]
  • 76.Roger P. P., Servais P., Dumont J. E. Regulation of dog thyroid epithelial cell cycle by forskolin, an adenylate cyclase activator. Experimental Cell Research . 1987;172(2):282–292. doi: 10.1016/0014-4827(87)90387-9. [DOI] [PubMed] [Google Scholar]
  • 77.Okuda H., Morimoto C., Tsujita T. Relationship between cyclic AMP production and lipolysis induced by forskolin in rat fat cells. Journal of Lipid Research . 1992;33(2):225–231. doi: 10.1016/S0022-2275(20)41542-1. [DOI] [PubMed] [Google Scholar]
  • 78.Mills I., Moreno F. J., Fain J. N. Forskolin inhibition of glucose metabolism in rat adipocytes independent of adenosine 3’,5’-monophosphate accumulation and lipolysis. Endocrinology . 1984;115(3):1066–1069. doi: 10.1210/endo-115-3-1066. [DOI] [PubMed] [Google Scholar]
  • 79.Zeng S., Shen B., Wen L., et al. Experimental studies of the effect of forskolin on the lowering of intraocular pressure. Yan Ke Xue Bao . 1995;11(3):173–176. [PubMed] [Google Scholar]
  • 80.Lee P. Y., Podos S. M., Serle J. B., Camras C. B., Severin C. H. Intraocular pressure effects of multiple doses of drugs applied to glaucomatous monkey eyes. Archives of Ophthalmology . 1987;105(2):249–252. doi: 10.1001/archopht.1987.01060020103038. [DOI] [PubMed] [Google Scholar]
  • 81.Caprioli J., Sears M. Forskolin lowers intraocular pressure in rabbits, monkeys, and man. The Lancet . 1983;1(8331):958–960. doi: 10.1016/s0140-6736(83)92084-6. [DOI] [PubMed] [Google Scholar]
  • 82.Meyer B. H., Stulting A. A., Müller F. O., Luus H. G., Badian M. The effects of forskolin eye drops on intra-ocular pressure. South African Medical Journal . 1987;71(9):570–571. [PubMed] [Google Scholar]
  • 83.Seto C., Eguchi S., Araie M., Matsumoto S., Takase M. Acute effects of topical forskolin on aqueous humor dynamics in man. Japanese Journal of Ophthalmology . 1986;30(3):238–244. [PubMed] [Google Scholar]
  • 84.Brubaker R. F., Carlson K. H., Kullerstrand L. J., McLaren J. W. Topical forskolin (colforsin) and aqueous flow in humans. Archives of Ophthalmology . 1987;105(5):637–641. doi: 10.1001/archopht.1987.01060050055037. [DOI] [PubMed] [Google Scholar]
  • 85.Mutolo M. G., Albanese G., Rusciano D., Pescosolido N. Oral administration of forskolin, homotaurine, carnosine, and folic acid in patients with primary open angle glaucoma: changes in intraocular pressure, pattern electroretinogram amplitude, and foveal sensitivity. Journal of Ocular Pharmacology and Therapeutics . 2016;32(3):178–183. doi: 10.1089/jop.2015.0121. [DOI] [PubMed] [Google Scholar]
  • 86.Head K. A. Natural therapies for ocular disorders, part two: cataracts and glaucoma. Alternative Medicine Review . 2001;6(2):141–166. [PubMed] [Google Scholar]
  • 87.Salvayre R. Flavonoids and Bioflavonoids 1981 . Elsevier Press; 1982. [Google Scholar]
  • 88.Mian E., Curri S. B., Lietti A., Bombardelli E. Anthocyanosides and the walls of the microvessels: further aspects of the mechanism of action of their protective effect in syndromes due to abnormal capillary fragility. Minerva Medica . 1977;68(52):3565–3581. [PubMed] [Google Scholar]
  • 89.Havsteen B. Flavonoids, a class of natural products of high pharmacological potency. Biochemical Pharmacology . 1983;32(7):1141–1148. doi: 10.1016/0006-2952(83)90262-9. [DOI] [PubMed] [Google Scholar]
  • 90.Amella M., Bronner C., Briancon F., Haag M., Anton R., Landry Y. Inhibition of mast cell histamine release by flavonoids and biflavonoids. Planta Medica . 1985;51(1):16–20. doi: 10.1055/s-2007-969381. [DOI] [PubMed] [Google Scholar]
  • 91.Bottecchia D. Preliminary reports on the inhibitory effect of Vaccinium myrtillus anthocyanosides on platelet aggregation and clot retraction. Fitoterapia . 1987;48:3–8. [Google Scholar]
  • 92.Bever B. O., Zahnd G. R. Plants with oral hypoglycaemic action. Quarterly Journal of Crude Drug Research . 1979;17(3-4):139–196. doi: 10.3109/13880207909065167. [DOI] [Google Scholar]
  • 93.Nakamura O., Moritoh S., Sato K., et al. Bilberry extract administration prevents retinal ganglion cell death in mice via the regulation of chaperone molecules under conditions of endoplasmic reticulum stress. Clinical Ophthalmology . 2017;11:1825–1834. doi: 10.2147/OPTH.S145159. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 94.Caselli L. Clinical and electroretinographic study on activity of anthocyanosides. Archivio di Medicina Interna . 1985;37:29–35. [Google Scholar]
  • 95.Shim S. H., Kim J. M., Choi C. Y., Kim C. Y., Park K. H. Ginkgo biloba extract and bilberry anthocyanins improve visual function in patients with normal tension glaucoma. Journal of Medicinal Food . 2012;15(9):818–823. doi: 10.1089/jmf.2012.2241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Gizzi C., Torino-Rodriguez P., Belcaro G., Hu S., Hosoi M., Feragalli B. Mirtogenol® supplementation in association with dorzolamide-timolol or latanoprost improves the retinal microcirculation in asymptomatic patients with increased ocular pressure. European Review for Medical and Pharmacological Sciences . 2017;21(20):4720–4725. [PubMed] [Google Scholar]
  • 97.Ohguro H., Ohguro I., Katai M., Tanaka S. Two-year randomized, placebo-controlled study of black currant anthocyanins on visual field in glaucoma. Ophthalmologica . 2012;228(1):26–35. doi: 10.1159/000335961. [DOI] [PubMed] [Google Scholar]
  • 98.Yoshida K., Ohguro I., Ohguro H. Black currant anthocyanins normalized abnormal levels of serum concentrations of endothelin-1 in patients with glaucoma. Journal of Ocular Pharmacology and Therapeutics . 2013;29(5):480–487. doi: 10.1089/jop.2012.0198. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 99.Ohguro H., Ohguro I., Yagi S. Effects of black currant anthocyanins on intraocular pressure in healthy volunteers and patients with glaucoma. Journal of Ocular Pharmacology and Therapeutics . 2013;29(1):61–67. doi: 10.1089/jop.2012.0071. [DOI] [PubMed] [Google Scholar]
  • 100.Wang Z. Y., Chen D. C., He Y., Ruan C. G., Zhang R. W. Differential effects of new breviscapine on arachidonic acid metabolisms in blood cells and endothelial cells. Zhongguo Yao Li Xue Bao . 1993;14(2):148–151. [PubMed] [Google Scholar]
  • 101.Zhou Q. S., Zhao Y. M., Bai X., Li P. X., Ruan C. G. Effect of new-breviscapine on fibrinolysis and anticoagulation of human vascular endothelial cells. Zhongguo Yao Li Xue Bao . 1992;13(3):239–242. [PubMed] [Google Scholar]
  • 102.Zhong Y., Xiang M., Ye W., Cheng Y., Jiang Y. Visual field protective effect of Erigeron breviscapus (vant.) Hand. Mazz. extract on glaucoma with controlled intraocular pressure: a randomized, double-blind, clinical trial. Drugs in R & D . 2010;10(2):75–82. doi: 10.2165/11539090-000000000-00000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Cheng T. O. Cardiovascular effects of danshen. International Journal of Cardiology . 2007;121(1):9–22. doi: 10.1016/j.ijcard.2007.01.004. [DOI] [PubMed] [Google Scholar]
  • 104.Zhu M. D., Cai F. Y. Evidence of compromised circulation in the pathogenesis of optic nerve damage in chronic glaucomatous rabbit. Chinese Medical Journal . 1993;106(12):922–927. [PubMed] [Google Scholar]
  • 105.Zhu Q., Su G., Nie L., Wang C., He Y., Liu X. Salvia miltiorrhiza extracts protect against retinal injury in a rat glaucoma model. Experimental and Therapeutic Medicine . 2014;7(6):1513–1515. doi: 10.3892/etm.2014.1632. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Wu Z. Z., Jiang Y. Q., Yi S. M., Xia M. T. Radix Salviae miltiorrhizae in middle and late stage glaucoma. Chinese Medical Journal . 1983;96(6):445–447. [PubMed] [Google Scholar]
  • 107.De Bernardo M., Capasso L., Caliendo L., Vosa Y., Rosa N. Intraocular pressure evaluation after myopic refractive surgery: a comparison of methods in 121 eyes. Seminars in Ophthalmology . 2016;31(3):233–242. doi: 10.3109/08820538.2014.962156. [DOI] [PubMed] [Google Scholar]
  • 108.De Bernardo M., Borrelli M., Cembalo G., Rosa N. Intraocular pressure measurements in standing position with a rebound tonometer. Medicina . 2019;55(10):p. 701. doi: 10.3390/medicina55100701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 109.De Bernardo M., Vitiello L., Rosa N. Optic nerve ultrasonography to predict increased intracranial pressure in idiopathic intracranial hypertension. The Neuroradiology Journal . 2019;32(3):227–228. doi: 10.1177/1971400919832001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.De Bernardo M., Vitiello L. Optic nerve ultrasound measurement in multiple sclerosis. Acta Neurologica Scandinavica . 2019;139(4):399–400. doi: 10.1111/ane.13072. [DOI] [PubMed] [Google Scholar]
  • 111.De Bernardo M., Cembalo G., Rosa N. Reliability of intraocular pressure measurement by Goldmann applanation tonometry after refractive surgery: a review of different correction formulas. Clinical Ophthalmology . 2020;14:2783–2788. doi: 10.2147/OPTH.S263856. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112.De Bernardo M., Salerno G., Gioia M., et al. Intraocular pressure and choroidal thickness postural changes in multiple system atrophy and Parkinson's disease. Scientific Reports . 2021;11(1):p. 8936. doi: 10.1038/s41598-021-88250-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 113.De Bernardo M., Casaburi C., De Pascale I., Capasso L., Cione F., Rosa N. Comparison between dynamic contour tonometry and Goldmann applanation tonometry correcting equations. Scientific Reports . 2022;12(1, article 20190) doi: 10.1038/s41598-022-24318-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 114.De Bernardo M., Abbinante G., Borrelli M., Di Stasi M., Cione F., Rosa N. Intraocular pressure measurements in standing, sitting, and supine position: comparison between Tono-Pen Avia and Icare Pro Tonometers. Journal of Clinical Medicine . 2022;11(21):p. 6234. doi: 10.3390/jcm11216234. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115.Zhang Y. Y., Li Z. D., Jiang N., et al. The effects and mechanism of baicalin in a mouse acute hypertensive glaucoma model. Zhonghua Yan Ke Za Zhi . 2020;56(5):376–382. doi: 10.3760/cma.j.cn112142-20200107-00011. [DOI] [PubMed] [Google Scholar]
  • 116.Zhou W. B., Peng D. W., Chen X. Q., Zeng S. J., Qiu P. X., Hu B. R. Studies on ding gong teng in lowering of intraocular pressure and miosis. Yan Ke Xue Bao . 1986;2(3):150–153. [PubMed] [Google Scholar]
  • 117.Zhu M. D., Cai F. Y. The effect of Inj. Salviae Miltiorrhizae Co. on the retrograde axoplasmic transport in the optic nerve of rabbits with chronic IOP elevation. Zhonghua Yan Ke Za Zhi . 1991;27(3):174–178. [PubMed] [Google Scholar]
  • 118.Wang Z. Y., Mo X. F., Jiang X. H., Rong X. F., Miao H. M. Ginkgolide B promotes axonal growth of retina ganglion cells by anti-apoptosis in vitro. Sheng Li Xue Bao . 2012;64(4):417–424. [PubMed] [Google Scholar]
  • 119.Kanakis C. D., Tarantilis P. A., Tajimir-Riahi H. A., Polissiou M. G. Crocetin, dimethylcrocetin, and safranal bind human serum albumin: stability and antioxidative properties. Journal of Agricultural and Food Chemistry . 2007;55(3):970–977. doi: 10.1021/jf062638l. [DOI] [PubMed] [Google Scholar]

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