A Review of Herbal Therapy in Multiple Sclerosis
Abstract
Multiple sclerosis is a complex autoimmune disorder which characterized by demyelination and axonal loss in the central nervous system (CNS). Several evidences indicate that some new drugs and stem cell therapy have opened a new horizon for multiple sclerosis treatment, but current therapies are partially effective or not safe in the long term. Recently, herbal therapies represent a promising therapeutic approach for multiple sclerosis disease. Here, we consider the potential benefits of some herbal compounds on different aspects of multiple sclerosis disease. The medicinal plants and their derivatives; Ginkgo biloba, Zingiber officinale, Curcuma longa, Hypericum perforatum, Valeriana officinalis, Vaccinium macrocarpon, Nigella sativa,Piper methysticum, Crocus sativus, Panax ginseng, Boswellia papyrifera, Vitis vinifera, Gastrodia elata, Camellia sinensis, Oenothera biennis, MS14 and Cannabis sativa have been informed to have several therapeutic effects in MS patients.
Article type: Review Article
Keywords: Multiple sclerosis, Inflammation, Demyelination, Remyelination, Herbal therapy
Affiliations: Young Researchers and Elite Club, Behshahr Branch, Islamic Azad University, Behshahr, Iran.; Department of Anatomy & Cell Biology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.; Cellular and Molecular Research Center, Department of Anatomy & Cell Biology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.; Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.; Pharmaceutical Sciences Research Center, School of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.; Immunogenetic Research Center, Department of Anatomy & Cell Biology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
License: ©2018 The Authors. CC BY 4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution (CC BY), which permits unrestricted use, distribution, and reproduction in any medium, as long as the original authors and source are cited. No permission is required from the authors or the publishers.
Article links: DOI: 10.15171/apb.2018.066 | PubMed: 30607330 | PMC: PMC6311642
Relevance: Moderate: mentioned 3+ times in text
Full text: PDF (781 KB)
Introduction
Multiple sclerosis (MS) is an autoimmune disease that mostly occurs in young adulthood.1 The etiology of MS disease is still not well understood, but both genetic and environmental factors were found to have important roles in MS disease initiation or progression.2 In MS disease, inflammatory cells demolish myelin sheath in the CNS which weakens action potential conduction.3 Two cardinal properties of MS are acute inflammation that associated with demyelination and another one is axonal loss.4 After injury, oligodendrocyte precursor cells (OPCs) which are residing at parenchyma continuously produce myelinating oligodendrocytes.3–5 In addition, regarding to the ability of neural stem cells for differentiation to OPCs, these stem cells are considered as an important source for remyelination.6–8 These endogenous stem cells proliferate, migrate and differentiate to OPCs after brain injuries. However, endogenous OPCs can produce myelin and improve some aspects of the MS disease, but endogenous repair may fail in long term.7,9 Therefore, several studies have focused on different approaches (including targeting specific signaling pathways, stem cell therapy, suppressing the inflammation process and reprogramming of glial cells to OPCs …) that improve myelination.10 Despite the potential benefits of stem cell therapy in the improvement of myelin repair,11 its clinical application has been hampered because of the possibility of teratoma formation, cell rejection and ethical problems.12,13 Therefore, there is still a need for developing new drugs which have no or less considerable side effects.
The pathophysiology of MS is not well elucidated, which makes itsʼ treatment strategy very difficult and perplexing.14 At the present time, most of the strategies in MS treatment are focused on preventing of inflammation in the CNS.15 Interferon beta (IFN-beta) was firstly confirmed as an effective drug for treatment of MS in 1993.16 Afterward, different drugs were introduced for curing MS such as glatiramer acetate, natalizumab, alemtuzumab and fingolimod.14 All of these mentioned drugs were partially effective and their remarkable adverse effects makes them unsuitable for proloned use.17 For example, several studies indicated the adverse effects of IFN-beta consumption including, stroke, headache, migraine and depression.17 Until now, no absolute treatment has been found for MS, therefore, trying to find a completely effective and safe treatment is still ongoing.
Use of complementary and alternative medicine (CAM), in particular herbal remedies have noticeably risen in MS patients over the last decades.18,19 Herbal therapy is known as a helpful strategy for curing the different disorders from ancient to the present time.20 Previous studies reported that medicinal plants have several therapeutic effects in different disorders such as cancers, diabetes and neurodegenerative diseases.21,22 Recently, a growing number of findings have indicated that some herbal compounds improve myelin repair and lead to suppression of inflammation.23,24 Also, there are many studies that reported the anti-inflammatory and antioxidant effects of medicinal plants, as well as other helpful properties which make them as a natural, safe and reliable remedy for treatment of neurodegenerative diseases.25,26 Perivious studies have indicated that MS patients are interested in using herbal medicines to control their disease symptoms.26 For example in China, Chinese herbal medicine (CHM) is widely used by MS patients for ameloriating the severity of disease.27 The beneficial effects of CHM in MS disease is occured by reduction of the severity of MS disease; including antioxidative properties, anti-apoptotic effects, anti-inflammatory properties and promoting the differentiation of local stem cells to myelin producing cells.28 MS patients usually use CAM, and medicinal plants as a member of this family plays a crucial role to cure MS and itsʼ associated symptoms.29 Different herbal medicines are recommended for MS patients, but the understanding of their efficacy is not well described. In this review; we will discuss some of herbal compounds beneficial effects on MS disease (Table 1 and Table 2). We conducted a search for all English language articles in Google Scholar, Science Direct, Scopus, PubMed and Medline for medicinal plants, that have been used for their therapeutic potentials in MS disease, studies which their publication dates from January 1960 to April 2018 were used.
Table 1: Summary of herbal medicines used in the treatment of Multiple sclerosis
| Plant | Author (Country) | Design of study | Dosage | Number | Duration of study | Effects | Ref |
| Ginkgo biloba | Johnson et al (USA) | Clinical trial-Double-blind, placeo-controlled | 240 mg/day of ginkgo extract | 22 MS patients | 4 weeks | Treatment with ginkgo extract relieved fatigue with no adverse effect in MS patients | 34 |
| Lovera et al (USA) | Clinical trial-Double-blind, placeo-controlled | 240 mg/day of ginkgo extract | 38 MS patients | 12 weeks | Improvement of the cognitive performance were reported in treated group | 37 | |
| Brochet et al (France) | Clinical trial-Double-blind, placeo-controlled | 240 and 360 mg/day of ginkgolide B | 104 MS patients | 1 week | ginkgolide B was not an effective treatment for exacerbations of MS | 180 | |
| Zingiberofficinale | Jafarzadeh et al (Iran) | EAE model of MS in mice | 200 and 300 mg/kg ginger extract | 24 | 4 weeks | Ginger extract ameliorated EAE severity and modulated the expression of IL-27, IL-33 | 43 |
| Curcuma longa | Xie et al (Japan) | EAE model of MS in rats | 100 and200 mg/kg curcumin extract | 21 | 2 weeks | Curcumin decreased the inflammation and the severity of EAE | 53 |
| Natarajan and Bright (USA) | EAE model of MS in SJL/J mice | 50 and 100 µg curcumin in 25 µl DMSO / day | – | 4 weeks | Curcumin decreased CNS inflammation and demyelination also,decreased the severity of EAE | 54 | |
| Mohajeri et al (Iran) | EAE model of MS in rats | 12.5 mg/kg of curcumin | 20 | 17 days | Treatment with polymerized nano-curcumin decreased the severity of EAE and increased the remyelination | 23 | |
| Oenotherabiennis | Firouzi et al (Iran) | Double blind, randomized clinical trial | 18–21 g/day Evening primrose oil and C. sativa oils | 100 MS patients | 24 weeks | Treatment with co-supplemented C. sativa and evening primrose oils decreased the clinical score in MS patients | 158 |
| Horrobin (Canada) | Double blind, randomized clinical trial | – | 14 MS patients | 24 weeks | Treatment with colchicine and evening primrose oil improved manual dexterity test and clinical score in MS patients | 159 | |
| Hypericumperforatum | Naziroglu et al (Turkey) | In-vitro study on neutrophils of MS patients | 20 μM/ml H. perforatum for 2 hours | 9 MS patients | – | Treatment with H. perforatum indicated the protective effects on oxidative stress in MS patients | 69 |
| Vacciniummacrocarpon | Gallien et al (France) | Double blind, clinical trial, placebo-controlled | 36 mg/day Cranberry extract(proanthocyanidins) | 171 MS patients | 1 year | Treatment with cranberry extract versus placebo did not prevent UTI occurrence in MS patients | 81 |
| Nigella sativa | Fahmy et al (Egypt) | EAE model of MS in rats | 2.8 g/kg Nigella sativa extract | 22 | 4 weeks | N. sativa ameliorated the clinical signs of EAE, suppressed inflammation and enhanced remyelination in the CNS | 85 |
| Noor et al (Egypt) | EAE model of MS in rats | 2.8 g/kg Nigella sativa extract | 22 | 4 weeks | N. sativa suppressed inflammation in EAE rats. Also, N sativa enhanced remyelination in the cerebellum and reduced the expression of TGF β1 | 87 | |
| Crocus sativus | Ghaffari et al (Iran) | EAE model of MS in rats | Intrahippocampal (5and 10 μg/rat) injection of the saffron | 35 | 3 days | Local injection of saffron extract modulated the oxidative stress markers (reduced the activity of GPx and SOD enzymes), through scavenging of ROS | 103 |
| Ghazavi et al (Iran) | EAE model of MS in C57bl/6 mice | 100 µL saffron extract | 20 | 3 weeks | Treatment with saffron decreased inflammation in the spinal cord and decreased the severity of EAE | 102 | |
| Panax ginseng | Hwang et al (Korea) | EAE model of MS in C57bl/6 mice | 200 μg of an acidic polysaccharide of Panax ginseng | – | 33 days | Acidic polysaccharide of Panax ginseng decreased the infiltration of inflammatory cells in the CNS, also suppressed EAE score by inhibiting the proliferation of T cells and the production of inflammatory cytokines | 113 |
| Etemadifar et al (Iran) | Randomized Double-blind, placeo-controlled | 250 mg ginseng tablets | 52 MS patients | 12 weeks | Ginseng treatment had no adverse effect on MS patients as well as reduced fatigue and had a positive effect on quality of life | 114 | |
| Boswelliapapyrifera | Sedighi et al (Iran) | Randomized, double-blinded, placebo-controlled study | 600 mg of B. papyrifera | 80 MS patients | 8 weeks | B. papyrifera improved the visuospatial memory of MS patients | 124 |
| Vitisvinifera | Sato et al (USA) | EAE model of MS in C57bl/6 mice | 20 mg/kg per day | – | 8 weeks | Resveratrol treatment worsened the demyelination and inflammation without neuroprotective effects in the CNS | 129 |
| Kelly et al (USA) | EAE model of MS in C57bl/6 mice | 100 and 250 mg/kg Sigma resveratrol | – | 4 weeks | Resveratrol delayed the onset of EAE and had a significant neuroprotective effect as well as prevents neuronal loss | 130 | |
| Shindler et al (USA) | EAE model of MS in SJL/J mice | 500 and 1000 mg/kg resveratrol | 62 | 4 weeks | Resveratrol treatment prevented neuronal loss during optic neuritis and reduced neurological dysfunction during EAE | 131 | |
| Camellia sinensis | Mahler et al (Germany) | Randomized, double-blinded, placebo-controlled study | 600 mg/d EGCG | 18 MS patients | 12 weeks | Treatment with EGCG improved muscle metabolism during moderate exercise in MS patients | 155 |
| MS14 | Tafreshi et al (Iran) | EAE model of MS in C57bl/6 mice | MS14 containing 30% of the diet | 14 | 20 days | Treatment with MS14 ameliorated the clinical signs of EAE and reduced neuropathological changes | 163 |
| Kalan et al (Iran) | EAE model of MS in C57bl/6 mice | MS14 containing 30% of the diet | 25 | 35 days | MS14 decreased EAE symptoms and lymphocyte infiltration into the CNS | 164 | |
| Kalan et al (Iran) | EAE model of MS in C57bl/6 mice | MS14 containing 30% of the diet | 25 | 35 days | Treatment with MS14 reduced clinical signs of EAE, demyelination and IL-6 production | 165 | |
| Cannabis sativa | Zajicek et al (UK) | Randomized, placebo-controlled trial | Capsules containing 2.5 mg of THC and 1.25 mg of cannabidiol | 630 MS patients | 15 weeks | cannabinoids improved patients’ mobility and improved in spasticity | 173 |
| Zajicek et al (UK) | Double blind, placebo controlled, phase III study | Capsules containing cannabidiol 0.8–1.8 mg and 2.5 mg THC | 279 MS patients | 12 weeks | Treatment with cannabinoids improved the relief from muscle stiffness in MS patients | 172 | |
| Wade et al (UK) | Double-blind, randomized, placebo-controlled study | 120 mg cannabidiol and 120 mg THC | 160 MS patients | 10 weeks | Treatment with cannabinoids improved patient’s spasticity, without any adverse effects | 174 | |
| Greenberg et al (USA) | Double-blind, randomized, placebo-controlled study | Smoking one marijuana cigarette containing 1.54% THC | 10 MS patients | 3 days | Smoking marijuana improved eyes-open and eyes-closed tests, and noise variance values | 178 | |
| Brady et al (USA) | Open-label, pilot study | 2.5 mg of THC and 2.5 mgCBD per spray | 10 MS patients | 8 weeks | Cannabinoids decreased urinaryurgency, number and volume of incontinence episodes, frequency and nocturia in MS patients.Also, spasticity and quality of sleep improved significantly in the treated group | 179 |
Table 2: Use of herbal medicines in Multiple sclerosis, according to the symptomatic problems
| Usage | Plant | References |
| Antidepressant | Hypericum perforatumCrocus sativus | 69,101 |
| Sleeping problem | Piper methysticumValeriana officinalis | 73,93 |
| Improvement in cognitive impairment | Ginkgo bilobaBoswellia papyrifera | 36,124 |
| Urinary system dysfunction | Vaccinium macrocarponCannabis sativa | 79,179 |
| Fatigue | Ginkgo bilobaPanax ginseng | 114,34 |
| Anti-inflammatory and neuroprotective | Ginkgo bilobaZingiber officinaleCurcuma longaOenothera biennisNigella sativaCrocus sativusPanax ginsengBoswellia papyriferaVitis viniferaGastrodia elataCamellia sinensisCannabis sativaMS14 | 33,34,87,101,113,124,130,140,134,159,164,167 |
Ginkgo biloba
Ginkgo biloba L. (well-known as ginkgo), is one of the oldest living tree species from the family Ginkgoaceae. Ginkgo is native to Korea and China, but now it can be found all over the world.30 Ginkgo refers to an extract of the leaves of the G. biloba trees, which traditionally used as a remedy to improve the mental alertness and memory.31 The current reputation of G. biloba can be attributed to a pioneeering research that informed G. biloba is an effective cure for cognitive issues.32
Studies have shown that anti-inflammatory and inhibiting the platelet-activating factor (PAF) properties of ginkgo extract (EGB761) are effective on MS disease.33,34 Ginkgolides is the major component of G. biloba, its effect on the PAF activity represents the possible therapeutic role of this plant on MS.34 PAF’s role in inflammation process is obviously introduced, so ginkgo can inhibit this process.35 In addition, ginkgo reverses cognitive impairment and reduces fatigue in MS patients.36,37G. biloba is generally safe with no side or adverse effects38 but in some few cases, dizziness, headaches and ocular bleeding associated with its usage.30 Consumption of G. biloba is almost safe and has obvious therapeutic effects for MS patients; improving functional status (fatigue) of people with MS and neuroprotective activities are the valuable medical properties of G. biloba.
Zingiber officinale
Zingiber officinale Roscoe (Ginger), is an aromatic plant in the family Zingiberaceae. Z. officinale is native to India and commonly grown in Asia, tropical Africa and Latin America.38 Ginger root is routinely used as an aromatic spice and a traditional drug.39 Recent studies acknowledged the anti-cancer,40 antioxidant41 and anti-inflammatory activities of ginger.42
Anti-inflammatory capacity of ginger is the reason of its consumption by MS patients.43 Gingerols and its dehydrated derivatives (shogaols), are the major components of the ginger that exhibit anti-inflammatory effects.44 The anti-inflammatory effects of 6-shogaol were reported by inhibiting the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase- 2 (COX-2) in macrophages, as well as preventing dopamine reduction and reducing apoptose rate in CNS.45 10-gingerol is another important component of ginger which attribituted with anti-inflammatory effect in fresh ginger.46 10-gingerols inhibits LPS-induced NO and production of pro-inflammatory cytokines by inhibiting the NF-jB activation.46 Positive effects of ginger and itsʼ active compounds (6-shogaol and 10-gingerol) were approved in animal models of MS, by exerting anti-inflammatory and neuroprotective effects, but still clinical studies on MS patients are needed to confirm these results.
Curcuma longa
Curcuma longa L. is a tropical plant, native to southern and southeastern tropical Asia.47 C. longa is belonging to the ginger family, Zingiberaceae. A yellow coloring-matter obtained from the roots of C. longa, is named curcumin.47 Curcumin is widely used as a dietary spice and pigment. Curcumin is commonly consumed as an Asian folk remedy for treating biliary disorders, anorexia, cough, sinusitis and sore throat.48 Studies indicated that curcumin exerts a wide range of biological activities, including anti-inflammatory,49 antitumor50 and antioxidants effects.51
Anti-inflammatory effect of curcumin has been obviously examined in different studies.44,52 Curcumin does its anti-inflammatory role in two major ways: (1) inhibition of pro-inflammatory cytokines and (2) inhibition of Th17 differentiation and its related pathways.52 Curcumin ameloriated the severity of experimental autoimmune encephalomyelitis (EAE), as a animal model of MS disease, also reduced the infiltration of inflammatory cells to the CNS.52 Curcumin modulates inflammatory process by decreasing the expression of the different pro-inflammatory and inflammatory cytokines.44,53 In one study, polymerized form of nano-curcumin was used for treating EAE model of MS, which demonstrated anti-inflammatory and antioxidative effects as well as increasing remyelination and decreasing EAE score.23 Furthermore, curcumin can decrease the secerity of MS disease by blocking IL-12 signaling pathway in T cells.54 Side effects of curcumin is associated with high dose consumption which causes nausea and diarrhea.55 Although, therapeutic effects of curcumin were demonstrated in different studies but human studies are certainly needed to confirm the recommendation of curcumin in MS patients.
Hypericum perforatum
Hypericum perforatum L. better known as St John’s Wort is a flowering plant from the family Hypericaceae. H. perforatum is a native plant in Europe and Asia but today has worldwide spread.30 From the ancient time, H. perforatum was popular plant because it had a wide range of therapeutic effects for different diseases such as anxiety, depression and menstrual disorders.56 Currently, H. perforatum is used for treating the inflammation-related disorders,57 cancers58 and neurodegenerative diseases.59
The usage of H. perforatum in MS disease is related to its antidepressant effects.60,61 Hypericin is the main antidepressant component of H. perforatum which stimulates capillary blood flow in brain.62 Studies have showed that Hypericin strongly inhibits the MAO enzymes and has a strong affinity for Sigma receptors which regulate dopamine level.63 Recent studies have shown that hypericin acts as an antagonist for adenosine, benzodiazepine and GABA receptors.64 Many studies emphasis on another constituent, Hyperforin, for the therapeutic effects of this plant. It has been reported that Hyperforin has antidepressant effects as a result of inhibiting the uptake of dopamine, serotonin, noradrenaline, GABA, and L-glutamate.65,66 There are some clinical studies which have shown the effectiveness of H. perforatum on depression conditions.60,67,68 H. perforatum can be recommended to MS patients due to its antidepressant, antioxidative and anti-inflammatory effects.69
Valeriana officinalis
Valeriana officinalis L. (Valerian) is native to Europe, North America and parts of Asia.68 Valerian is a plant in the family of Caprifoliaceae, the root and rhizome of this herb are used for different medicinal purposes.68 In ancient Greek, valerian had various medicinal applications, for example, for digestive problems, epilepsy and urinary tract infections.70 In addition, valerian was introduced as a treatment for sleeping problems and insomnia.71
Sleep disturbance is the most important cause of fatigue in MS patients.72 Clinical trials demonstrated that major component of V. officinalis root extract, valerenic acid, is effective in treatment of mild-to-moderate sleeping disorders.73 Like benzodiazepines which are GABA-analogs, valerenic acid has particular affinity for the GABAA receptor.30 Limited adverse effects such as stomachache and allergic reaction have been observed in patients under treatment of valerenic acids.30,74 Consumption of V. officinalis can be suggested to MS patients due to the ameliorating effects on sleeping problems and fatigue status.
Vaccinium macrocarpon
Vaccinium macrocarpon (Cranberry, Large Cranberry), is a North American species of cranberry in Ericaceae family. Cranberry juice is obtained from the V. macrocarpon fruit.75 Cranberry has been traditionally used for treatment of bladder and kidney disorders by Native Americans.75,76
MS patients are susceptible to the urinary tract colonizations (UTC) and urinary tract infections (UTIs), as a result of the bladder dysfunction in MS disease.77 Studies have shown that cranberry juice or its produced-capsules is a beneficial remedy for treatment of UTIs.78 It has been reported that cranberry can inhibit Escherischia coli adherence to the urethra.79 Cranberry has two substantial compounds, fructose and proanthocyanidin, that stick to the fimbriae of E. coli and effectively hindering the bacteriaʼs ability to attach to the urethra.79 There are a few clinical studies that examined the preventive effects of cranberry on UTIs in MS patients.80 However, in different studies cranberry was found to be effective against urinary tract infections, but in one clinical trial of MS patients, it not showed acceptable prevention from urinary tract infections.81
Nigella sativa
Nigella sativa L. usually known as black seed is widely used as a medicinal plant belongs to the family Ranunculaceae. Black seed is native to Southern Europe, Southwest Asia and North Africa.82 Seeds and oil of N. sativa has a long historical and religious background for treatment of various illnesses such as headache, back pain and gastrointestinal problems.83,84 Several studies have shown that black seed has diverse therapeutic effects, including anticancer, analgesic, antimicrobial, anti-inflammatory, renal protective and antioxidant properties.84,85 Thymoquinone is the active compound of N. sativa seeds.86
There are several evidences that indicated the anti-inflammatory capacity of black seed oil.85,87 In vitro studies demonstrated the inhibitory effects of N. sativa oil and its active compound, thymoquinone, on the production of inflammatory mediators {such as IL-1b, IL-6, TNF-a, IFN-c and PGE2}.88,89 In addition, Black seed oil inhibited COX and 5-LO pathways of arachidonate metabolism.89,90 Thymoquinone also potently inhibiting the non-enzymatic peroxidation in brain phospholipid liposomes.84 The therapeutic effects of N. sativa in animal models of MS were reported. N. sativa enhanced remyelination in CNS, reduced inflammation processes and suppressed the expression of TGF β1 in EAE models of MS disease.87
Piper methysticum
Piper methysticum (kava kava) is a psychoactive herb in the family Piperaceace, which has been used in the Pacific Islands for hundreds of years. The root of this plant is well-known for its sedative and anesthetic properties.80 Kava traditionally used for producing a comforting and relaxing drink.80,91
Combination of kava and valerian seems to be more effective for treatment of stress-induced insomnia than either herb alone.92 The active compound of kava is cavalactones, which interacts with GABAA receptors and decreases anxiety and sleeping problems.93,94 Kava also can potentiate the sedating effects of the drugs that usually used in MS disease such as Lioresal (Baclofen).95 Extensive use of kava may lead to hepatotoxicity, hepatic necrosis and cholestasis hepatitis.96 It can be concluded that kava alone or in combination with other herbal medicines is a promising candidate for treating anxiety disorders of MS patients.
Crocus sativus
Crocus sativus L. (Saffron) is a flowering plant in the family Iridaceae. Saffron stigma has been widely used as a medicinal plant for healing the different disorders.97 Saffron has been commonly used as an herbal drug for its sedative, stimulant and anticatarrhal properities.97,98 Several studies suggested that saffron can be effective in treatment of hypertension and memory impairments. Additionally, saffron has been demonstrated anti-inflammatory and antitussive effects.99 Crocetin and crocin are the two main active compounds of saffron stigma, which have a wide range of therapeutic activitis.100
Antidepressant and anti-neuroinflammatory effects of saffron are evidently effective in MS disease.101–103 Crocin exerts its anti-inflammatory effects via inhibiting syncytin-1 and nitric oxide (NO)-induced astrocyte and oligodendrocyte cytotoxicity, also decreases neurological injuries in experimental autoimmune encephalomyelitis (EAE).104,105 Syncytin-1 is highly expresses in microglia, astrocytes and glial cell of MS lesions.106 Studies have shown that crocin has antidepressant effects in mild to moderate depression.99 Excessive consumption of saffron induces dizziness, nausea, vomiting and diarrhea.107 Depression is a common condition in MS disease which adversely affect health status. According to this point, antidepressant activity of saffron can be highly helpful in depressive disorders of MS patients.
Panax ginseng
Panax ginseng also known as Asian ginseng is a traditional herbal medicine in Asia for thousands of years, which belongs to the Araliaceae family.108 Ginseng root is traditionally used in powdered form to regenerate the body and mind, increase physical strength and prevent aging.109 The main active compound of P. ginseng is ginsenosides, that exhibits anti-inflammatory, antioxidant, and anti-apoptotic properties.110,111In addition, P. ginseng is one of the most useful medicinal plants for curing different neuroinflammatory diseases such as Parkinson’s disease, Alzheimer’s disease, Huntington’s disease and Multiple sclerosis.112
Some evidences have indicated that ginseng can decrease the inflammation and fatigue, which may be useful in MS patients.113,114 Ginseng reduced the severity of EAE by inhibiting the proliferation of T cells, inhibiting the production of the inflammatory cytokines (FN-γ, IL-1β and IL-17) and depleting of CD25+ cells.113 In clinical studies ginseng led to fatigue improvement and had a positive effect on quality of life.114 Excessive intake of ginseng can lead to several adverse effects including hypertension, insomnia, rashes and diarrhea.115 We can deduce that ginseng is an effective remedy for curing MS-related fatigue and enhancing quality of life in these patients.
Boswellia papyrifera
Boswellia papyrifera belongs to the Burseraceae family.116 Gum production through resin of B. papyrifera, has high economic value.117 The resin of B. papyrifera has been traditionally used in treatment of ulcers, chronic inflammation and for memory support.118 The main active compound of B. papyrifera resin is boswellic acids.119 Several studies have indicated the different therapeutic effects of boswellic acids such as anti-inflammatory, antitumor and antioxidant effects.120,121
Cognitive impairment is a common clinical symptom in MS patients, with incidence rates up to 70%.122 Cognitive deficits in MS patients affect various aspects including attention, information processing efficiency, processing speed, long term memory and visual learning.123 Anti-inflammatory and neuroprotective properties of B. papyrifera, reversed the cognitive impairments in MS patients.124 In one clinical trial, patients with MS which received B. papyrifera, had a significant visuospatial memory improvement compared to the control group.124 Administration of B. papyrifera enhances cognitive impairment in MS patients, but still there is a need for large scale trials to completely clarify the therapeutic effects of B. papyrifera in MS patients.
Vitis vinifera
Vitis vinifera L. (common grape vine) is one of the most important fruit crops in the world from the family Vitaceae. V. vinifera is cultivated in the most countries of Europe, Northern Africa and Western Asia.125 The leaves and seeds of this plant have various medicinal properties. Resveratrol (trans-3, 4, 5-trihydroxystilbene) is a phenolic compound that produced in the grapes in response to injuries of fungal pathogens.126 Resveratrol has been reported to have several pharmaceutical effects such as anti-inflammatory, anticancer, antioxidant and antiviral properties.127,128
Both neuroprotective and anti-inflammatory effects of resveratrol were informed in several researches.129–131 Resveratrol exhibits neuroprotective effects by inhibiting the microglia activation and decreasing the pro-inflammatory factors production through the MAPKs, phosphoinositide3-kinase (PI3-K)/Akt, glycogen synthase kinase-3β (GSK-3β) and NADPH oxidase signaling pathway.127,132,133 Resveratrol can cross the blood–brain barrier (BBB), therefore it can be an ideal candidate for treating neuroinflammatory and neurodegenerative diseases.129,134 Excessive intake of common grape causes gastrointestinal side effects including nausea, abdominal pain, flatulence and diarrhea.135 Neuroprotective effects of V. vinifera were demonstrated in different neurodegenerative diseases, but more specific studies on MS disease are needed to determine itʼs therapeutic role in MS.
Gastrodia elata
Gastrodia elata Blume (tianma) is a saprophytic herb from the family Orchidaceae. G. elata is a traditional Chinese plant, native to the oriental countries.136 Tianma is the dried rhizome of the G. elata which were used as a traditional herbal medicine for a variety of conditions such as headaches, vertigo and hypertension.137 In addition, tianma is commonly used for the treatment of neurodegenerative disorders and memory improvement.138,139
Due to neuroprotective and anti-neuroinflammatory effects of G. elata, it can be considered as a promising candidate for MS therapy. G. elata reduces oxygen free radicals and protects against neuronal damage.137,140,141 G. elata indicated anxiolytic-like properties via the GABA-ergic nervous system.142 It has been reported that G. elata has protective effects against global ischemia, nitric oxide synthase activity and apoptosis.143 Gastrodin is the main active component of the tianma which mediates its neuroprotective effects.144 Vanillin and Benzyl alcohol are the other active compouds of G. elata that have anti-inflammatory effects by inhibiting the generation of reactive oxygen species (ROS) and inhibiting the activities of cyclooxygenase- (COX-) 1 and COX-2.145G. elata plays an important protective role in the neurorestorative processes, therefore it can be a helpful remedy for MS patients. however, future animal models and clinical studies of MS disease are needed to clarify the possible therapeutic effects of this plant on MS patients.
Camellia sinensis
Camellia sinensis L. is well known as green tea, one of the oldest beverages in the world from the Theaceae family.146,147 Dried leaves of C. sinensis are used in green tea production.147 Green tea is used for several different purposes including weight loss, cardiovascular disorders, inflammation and neuroprotective effects.148
Green tea exhibits anti-inflammatory and neuroprotective properties.149,150 Epigallocatechin-3-gallate (EGCG) is one of the most important active compounds of green tea which is attributed to anti-inflammatory and neuroprotective properties of this plant.134 EGCG is a polyphenol compound that inhibits the production of inflammatory mediators such as TNF-α, IL-1β and IL-6 and improvs the neuroprotection in nervous system.151,152 In other studies, EGCG inhibited LPS-induced microglial activation and protected against inflammation-mediated dopaminergic neuronal injury.153 Regular and habitual consumption of green tea is safe, but, consuming high doses causes liver toxicity.154 Green tea has anti-inflammatory effects which can protect CNS from neurodegenerative diseases such as MS. Also, green tea regulates energy expenditure in the body which may relief MS-related fatigue.155
Oenothera biennis
Oenothera biennis L. (Evening primrose) is a species in the family of Onagraceae. Evening primrose oil is produced from the seeds of O. biennis which has numerous pharmacological effects.156 The traditional consumptions of this plant was for the treatment of swelling in the body, then were used for other problems such as skin disorders, gastro-intestinal disorders and asthma.157 Two parts of the plant; flowers and seeds, are used for extracting the oils.
The application of Evening primrose oil in treatment of MS is related to its anti-inflammatory and immune-modulating effects.158,159 These beneficial effects largely related to the evening primrose oil abundant supply of polyunsaturated fatty acids (PUFA) content.159 Gamma-linolenic acid is a precursor of prostaglandin and it is responsible for anti-inflammatory effects of evening primrose oil.158 In clinical trials, Evening primrose oil led to significant performance improvement in the manual dexterity test.159 In another clinical study gamma-linolenic acid rich oil had an obvious effect in relapsing-remitting MS, which meaningfully decreased the relapse rate and the progression of disease.160 However, more clinical trials are needed to prove the therapeutic effects of Evening primrose oil in MS patients.
MS14 (Penaeus latisculatus, Apium graveolens and Hypericum perforatum)
MS14 is an Iranian natural herbal-marine drug, which has obvious therapeutic effects on MS patients.161,162 MS14 consists of 90% Penaeus latisculatus, 5% Apium graveolens and 5% Hypericum perforatum.163 In both animal models and human clinical trials, MS14 was effective in treatment of MS.162,164 Antioxidant and anti-inflammatory effects, are the two features of MS14 that halt the progression of MS disease.161 MS14 showed some benefits on quality of life and improvement of patients’ mobility (lower limb).162 The neuroprotective and anti-inflammatory properties of MS14 were reported by suppressing the proliferation responses of T cells and decreasing the expression levels of IL-6, IL-5, IL-10, TNF-α and IL-1β. Furthermore, MS14 inhibited the inflammatory cell infiltration into the CNS and up-regulated LCN2 in all stages of EAE.164,165 Oral consumption of MS14 was reported properly safe without any adverse effects.162 MS14 is an herbal-marine drug that has beneficial effects in MS disease and other neroudegenerative disorders, but still more studies are needed to find various mechanisms and pathways that MS14 shows itʼs neuroprotective effects.
Cannabis sativa
Cannabis sativa L. (Bang, Marijuana, and Hachis) is a flowering plant in the genus Cannabis from the Cannabaceae family. C. sativa is native to Western and Central Asia, but extensively cultivated in Asia and Europe.166C. sativa has traditionally been used for healing the different diorders such as allergies, inflammation and sexually transmitted diseases.167 Seeds, leaves and flowers of C. sativa was reported to have various therapeutic and medicinal values. There are numerous studies that indicated the pharmacological usage of C. sativa, including analgesic effect, anticancer activity, anti-inflammatory activity, central nervous system depressant activity and immunomodulatory effect.166
C. sativa is the most important and the most common plant which is using for treating of MS. There are numerous studies that indicated cannabinoids consumption reduced muscle stiffness, bladder disturbance, spasms, neuropathic pain and sleep disorders in MS patients.168,169 The major compound of C. sativa is ∆-9tetrahydrocannabinol (THC).170 THC binds to cannabinoid receptors (CBR) in the CNS and acts as a partial agonist to CB1 and CB2 receptors.171 THC was shown to have anti-inflammatory and neuroprotective properties.167 Some studies have shown the applications of cannabinoids for improvments of spasticity in MS, consumption of cannabinoids led to significant improvement in patient-reported spasticity.172–174 Also, the combination of THC and cannabidiol (CBD) was more effective for treatment of moderate to severe refractory spasticity in MS patients.175 Cannabinoids and their synthetic drugs indicated attractive anti-inflammatory effects in animal models of MS.176 Synthetic cannabinoids can reduce inflammation by suppressing the TNF-α production in the brain. Also, Synthetic cannabinoids can improve motor function by preventing the infiltration of immune cells into the CNS, and can decrease the pro-inflammatory cytokines secretion such as IFN-µ, IL-17, IL-6, IL-1β and TNF-α.167 Sativex is a combination of the two derived cannabinoids of the C. sativa; THC and CBD, which has been formulated for oromucosal mouth spray to relief neuropathic pain, spasticity, sleeping difficulties, bladder disturbance and other symptoms associated with MS.177 Orally administration of THC can decrease the intensity of several signs and symptoms of MS such as, decreasing spasticity, rigidity, tremor, as well as improving walking ability, performance of handwriting and bladder control.169 Smoking marijuana in patients with MS demonstrated to have some advantageous effects, including healing the spasticity, pain, tremor and emotional dysfunction.178 In one clinical trial, cannabinoids decreased the urinary symptoms, urinary incontinence, frequency of urination and nocturia in treated group.179 There are some adverse effects associated with C. sativa such as the risks of cancer, cardiovascular disease, nausea, vomiting and impaired driving.61
Conclusion
Medicinal plants have opened a new horizon in curing neurodegenerative disorders such as Parkinson’s disease, AD and MS. literature data review indicated that herbal medicines could be effective in the treatment of MS disease and itsʼ related symptoms, by reducing the demyelination, improving remyelination and suppressing the inflammation in the CNS. On the basis of the above mentioned review, it can be concluded that the anti-inflammatory effect is the main reason of medicinal plants therapeutic effects in MS disease, through which medicinal plants ameliorate the severity of disease and reduce neuropathological changes. Anti-inflammatory effects of medicinal plants usually occur through inhibiting the inflammatory cell infiltration into the CNS, decreasing the production of pro-inflammatory and inflammatory cytokines. Further studies are needed to disclose the exact mechanisms of action, through which medicinal plants exhibit their anti-inflammatory and neuroprotective effects. Given that most studies of herbal therapy effects in MS have been done on animal models, still there is a great need for approving these studies by clinical trials to recommend these mentioned plants for MS patients. In addition to neuroprotective effect, medicinal plants have other beneficial effects for MS patients, such as sedation, improving sleep quality, anti-depressant effects, relief muscle stiffness and reducing bladder disturbance.
Ethical Issues
Not applicable.
Conflicts of Interest
All authors declare no conflicts of interest.
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