Neuroprotective potential of Celastrus paniculatus seeds against common neurological ailments: a narrative review
Abstract
The most common human neurodegenerative diseases like Alzheimer’s disease (AD), Parkinson’s disease (PD), Huntington’s disease (HD) etc. have been recognized to result from a complex interplay between genetic predisposition and defective cellular dynamics such as inappropriate accumulation of unfolded proteins, oxygen free radicals and mitochondrial dysfunction. The treatment strategies available today for these neurodegenerative ailments are only palliative and are incapable of restraining the progression of the disease. Hence, there is an immense requirement for identification of drug candidates with the ability to alleviate neuronal damage along with controlling progression of the disease. From time immemorial mankind has been relying on plants for treating varied types of dreadful diseases. Among the various medicinal plants used for treating various neurological ailments, Celastrus paniculatus (CP) popularly known as Jyotishmati or Malkangni is well known in the Ayurveda system of Indian Traditional Medicine whose seeds and seed oil have been used for centuries in treating epilepsy, dementia, facial paralysis, amnesia, anxiety, sciatica, cognitive dysfunctions etc. This review apart from specifying the phytochemical characteristics and traditional uses of C. paniculatus seeds and seed oil also exemplify the comprehensive data derived from various research reports on their therapeutic potential against some common neurological disorders.
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Research funding: No funding has been involved.
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Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission. All authors have contributed equally to the conception of topic, interpretation and correlation of available literature evidence for the preparation of this review article.
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Competing interests: All authors manifest that there are no conflict of interests.
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Informed consent: Not applicable.
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Ethical approval: Not applicable (no human participants, human data or human tissue involved).
References
1. Gitler, AD, Dhillon, P, Shorter, J. Neurodegenerative disease: models, mechanisms, and a new hope. Dis Model Mech 2017;10:499. https://doi.org/10.1242/dmm.030205.Suche in Google Scholar PubMed PubMed Central
2. Bertram, L, Tanzi, RE. The genetic epidemiology of neurodegenerative disease. J Clin Invest 2005;115:1449. https://doi.org/10.1172/jci24761.Suche in Google Scholar PubMed PubMed Central
3. Brown, RC, Lockwood, AH, Sonawane, BR. Neurodegenerative diseases: an overview of environmental risk factors. Environ Health Perspect 2005;113:1250. https://doi.org/10.1289/ehp.7567.Suche in Google Scholar PubMed PubMed Central
4. Hussain, R, Zubair, H, Pursell, S, Shahab, M. Neurodegenerative diseases: regenerative mechanisms and novel therapeutic approaches. Brain Sci 2018;8:177. https://doi.org/10.3390/brainsci8090177.Suche in Google Scholar PubMed PubMed Central
5. Sweeney, P, Park, H, Baumann, M, Dunlop, J, Frydman, J, Kopito, R, et al.. Protein misfolding in neurodegenerative diseases: implications and strategies. Transl Neurodegener 2017;6:6. https://doi.org/10.1186/s40035-017-0077-5.Suche in Google Scholar PubMed PubMed Central
6. Alok, S, Jain, SK, Verma, A, Kumar, M, Sabharwal, M. Pathophysiology of kidney, gallbladder and urinary stones treatment with herbal and allopathic medicine: a review. Asian Pac J Trop Dis 2013;3:496–504. https://doi.org/10.1016/s2222-1808(13)60107-3.Suche in Google Scholar
7. Athira, K, Sajeev, CR, Saroj, KV, Sooraj, NP, Sunil Kumar, KN, Jaishanker, R. Mapping traditional knowledge associated with Celastrus paniculatus in India using geographical information system (GIS). J Ayurveda Med Sci 2017;1:55–62.10.5530/jams.2016.1.9Suche in Google Scholar
8. Kulkarni, R, Girish, KJ, Kumar, A. Nootropic herbs (Medhya Rasayana) in Ayurveda: an update. Pharmacogn Rev 2012;6:147. https://doi.org/10.4103/0973-7847.99949.Suche in Google Scholar PubMed PubMed Central
9. Valecha, R, Dhingra, D. Behavioral and biochemical evidences for antidepressant-like activity of celastrus paniculatus seed oil in mice. Basic Clin Neurosci 2016;7:49–56.Suche in Google Scholar
10. Dey, A, Bhattacharya, R, Mukherjee, A, Pandey, DK. Natural products against Alzheimer’s disease: pharmaco-therapeutics and biotechnological interventions. Biotechnol Adv 2017;35:178–216. https://doi.org/10.1016/j.biotechadv.2016.12.005.Suche in Google Scholar PubMed
11. Debnath, M, Biswas, M, Shukla, V, Nishteswar, K. Phytochemical and analytical evaluation of Jyotishmati (Celastrus paniculatus Willd.) leaf extracts. AYU (An Int Q J Res Ayurveda) 2014;35:54. https://doi.org/10.4103/0974-8520.141929.Suche in Google Scholar PubMed PubMed Central
12. Ramadan, MF, Kinni, SG, Rajanna, LN, Seetharam, YN, Seshagiri, M, Mörsel, JT. Fatty acids, bioactive lipids and radical scavenging activity of Celastrus paniculatus Willd. seed oil. Sci Hortic (Amst) 2009;123:104–9. https://doi.org/10.1016/j.scienta.2009.07.008.Suche in Google Scholar
13. Dwivedi, V, Maurya, H. A comprehensive overview of Celastrus paniculatus seed oil intended for the management of human ailments. Indian J Pharmaceut Biol Res 2018;6:37–42. https://doi.org/10.30750/ijpbr.6.2.7.Suche in Google Scholar
14. Gamlath, CB, Leslie Gunatilaka, AA, Tezuka, Y, Kikuchi, T, Balasubramaniam, S. Quinone-methide, phenolic and related triterpenoids of plants of Celastraceae: further evidence for the structure of Celastranhydride. Phytochemistry 1990;29:3189–92. https://doi.org/10.1016/0031-9422(90)80182-g.Suche in Google Scholar
15. Tu, YQ, Chen, YZ, Wu, DG, Zhang, XM, Hao, XJ. Sesquiterpenoids from Celastrus paniculatus. J Nat Prod 1993;56:122–5. https://doi.org/10.1021/np50091a017.Suche in Google Scholar
16. Kulkarni, YA, Agarwal, S, Garud, MS. Effect of Jyotishmati (Celastrus paniculatus) seeds in animal models of pain and inflammation. J Ayurveda Integr Med 2015;6:82–8. https://doi.org/10.4103/0975-9476.146540.Suche in Google Scholar PubMed PubMed Central
17. Mishra, B, John, E, Joy, K, R, B, R, A. Toxicity profile of Celastrus paniculatus seeds: a preclinical study. Asian J Pharmaceut Clin Res 2020;13:115–8. https://doi.org/10.22159/ajpcr.2020.v13i7.37803.Suche in Google Scholar
18. Winkler, J, Suhr, ST, Gage, FH, Thal, LJ, Fisher, LJ. Essential role of neocortical acetylcholine in spatial memory. Nature 1995;375:484–7. https://doi.org/10.1038/375484a0.Suche in Google Scholar PubMed
19. Aisen, PS. The potential of anti-inflammatory drugs for the treatment of Alzheimer’s disease. Lancet Neurol 2002;1:279–84. https://doi.org/10.1016/s1474-4422(02)00133-3.Suche in Google Scholar PubMed
20. Kumar, MHV, Gupta, YK. Antioxidant property of Celastrus paniculatus Willd.: a possible mechanism in enhancing cognition. Phytomedicine 2002;9:302–11. https://doi.org/10.1078/0944-7113-00136.Suche in Google Scholar PubMed
21. Bhanumathy, M, Harish, MS, Shivaprasad, HN, Sushma, G. Nootropic activity of Celastrus paniculatus seed. Pharm Biol 2010;48:324–7. https://doi.org/10.3109/13880200903127391.Suche in Google Scholar PubMed
22. Nalini, K, Karanth, KS, Rao, A, Aroor, AR. Effects of Celastrus paniculatus on passive avoidance performance and biogenic amine turnover in albino rats. J Ethnopharmacol 1995;47:101–8. https://doi.org/10.1016/0378-8741(95)01264-e.Suche in Google Scholar PubMed
23. Malik, J, Karan, M, Dogra, R. Ameliorating effect of Celastrus paniculatus standardized extract and its fractions on 3-nitropropionic acid induced neuronal damage in rats: possible antioxidant mechanism. Pharm Biol 2017;55:980–90. https://doi.org/10.1080/13880209.2017.1285945.Suche in Google Scholar PubMed PubMed Central
24. Jadhav, K, Marathe, P, Rege, N, Raut, S, Parekar, R. Effect of Jyotiṣmatī seed oil on spatial and fear memory using scopolamine induced amnesia in mice. Ancient Sci Life 2015;34:130. https://doi.org/10.4103/0257-7941.157149.Suche in Google Scholar PubMed PubMed Central
25. Bhagya, V, Christofer, T, Shankaranarayana Rao, BS. Neuroprotective effect of Celastrus paniculatus on chronic stress-induced cognitive impairment. Indian J Pharmacol 2016;48:687–93. https://doi.org/10.4103/0253-7613.194853.Suche in Google Scholar PubMed PubMed Central
26. Lekha, G, Mohan, K, Samy, IA. Effect of Celastrus paniculatus seed oil (Jyothismati oil) on acute and chronic immobilization stress induced in swiss albino mice. Pharmacogn Res 2010;2:169. https://doi.org/10.4103/0974-8490.65512.Suche in Google Scholar PubMed PubMed Central
27. Chakrabarty, M, Bhat, P, Kumari, S, D’Souza, A, Bairy, KL, Chaturvedi, A, et al.. Cortico-hippocampal salvage in chronic aluminium induced neurodegeneration by Celastruspaniculatus seed oil: neurobehavioural, biochemical, histological study. J Pharmacol Pharmacother 2012;3:161–71. https://doi.org/10.4103/0976-500X.95520.Suche in Google Scholar PubMed PubMed Central
28. Sheth, UK, Vaz, A, Deliwala, CV, Bellare, RA. Behavioural and pharmacological studies of a tranquilising fraction from the oil of Celastrus paniculatus (Malkanguni Oil). Arch Int Pharmacodyn Ther 1963;144:34–50.Suche in Google Scholar
© 2022 Walter de Gruyter GmbH, Berlin/Boston
Artikel in diesem Heft
- Frontmatter
- Reviews
- The effect of lavender on mothers sleep quality in the postpartum period: a systematic review and meta-analysis
- The effect of Salvia officinalis on blood glycemic indexes and blood lipid profile in diabetic patients: a systematic review and meta-analysis
- Neuroprotective potential of Celastrus paniculatus seeds against common neurological ailments: a narrative review
- Intuitive and mindful eating to improve physiological health parameters: a short narrative review of intervention studies
- Research Articles
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- Intra-stromal injection of honey-treated keratocytes as a cell-based therapy for experimental corneal laceration
- Effect of Annona squamosa leaf extract on human promyelocytic leukemia cells subjected to oxidative stress
- Cinnamic acids as promising bioactive compounds for cancer therapy by targeting MAPK3: a computational simulation study
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- Immediate effect of a meditation technique on blood glucose, state anxiety and relaxation in patients with type 2 diabetes: a pilot randomized crossover study
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- Short Communication
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Artikel in diesem Heft
- Frontmatter
- Reviews
- The effect of lavender on mothers sleep quality in the postpartum period: a systematic review and meta-analysis
- The effect of Salvia officinalis on blood glycemic indexes and blood lipid profile in diabetic patients: a systematic review and meta-analysis
- Neuroprotective potential of Celastrus paniculatus seeds against common neurological ailments: a narrative review
- Intuitive and mindful eating to improve physiological health parameters: a short narrative review of intervention studies
- Research Articles
- Vitamin C supplementation modulates crude oil contaminated water induced gravid uterine impaired contractile mechanism and foetal outcomes in Wistar rats
- Acute and sub acute toxicity of Amirdha Gandhi Kukkil Vallathy an effective Siddha herbo mineral formulation used in the treatment of rheumatoid arthritis in wistar albino rat model
- Anti-hyperplastic effects of the Dacryodes edulis (Burseraceae) leaves aqueous extract on tamoxifen-induced endometrium hyperplasia on Wistar rat
- Vitamin A and vitamin D3 protect the visual apparatus during the development of dopamine-2 receptor knockout mouse model of Parkinsonism
- Leaf paste of Telfairia occidentalis favourably modulates deleterious effects associated with exposure to diethylnitrosamine in male Wistar rats
- Chemical composition, antioxidant, and enzyme inhibitory properties of Rauwolfia vomitoria extract
- Intra-stromal injection of honey-treated keratocytes as a cell-based therapy for experimental corneal laceration
- Effect of Annona squamosa leaf extract on human promyelocytic leukemia cells subjected to oxidative stress
- Cinnamic acids as promising bioactive compounds for cancer therapy by targeting MAPK3: a computational simulation study
- Cowanin induces apoptosis in breast cancer cells via Bcl-2 signaling pathway
- Arq Ajīb – a wonder Unani formulation for inhibiting SARS-CoV-2 spike glycoprotein and main protease – an in silico approach
- Immediate effect of a meditation technique on blood glucose, state anxiety and relaxation in patients with type 2 diabetes: a pilot randomized crossover study
- Effect of moderate intensity resistance training with blood flow restriction on muscle strength and girth in young adults – a randomized control trial
- Short Communication
- Icosapent ethyl (VASCEPA®) as treatment for post-acute sequelae of SARS CoV-2 (PASC) vaccine induced injury and infection