Abstract
Ayurveda uniquely describes health as a state of mental and spiritual well-being apart from physical well-being. It has imparted an etiology of mental origin to various diseases. The basic memory functions are regarded to be a combination of the power of acquisition (Grahana), retention (Dharana), and recollection (Smarana).
The fundamental doctrine of “Tridosha” states that Vata, Pitta, and Kapha are the three (energy) or biological rhythms regulating the physical and mental functioning of the human body. Pitta is responsible for understanding and grasping knowledge due to its Satva, Aashukari, and Tikshna property. Vata is responsible for the association of ideas. Kapha provides stability, which is necessary for the retention of memory.
The seers have stated that a drug exhibits its action either by its Rasa, Guna, Veerya, Vipaka, and Prabhava. This pentad ultimately influences the alteration in the status of Dosha. Similarly, Satva corresponding to Pitta, Raja corresponding to Vata, and Tama corresponding to Kapha are stated to regulate the functions of the brain and intellect in humans. It is the proper combination of the pentad above in medicinal plant drugs that aids in altering the deranged mechanisms of cognitive functions as per Ayurveda. Sheeta veerya, along with madhura rasa and madhura vipaka, improves retention power and katu rasa, katu vipaka, and ushna veerya drugs enhance the ability to acquire new information and data interpretation. The concept of Veerya is close to the “Yin and Yang” theory of Chinese medicine. Many medicinal plants viz. Guduchi, Yashtimadhu, Brahmi, and so on have been entitled as medhya rasayana, i.e., these are bestowed with enhanced properties to correct the cognitive dysfunction. Apart from these, various other drugs based on the pentad principle mentioned above have been said to participate in augmenting functions of different levels of brain and intellect.
Thus, it is the need of the hour to understand the rationale of Ayurveda’s ideology behind the management of cognitive dysfunctions. It will undoubtedly help researchers to understand and find leads in various disorders of the nervous system. The chapter will explore the rationale of Ayurveda in the management of cognitive disorders.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
Abbreviations
- Ach:
-
Acetylcholine
- AChE):
-
Acetylcholinesterase
- AD:
-
Alzheimer’s disease
- AS:
-
Argyreia speciosa
- BDNF:
-
Brain-derived neurotrophic factor
- BM:
-
Bacopa monnieri
- CAT:
-
Catalase
- DAD:
-
Diallyl disulfide
- DAT:
-
Diallyl trisulfide
- EPM:
-
Elevated plus-maze
- GABA:
-
Gamma aminobutyric acid
- GSH:
-
Glutathione
- LIF:
-
Leukaemia inhibitory factor
- MAO-A:
-
Monoamine oxidase A
- NO:
-
Nitric oxide
- PDE:
-
Phosphodiesterase
- PTU:
-
Propylthiouracil
- RAM:
-
Radial arm maze
- ROS:
-
Reactive oxygen species
- SOD :
-
Superoxide dismutase
- STZ:
-
Streptozotocin
- TGF-β3:
-
Transforming growth factor-beta 3
- TH-IR:
-
Tyrosine hydroxylase immunoreactive
- TNF-α:
-
Tumour necrosis factor
References
Ahirwar S, Tembhre M (2016) Assessment of acetylcholinesterase inhibition by Bacopa monneiri and acephate in hippocampus of chick brain for impediment of Alzheimer’s disease. Pharm Pharmacol Int J 4:413–417. https://doi.org/10.15406/ppij.2016.04.00088
Ahmad M, Yousuf S, Khan MB et al (2006) Attenuation by Nardostachys jatamansi of 6-hydroxydopamine-induced parkinsonism in rats: behavioral, neurochemical and immunohistochemical studies. Pharmacol Biochem Behav 83(1):150–160. https://doi.org/10.1016/j.pbb.2006.01.005
Akhtar M, Imam SS, Ahmad MA et al (2014) Neuroprotective study of Nigella sativa—loaded oral provesicular lipid formulation: in vitro and ex vivo study. Drug Deliv 21:487–494. https://doi.org/10.3109/10717544.2014.886640
Akhtar S, Ismail T, Fraternale T, Sestili P (2015) Pomegranate peel and peel extracts: chemistry and food features. Food Chem 174:417–425. https://doi.org/10.1016/j.foodchem.2014.11.035
Ambikar DB, Mohanta GP (2013) Neuroprotective effect of petroleum ether, methanolic and aqueous extracts of flower heads of Sphaeranthus indicus on lipofuscinogenesis and fluorescence product in brain of D-galactose induced aging accelerated mice. Orient Pharm Exp Med 13:301–306. https://doi.org/10.1007/s13596-013-0110-x
Asiaei F, Fazel A, Rajabzadeh AA, Hosseini M (2017) Neuroprotective effects of Nigella sativa extract upon the hippocampus in PTU-induced hypothyroidism juvenile rats: a stereological study. Metabolic Brain Dis 32:1755–1765. https://doi.org/10.1007/s11011-017-0025-1
Bhagya V, Christofer T, Rao BSS (2016) Neuroprotective effect of Celastrus paniculatus on chronic stress-induced cognitive impairment. Ind J Pharmacol 48:687–693. https://doi.org/10.4103/0253-7613.194853
Bhanumathy M, Harish MS, Shivaprasad HN, Sushma G (2010) Nootropic activity of Celastrus paniculatus seed. Pharm Biol 48:324–327. https://doi.org/10.3109/13880200903127391
Bhatt M, Kothiyal P (2015) A review article on phytochemistry and pharmacological profiles of Nardostachys jatamansi DC- medicinal herb. J Pharmacog Phytochem 3(5):102–106
Bihaqi SW, Sharma M, Singh AP, Tiwari M (2009) Neuroprotective role of Convolvulus pluricaulis on aluminum induced neurotoxicity in rat brain. J Ethnopharmacol 124:409–415. https://doi.org/10.1016/j.jep.2009.05.038
Chakkaravarthi N (2015) Neuroprotective effect of hydro-alcoholic extract of Boerhaavia diffusa Linn against MPTP-induced neurodegeneration in rats. Dissertation submitted in partial fulfillment of the Master of Pharmacy in Pharmacology. http://repository-tnmgrmu.ac.in/id/eprint/4938
Chang CL, Lin CS (2012) Phytochemical composition, antioxidant activity, and neuroprotective effect of Terminalia chebula Retzius extracts. Evid Based Complement Alternat Med:125247. https://doi.org/10.1155/2012/125247
Chauhan PS, Satti NK, Suri KA, Amina M, Bani S (2010) Stimulatory effects of Cuminum cyminum and flavonoid glycoside on cyclosporine-a and restraint stress induced immune-suppression in Swiss albino mice. Chem Biol Interact 185(1):66–72. https://doi.org/10.1016/j.cbi.2010.02.016
Chiroma SM, Hidayat Baharuldin MT, Mat Taib CN et al (2019) Protective effect of Centella asiatica against D-galactose and aluminium chloride induced rats: behavioral and ultrastructural approaches. Biomed Pharmacother 109:853–864. https://doi.org/10.1016/j.biopha.2018.10.111
Chunekar KC, Pandey GS (2018) Bhavaprakashnighantu. Reprint, Chaukhambha Krishnadas Academy, Varanasi, p 439
Desai SK, Desai SM, Navdeep S et al (2011) Antistress activity of Boerhaavia diffusa root extract and a polyherbal formulation containing Boerhaavia diffusa using cold restraint stress model. Int J Pharm Pharmaceut Sci 3(1):130–132
Dhingra D, Joshi P (2012) Antidepressant-like activity of Benincasa hispida fruits in mice: possible involvement of monoaminergic and gabaergic systems. J Pharmacol Pharmacother 3(1):60–63. https://doi.org/10.4103/0976-500X.92521
Dhingra D, Parle M, Kulkarni SK (2004) Memory enhancing activity of Glycyrrhiza glabra in mice. J Ethnopharmacol 91(2–3):361–365. https://doi.org/10.1016/j.jep.2004.01.016
Dubey T, Chinnathambi S (2019) Brahmi (Bacopa monnieri): an Ayurvedic herb against the Alzheimer’s disease. Arch Biochem Biophys 676:108153. https://doi.org/10.1016/j.abb.2019.108153
Dwivedi KN, Mehra B (2012) Mode of action of medhya drugs: a review. Anc Sci Life 32:83
German R, Rucker G, Tautges J, Wenzl H, Graf E (1978) Isolation and pharmacodynamic activity of the sesquiterpene valeranone from Nardostachys jatamansi DC. Arzneimittelforschung 28(1):7–13
Go J, Park T, Han G, Park H et al (2018) Piperlongumine decreases cognitive impairment and improves hippocampal function in aged mice. Int J Mol Med 42:1875–1884. https://doi.org/10.3892/ijmm.2018.3782
Godkar P, Gordon RK, Ravindran A, Doctor BP (2003) Celastrus paniculatus seed water soluble extracts protect cultured rat forebrain neuronal cells from hydrogen peroxide-induced oxidative injury. Fitoterapia 74:658–669. https://doi.org/10.1016/S0367-326X(03)00190-4
Godkar P, Gordon RK, Ravindran A, Doctor BP (2006) Celastrus paniculatus seed oil and organic extracts attenuate hydrogen peroxide and glutamate-induced injury in embryonic rat forebrain neuronal cells. Phytomedicine 13(1–2):29–36. https://doi.org/10.1016/j.phymed.2003.11.011
Gonzalez-Reyes S, Santillan-Cigales JJ, Jimenez-Osorio AS et al (2016) Glycyrrhizin ameliorates oxidative stress and inflammation in hippocampus and olfactory bulb in lithium/pilocarpine-induced status epilepticus in rats. Epilepsy Res 126:126–133. https://doi.org/10.1016/j.eplepsyres.2016.07.007
Gray NE, Zweig JA, Caruso M et al (2018) Centella asiatica attenuates hippocampal mitochondrial dysfunction and improves memory and executive function in β-amyloid overexpressing mice. Mol Cell Neurosci 93:1–9. https://doi.org/10.1016/j.mcn.2018.09.002
Gupta GL, Fernandes J (2019) Protective effect of Convolvulus pluricaulis against neuroinflammation associated depressive behavior induced by chronic unpredictable mild stress in rat. Biomed Pharmacother 109:1698–1708. https://doi.org/10.1016/j.biopha.2018.11.046
Hanumanthachar J, Navneet K, Jyotibala C (2007) Evaluation of nootropic effect of Argyreia speciosa in mice. J Health Sci 53:382–388. https://doi.org/10.1248/jhs.53.382
Hazzaa SM, Abdelaziz SAM, Eldaim MAA, Daim MAA (2020) Neuroprotective potential of Allium sativum against monosodium glutamate-induced excitotoxicity: impact on short-term memory, gliosis, and oxidative stress. Nutrients 12:1028. https://doi.org/10.3390/nu12041028
Hosamani R, Muralidhar (2009) Neuroprotective efficacy of Bacopa monnieri against rotenone- induced oxidative stress and neurotoxicity in Drosophila melanogaster. NeuroToxicol 30:977–985. https://doi.org/10.1016/j.neuro.2009.08.012
Hosseini M, Mohammadpour T, Karami R et al (2015) Effects of the hydro-alcoholic extract of Nigella Sativa on scopolamine-induced spatial memory impairment in rats and its possible mechanism. Chin J Integr Med 21:438–444. https://doi.org/10.1007/s11655-014-1742-5
Hu KBS, Chen XMS, Chen WMS et al (2018) Neuroprotective effect of gold nanoparticles composites in Parkinson’s disease model. Nanomedicine 14(4):1123–1136. https://doi.org/10.1016/j.nano.2018.01.020
Hua S, Liu J, Zhang Y, Li J, Zhang X, Dong L, Zhao Y, Fu X (2019) Piperine as a neuroprotective functional component in rats with cerebral ischemic injury. Food Sci Nutr 7(11):3443–3451. https://doi.org/10.1002/fsn3.1185
Jaiswal BS, Tailang M (2018) Protective effect of ethanolic extract from the root of Argyreia speciosa against global cerebral ischemic reperfusion injury in rats. J Drug Deliv Ther 8(6):8–15. https://doi.org/10.22270/jddt.v8i6.1990
Joshi H, Parle M (2006) Antiamnesic effect of Desmodium gangeticum in mice. Yakugaku Zasshi 126(9):795–804. https://doi.org/10.1248/yakushi.126.795
Jyoti A, Sharma D (2006) Neuroprotective role of Bacopa monniera extract against aluminium-induced oxidative stress in the hippocampus of rat brain. NeuroToxicol 27(4):451–457. https://doi.org/10.1016/j.neuro.2005.12.007
Kaur M, Goel RK (2009) Anti-convulsant activity of Boerhaavia diffusa plausible role of calcium channel antagonism. Evid Based Complement Alternat Med:310420. https://doi.org/10.1093/ecam/nep192
Khairul M, Sahak A, Mohamed AM et al (2013) Nigella sativa oil enhances the spatial working memory performance of rats on a radial arm maze. Evid Based Complement and Alternat Med:1–5. https://doi.org/10.1155/2013/180598
Khan SM, Ansari IA, Ahamd A et al (2013) Chemotherapeutic potential of Boerhavia diffusa Linn; a review. J Appl Pharma Sci 3(1):133–139. https://doi.org/10.7324/JAPS.2013.30126
Kim J, Kopalli SR, Koppula S (2016) Cuminum cyminum Linn (Apiaceae) extract attenuates MPTP-induced oxidative stress and behavioral impairments in mouse model of Parkinson’s disease. Trop J Pharm Res 15(4):765–772. https://doi.org/10.4314/tjpr.v15i4.14
Kizhakke AP, Olakkaran S, Antony A, Tilagul SK, Hunasanahally GP (2017) Convolvulus pluricaulis (Shankhapushpi) ameliorates human microtubule-associated protein tau (hMAPτ) induced neurotoxicity in Alzheimer’s disease Drosophila model. J Chem Neuroanatomy 95:115–122. https://doi.org/10.1016/j.jchemneu.2017.10.002
Koppula S, Choi DK (2011) Cuminum cyminum extract attenuates scopolamine-induced memory loss and stress-induced urinary biochemical changes in rats: a noninvasive biochemical approach. Pharm Biol 49(7):702–708. https://doi.org/10.3109/13880209.2010.541923
Kosaraju J, Chinni S, Roy PD, Kannan E, Antony AS, Kumar MN (2014) Neuroprotective effect of Tinospora cordifolia ethanol extract on 6-hydroxy dopamine induced parkinsonism. Indian J Pharmacol 46(2):176–180. https://doi.org/10.4103/0253-7613.129312
Kulkarni SK (2005) Handbook of experimental pharmacology, 3rd edn. Vallabh Prakashan, Delhi, India
Kumar A, Sharma V, Singh VP et al (2015) Herbs to curb cyclic nucleotide phosphodiesterase and their potential role in Alzheimer’s disease. Mech Ageing Dev 149:75–87. https://doi.org/10.1016/j.mad.2015.05.009
Kumar R, Arora R, Agarwal A, Gupta YK (2017) Protective effect of Terminalia chebula against seizures, seizure-induced cognitive impairment and oxidative stress in experimental models of seizures in rats. J Ethnopharmacol 215:124–131. https://doi.org/10.1016/j.jep.2017.12.008
Lalert L, Kruevaisayawan H, Amatyakul P, Ingkaninan K, Khongsombat O (2018) Neuroprotective effect of Asparagus racemosus root extract via the enhancement of brain-derived neurotrophic factor and estrogen receptor in ovariectomized rats. J Ethnopharmacol 225:336–341. https://doi.org/10.1016/j.jep.2018.07.014
Lekha G, Kuma BP, Rao SN, Arockiasamy I, Mohan K (2010) Cognitive enhancement and neuroprotective effect of Celastrus paniculatus Willd seed oil (Jyothismati oil) on male wistar rats. J Pharm Sci Tech 2(2):130–138
Limpeanchob N, Jaipan S, Rattanakaruna S, Phrompittayarat W, Ingkaninan K (2008) Neuroprotective effect of Bacopa monnieri on beta-amyloid-induced cell death in primary cortical culture. J Ethnopharmacol 120(1):112–117. https://doi.org/10.1016/j.jep.2008.07.039
Manyam BV (1999) Dementia in Ayurveda. J Altern Complement Med 5(1):81–88. https://doi.org/10.1089/acm.1999.5.81
Mishra R, Kaur G (2013) Aqueous ethanolic extract of Tinospora cordifolia as a potential candidate for differentiation based therapy of glioblastomas. PLoS One 8(10):e78764. https://doi.org/10.1371/journal.pone.0078764
Mishra R, Manchanda S, Gupta M, Kaur T, Saini V, Sharma A, Kaur G (2016) Tinospora cordifolia ameliorates anxiety-like behavior and improves cognitive functions in acute sleep deprived rats. Sci Rep 6:25,564. https://doi.org/10.1038/srep25564
Morzelle MC, Salgado JM, Telles M, Mourelle D, Bachiega P, Buck HS, Viel TA (2016) Neuroprotective effects of pomegranate peel extract after chronic infusion with amyloid-β peptide in mice. PLoS One 11(11):e0166123. https://doi.org/10.1371/journal.pone.0166123
Oh MH, Houghton PJ, Whang WK, Cho JH (2004) Screening of Korean herbal medicines used to improve cognitive function for anti-cholinesterase activity. Phytomedicine 11(6):544–548. https://doi.org/10.1016/j.phymed.2004.03.00gol1
Ojha R, Sahu AN, Muruganandam AV, Singh GK, Krishnamurthy S (2010) Asparagus recemosus enhances memory and protects against amnesia in rodent models. Brain Cogn 74(1):1–9. https://doi.org/10.1016/j.bandc.2010.05.009
Ostergaard M, Larsen A, Stoltenberg M, Penkowa M (2009) Bioreleased gold ions modulate expression of neuroprotective and hematopoietic factors after brain injury. Brain Res 1307:1–13. https://doi.org/10.1016/j.brainres.2009.10.028
Pandey A (2016) Therapeutic potential of Vachadi ghrita (a medicated ghee) on CNS and other ailments—a review. Atreya Ayurveda Foundation Publication 36–46. info:eu-repo/semantics/article
Parihar MS, Hemnani T (2004) Experimental excitotoxicity provokes oxidative damage in mice brain and attenuation by extract of Asparagus racemosus. J Neural Transm (Vienna) 111:1–12. https://doi.org/10.1007/s00702-003-0069-8
Prakash R, Sandhya E, Ramya N, Dhivya R, Priyadarshini M, Sakthi Priya B (2017) Neuroprotective activity of ethanolic extract of Tinospora cordifolia on LPS induced neuroinflammation. Transl Biomed 8(4):135. https://doi.org/10.21767/2172-0479.100135
Rai KS, Murthy KD, Karantha KS, Rao MS (2001) Clitoria ternatea (Linn) root extract treatment during growth spurt period enhances learning and memory in rats. Ind J Physiol Pharmacol 45(3):305–313
Rawal A, Muddeshwar M, Biswas S (2004) Effect of Rubia cordifolia, Fagonia cretica Linn and Tinospora cordifolia on the free radical generation and lipid peroxidation during oxygen-glucose deprivation in rat hippocampal slices. Biochem Biophys Res Commun 324(2):588–596. https://doi.org/10.1016/j.bbrc.2004.09.094
Ray S, Ray A (2015) Medhya Rasayanas in brain function and disease. Med Chem 5(12):505–511. https://doi.org/10.4172/2161-0444.1000309
Revanna G, Pujari S, Subramanian V, Rao SR (2019) Effects of Celastrus paniculatus Willd and Sida cordifolia Linn in kainic acid-induced hippocampus damage in rats. Ind J Pharma Edu Res 53(3):537–544. https://doi.org/10.5530/ijper.53.3.86
Rojanathammanee L, Puig KL, Combs CK (2013) Pomegranate polyphenols and extract inhibit nuclear factor of activated T-cell activity and microglial activation in vitro and in a transgenic mouse model of Alzheimer disease. J Nutr 143(5):597–605. https://doi.org/10.3945/jn.112.169516
Roy C, Mazumdar D (2016) A nootropic effect of Benincasa hispida on ACH and CHAT activity in colchicine induced experimental rat model of Alzheimer’s disease: possible involvement. World J Pharm Res 3(9):1282–1296
Salim S, Ahmad M, Zafar KS, Ahmad AS, Islam F (2003) Protective effect of Nardostachys jatamansi in rat cerebral ischemia. Pharmacol Biochem Behav 74(2):481–486. https://doi.org/10.1016/S0091-3057(02)01030-4
Sastry K, Chaturvedi G (1983) Agnivesha, Caraka Samhita, elaborated Vidyothini hindi commentary, vol 1, 11th edn. Chowkamba Bharathi Academy, Varanasi
Sharma A, Kaur G (2018) Tinospora cordifolia as a potential neuroregenerative candidate against glutamate induced excitotoxicity: an in vitro perspective. BMC Complement Altern Med 18:268. https://doi.org/10.1186/s12906-018-2330-6
Shete RV, Bodhankar SL (2010) Hedychium spicatum: evaluation of its nootropic effect in mice. Res J Pharmacog Phytochem 2(5):403–406
Shinomol GK, Mythri RB, Bharath MMS, Murlidhara (2012) Bacopa monnieri extract offsets rotenone-induced cytotoxicity in dopaminergic cells and oxidative impairments in mice brain. Cell Mol Neurobiol 32(3):455–465. https://doi.org/10.1007/s10571-011-9776-0
Shukla SD, Jain S, Sharma K, Bhatnagar M (2000) Stress induced neuron degeneration and protective effects of Semecarpus anacardium Linn and Withania somnifera Dunn in hippocampus of albino rats: an ultrastructural study. Ind J Exp Biol 38(10):1007–1013
Smith AD, Kelly A (2015) Cognitive processes. The encyclopedia of adulthood and aging:1–4. https://doi.org/10.1002/9781118521373.wbeaa213
Srivastav N, Saxena V (2019) Role of medhyarasayanas (nootropic drugs) in developmental disabilities of children. Int J Health Sci Res 9(6):315–322
Talpate KA, Bhosale UA, Zambare MR, Somani RS (2014) Neuroprotective and nootropic activity of Clitorea ternatea Linn (Fabaceae) leaves on diabetes induced cognitive decline in experimental animals. J Pharm Bioallied Sci 6(1):48–55. https://doi.org/10.4103/0975-7406.124317
Teerapattarakan N, Benya-aphikul H, Tansawat R, Wanakhachornkrai O, Tantisira MH, Rodsiri R (2018) Neuroprotective effect of a standardized extract of Centella asiatica ECa233 in rotenone-induced parkinsonism rats. Phytomedicine 44:65–67. https://doi.org/10.1016/j.phymed.2018.04.028
Tiwari PV (2002) Vriddhajivaka. Suthrasthana, chapter 18. In: Kashyap Samhita. 1st edn. ChaukhambaVisvabharati
Viswanathan G, Mohan V, Radhakrishnan N, Sasikumar A, Prasanna A, Nair R, Baby S (2019) Protection of mouse brain from paracetamol-induced stress by Centella asiatica methanol extract. J Ethnopharmacol 236:474–483. https://doi.org/10.1016/j.jep.2019.03.017
Wang W, Chen X, Zhang J, Zhao Y, Li S, Tan L, Gao J, Fang X, Luo A (2015) Glycyrrhizin attenuates isoflurane-induced cognitive deficits in neonatal rats via its anti-inflammatory activity. Neuroscience 316:328–336. https://doi.org/10.1016/j.neuroscience.2015.11.001
Wichai T, Pannangrong W, Welbat J, Chaichun A, Sripanidkulchai K, Sripanidkulchai B (2019) Effects of aged garlic extract on spatial memory and oxidative damage in the brain of amyloid-ß induced rats. Songklanakarin J Sci Technol 41:311–318
Yamaura K, Nakayama N, Shimada M et al (2012) Antidepressant-like effects of young green barley leaf (Hordeum vulgare L.) in the mouse forced swimming test. Pharm Res 4(1):22–26. https://doi.org/10.4103/0974-8490.91030
Yu XQ, Xue CC, Zhou ZW, Li CG, Du YM, Liang DJ, Zhou SF (2008) In vitro and in vivo neuroprotective effect and mechanisms of glabridin, a major active isoflavan from Glycyrrhiza glabra (licorice). Life Sci 82(1–2):68–78. https://doi.org/10.1016/j.lfs.2007.10.019
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2021 The Author(s), under exclusive license to Springer Nature Singapore Pte Ltd.
About this chapter
Cite this chapter
Ranade, A., Surana, M., Dhokne, S.V., Gaidhani, S., Pawar, S.D. (2021). Ayurvedic Ideology on Rasapanchak-Based Cognitive Drug Intervention. In: Agrawal, D.C., Dhanasekaran, M. (eds) Medicinal Herbs and Fungi. Springer, Singapore. https://doi.org/10.1007/978-981-33-4141-8_18
Download citation
DOI: https://doi.org/10.1007/978-981-33-4141-8_18
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-33-4140-1
Online ISBN: 978-981-33-4141-8
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)