Neurogenic Potential of Clitoria ternatea Aqueous Root Extract–A Basis for Enhancing Learning and Memory
Commenced in January 2007
Frequency: Monthly
Edition: International
Paper Count: 32797
Neurogenic Potential of Clitoria ternatea Aqueous Root Extract–A Basis for Enhancing Learning and Memory

Authors: Kiranmai S.Rai

Abstract:

The neurogenic potential of many herbal extracts used in Indian medicine is hitherto unknown. Extracts derived from Clitoria ternatea Linn have been used in Indian Ayurvedic system of medicine as an ingredient of “Medhya rasayana", consumed for improving memory and longevity in humans and also in treatment of various neurological disorders. Our earlier experimental studies with oral intubation of Clitoria ternatea aqueous root extract (CTR) had shown significant enhancement of learning and memory in postnatal and young adult Wistar rats. The present study was designed to elucidate the in vitro effects of 200ng/ml of CTR on proliferation, differentiation and growth of anterior subventricular zone neural stem cells (aSVZ NSC-s) derived from prenatal and postnatal rat pups. Results show significant increase in proliferation and growth of neurospheres and increase in the yield of differentiated neurons of aSVZ neural precursor cells (aSVZNPC-s) at 7 days in vitro when treated with 200ng/ml of CTR as compared to age matched control. Results indicate that CTR has growth promoting neurogenic effect on aSVZ neural stem cells and their survival similar to neurotrophic factors like Survivin, Neuregulin 1, FGF-2, BDNF possibly the basis for enhanced learning and memory.

Keywords: Anterior subventricular zone (aSVZ) neural stemcell, Clitoria ternatea, Learning and memory, Neurogenesis.

Digital Object Identifier (DOI): doi.org/10.5281/zenodo.1074966

Procedia APA BibTeX Chicago EndNote Harvard JSON MLA RIS XML ISO 690 PDF Downloads 2959

References:


[1] K. G. Bath, F.S.Lee, "Neurotrophic factor control of adult SVZ neurogenesis ," in Developmental Neurobiology , Special Issue:trophic Factors:50 years of growth . vol. 70, no.5, pp. 339-349 April 2010.
[2] Y.Ganat,S.Soni,M.Chacon,M.L.Schwartz and F.M.Vaccarino, Neuroscience,vol.112,no. 4, pp. 977-991,July 2002.
[3] A.Alvarez-Byulla and J.M. Garcia -Verdugo, "Neurogenesis in adult subventricular zone," The Journal of Neuroscience,vol 22,no. 3,pp. 629- 634,Feb, 2002.
[4] S.Temple, "The development of neural stem cells," Nature, vol. 414, pp. 112-117 2001.
[5] S.W.Levison and J.E.Goldman, "Both oligodendrocytes and astrocytes develop from progenitors in the subventricular zone of postnatal rat forebrain," Neuron, vol.15, pp. 7238-7249,1995.
[6] M.Zerlin,S.W.Levison and J.E.Goldman, "Early patterns of migration,morphogenesis and intermediate filament expression of subventricular zone cells in the postnatal rat forebrain," Journal of Neuroscience., vol.10, no.2, pp. 201-212,Feb,1993.
[7] D.A.Lim,G.J.Fishell and A.Alvarez-Byulla, "A postnatal mouse subventricular zone neuronal precursors can migrate and differentiate within multiple levels of the developing neuraxis," Proc Natl Acad Sci USA, vol.94, pp. 14832-14836,1997.
[8] R.Zhang,Z.Zhang,L.Wang,Y.Wang,A.Gousev,L.Zhang,et.al,"Activated neural stem cells contribute to stroke-induced neurogenesis and neuroblast migration towards the infarct boundary in adult rats," Journal of Cerebral Blood Flow & Metabolism, vol.24, pp. 441-448,2004.
[9] V.Coremans,T.Ahmed,D.Balschun,R.D-Hooge,A.DeVriese,J.Cremer,et. al, "Impaired neurogenesis, learning and memory and low seizure threshold associated with loss of neural precursor cell survivin," BMC Neurosci., vol. 11, pp. 2,Jan. 2010.
[10] K.Ohira, T.Furuta, H.Hioki, K.C.Nakamura, E.Kuramoto, Y.Tanaka, et.al.,"Ischemia-induced neurogenesis of neocortical layer 1 progenitor cells," Nature Neurosci., vol. 13, no.2, pp.173-179,Feb.2010.
[11] Y.Liu, B.D.Ford, M.A.Mann, G.D.Fischbach, "Neuregulin-1 increases the proliferation of neuronal progenitors from embryonic neural stem cells," Developmental Biology, vol. 283, pp. 437-445, 2005.
[12] K.S.Rai, B.Hattiangady, A.K.Shetty , "Enhanced production and dendritic growth of new dentate granule cells in the middle- aged hippocampus following intracerebroventricular FGF-2 infusions," Eur J Neurosci, vol. 26,no.7, pp. 1765-1779, Oct 2007.
[13] H.Scharfman,J.Goodman,A.Macleod,S.Phani,C.Antonelli,S.Croll, "Increased neurogenesis and the ectopic granule cells after intrahippocampal BDNF infusions in adult rats," Exp.Neurol., vol. 192, no. 2, pp. 348-356, Apr. 2005.
[14] K.Jin,Y.Sun,L.Xie,S.Batteur,X.O.Mao,C.Smelick,A.Logvinova,D.A.Gre enberg,"Neurogenesis and aging:FGF-2 and HB-EGF restore neurogenesis in hippocampus and subventricular zone of aged mice," Aging Cell, vol. 2,no.3,pp.175-183,June 2003.
[15] K.S.Rai, K.D.Murthy, K.S.Karanth, M.S.Rao, "Clitoria ternatea (Linn) root extract during growth spurt period enhances learning and memory in rats," Indian J. Physiol Pharmacol, vol.45,pp. 305-313,2001.
[16] K.S.Rai, K.D.Murthy, M.S.Rao, K.S.Karanth, "Clitoria ternatea (Linn) root extract treatment in rats during growth spurt period affects dendritic morphology of hippocampal CA3 neurons," In Third Congress. Federation of Indian Physiological Societies (FIPS), Calcutta (Abstract no. 4.5),pp. 45,2000.
[17] K.S.Rai, K.D.Murthy, K.S.Karanth, K.Nalini, M.S.Rao,K.K.Srinivasan, "Clitoria ternatea root extract enhances acetylcholine content in rat hippocampus," Fitoterapia, vol.73,pp. 685-689,2002.
[18] K.S.Rai, K.D.Murthy, M.S.Rao, K.S.Karanth, "Altered dendritic arborization of amygdala neurons in young adult rats orally intubated with Clitoria ternatea aqueous root extract," Phytotherapy Research, vol.19,pp. 592-598,2005.
[19] A.K.Shetty, "Progenitor cells from the CA3 region of the embryonic day 19 rat hippocampus generate region-specific neuronal phenotypes in vitro," Hippocampus, vol.14, no.5, pp. 595-614, 2004.
[20] V.Darsalia, U.Heldmann, O.Lindvall, Z.Kokaia,"Stroke-induced neurogenesis in aged brain," Stroke, vol.36, pp.1790-1795, 2005.
[21] J.Macas, C.Nern, K.H.Plate and S.Momma,"Increased generation of neural progenitors after ischemic injury in the aged adult human forebrain," The Journal of Neuroscience, vol.26,no.50, pp.13114-13119, Dec 2006.
[22] G.Xu, J.Ong, Y-Q.Liu, F.S.Silverstein, J.D.E.Barks,"Subventricular zone proliferation after ╬▒-amino-3-hydroxy-5-methyl-4- isoxazolepropionic acid receptor-mediated neonatal brain injury," Developmental Neuroscience, vol.27,no.2-4, pp.228-234, 2005.
[23] B.Nait-Oumesmar, N.Picard-Riera, C.Kerninon, A.Baron VanEvercooren, "The role of SVZ- derived neural precursors in demyelinating diseases: From animal models to multiple sclerosis," Journal of the Neurological Sciences, vol.265, no.1-2, pp.26-31,Feb. 2008.
[24] H.Okana, M.Sakaguchi, K.Ohki, N.Suzuki,and K.Sawamoto, "Regeneration of the central nervous system using endogenous repair mechanisms," Journal of Neurochemistry, vol.102, pp.1459-1465,2007.
[25] H.M.Sisti, A.L.Glass and T.J.Shors, "Neurogenesis and the spacing effect: Learning over time enhances memory and the survival of new neurons," Learning and Memory, vol.14, pp.368-375, 2007.
[26] G.Kempermann, "The neurogenic reserve hypothesis:What is adult hippocampal neurogenesis good for?," Trends Neurosci., vol.31, no. 4, pp.163-169, Mar.2008.
[27] J.Lee, W.Duan and M.P.Mattson, "Evidence that brain-derived neurotrophic factor is required for basal neurogenesis and mediates, in part,the enhancement of neurogenesis by dietary restriction in the hippocampus of adult mice," Journal of Neurochemistry., vol.82, pp.1367-1375, 2002.
[28] A.K.Olson, B.D.Eadie, C.Ernst and B.R.Christie, "Environmental enrichment and voluntary exercise massively increase neurogenesis in the adult hippocampus via dissociable pathways," Hippocampus, Special issue on Neurogenesis, vol.16, no.3, pp.250-260, Jan.2006.