Association of Cell Viability in Huntington Chorea Rat Models and the Neuroprotective Role of Withania Somnifera in Public Health
Abstract:
Huntington’s disorder (HD) is a genetic,
fatal neurodegenerative disorder
that causes abnormal, involuntary jerky movements, postures and defects in
cognition, mood and behaviour. Huntington’s disease involves with degeneration
of neurons in basal nuclei and so has no cure like other neurodegenerative
disorders and the affected person struggles in life for 15-20 years. The basal nuclei are involved in the
inhibition of unwanted motor activities and so responsible for fine motor
movements. Loss of these neurons will inflict on the quality of life of the
person. Neurodegenerative disorders are almost a compulsory evil when a person
is ageing. As nerve cell division and regeneration are impossible, we planned
to analyze the possibility of protecting the neurons already in action by pretreating
them with Withania somnifera, a traditional herbal plant, well known for its
neuroprotective role. We selected 4 groups of experimental rat models, treated
prior with the crude extract of Withania somnifera and the active principle
withanolide A. On analysis, large lesion and dead tissue mass were found in the
brain samples without pretreatment. Wherein brain samples with pretreatment,
the lesion was minimalized and so was the number of dead cells. By analyzing
the actual cell death, we analyzed the protective role of the plant extract and
the active principle we employed. As neurodegeneration is a sure process in age
and regeneration is a question unanswered, prevention or delaying nerve cell
death is a need in the present community health care that was achieved by this
study.
References:
[1]. Young, C. B., Reddy, V., Sonne, J., 2023, Neuroanatomy, Basal ganglia. StatPearls [Internet], Treasure
Island (FL). https://www.ncbi.nlm.nih.gov/books/NBK537141/
[2].
Ogata, S., Miyamoto, Y., Shigematsu, N.,
2022, The tail of the mouse striatum contains a novel large type of GABAergic
Neuron Incorporated in a unique disinhibitory pathway that relays auditory
signals to subcortical nuclei. Journal of
Neuroscience, 42(43),
8078–8094. DOI: 10.1523/JNEUROSCI.2236-21.2022.
[3]. Joshua, W., Callahan, David, L., Wokosin, Mark, D., 2022, Dysregulation of the basal
ganglia indirect pathway in early symptomatic q175 Huntington's
disease mice. Bevan
Journal of Neuroscience, 42(10), 2080-2102. https://doi.org/10.1523/JNEUROSCI.0782-21.2022
[4].
Jain, S., Shukla, S. D., Sharma, K.,
2001, Neuroprotective effects of Withania somnifera Dunn. in hippocampal
sub-regions of the female albino rat. Phytother. Res, 15(6), 544-8. doi: 10.1002/ptr.802.
[5]. Ajitkumar, A., De Jesus, O., 2024, Huntington
Disease. In: StatPearls [Internet]. Treasure Island (FL): StatPearls
Publishing. https://www.ncbi.nlm.nih.gov/books/NBK559166/
[6].
https://www.rarediseaseadvisor.com/disease-info-pages/huntington-disease-epidemiology/#:~:text=They%20estimated%20that%20the%20global,around%202.7%20per%20100%2C000%20persons
[7].
Hussain, Z., Mukherjee,
A., Ganguly, G., Joardar, A., Roy, S., Guin, D. S., Sinharoy, U., Biswas, A.,
Das, S. K., 2020, Clinical profile of genetically proven Huntington's disease
patients from eastern India. Ann Indian Acad Neurol, 23(2), 195-200.
doi: 10.4103/aian.AIAN_505_19. Epub 2020 Feb 25. PMID: 32189861; PMCID:
PMC7061496.
[8].
https://www.deccanherald.com/science/in-focus-huntingtons-disease-762914.html#google_vignette
[9].
Jain, S., Shukla, S. D., Sharma, K.,
2001, Neuroprotective effects of Withania somnifera Dunn. In hippocampal
sub-regions of the female albino rat. Phytother. Res, 15(6), 544-8. doi: 10.1002/ptr.802.
[10].
Gaurav, H., Yadav, D.,
Maurya, A., Yadav, H., Yadav, R., Shukla, A. C., Sharma, M., Gupta, V. K.,
Palazon, J., 2023, Biodiversity,
Biochemical Profiling, and Pharmaco-Commercial Applications of Withania
somnifera: A Review. Molecules. 28, 1208. https://doi.org/10.3390/molecules28031208
[11].
Dhalla, N. S., Gupta, K. C., Sastry, N.
S., 1961, Comparative studies of Withania somnifera dunal and withania ashwagandha kaul. Ind J Pharm, 23(5), 126—127.
[12].
Sukanya, D. H., Lokesha, A. N., Datta, G., 2010, Phytochemical diversity in ashwagandha (Withania somnifera). Home, pp.1-2
[13].
Parihar, M. S., Hemnani, T., 2003, Phenolic antioxidants attenuate hippocampal neuronal cell damage against
kainic acid induced excitotoxicity. J
Biosci, 28(1), 121-8. DOI:10.1007/BF02970142.
[14]. Anjum, A., Cheah, Y. J., Yazid,
M. D., 2022, Protocol paper: kainic acid excitotoxicity-induced spinal cord injury
paraplegia in Sprague–Dawley rats. Biological
Research, 55(38), 1-11. doi: 10.1186/s40659-022-00407-0.
[15]. Elayaraja, A., Vijayalakshmi, M., Devalarao, G., 2010, In vitro free radical scavenging activity of
various root and rhizome extracts of Acorus calamus Linn. Int J Pharma Bio Sci,
1(4), 301.
[16].
Duigou, C., Bouilleret,
V., Miles, R., 2008, Epileptiform activities in slices of hippocampus from mice
after intra-hippocampal injection of kainic acid. J Physiol, 586,
4891-4904. https://doi.org/10.1113/jphysiol.2008.156281
[17]. Ude A, Afi-Leslie
K, Okeke K. Trypan blue exclusion assay, neutral red,
acridine orange and propidium iodide. Cytotoxicity. Intech
Open. 2022; https://doi.org/10.5772/intechopen.105699
[18].
Diwakar, L., Gowaikar,
R., Chithanathan, K. etal. Endothelin-1-mediated
vasoconstriction leads to memory impairment and synaptic dysfunction. Sci Rep. 2021; 11:4868:1-13. https://doi.org/10.1038/s41598-021-84258-x [My paper].
[19].
Jessop, Z. M., Thomas, D. J., Whitaker, I. S., 2022, 3D Bioprinting for
reconstructive surgery. Elsevier Ltd., pp.1-46. ISBN 978-0-08-101103-4. DOI: 10.3390/pharmaceutics14020464.
[20]. Crowley, L. C., Marfell, B. J., Christensen, M. E., 2016, Measuring cell death by trypan blue uptake and light microscopy. Cold Spring Harbor Laboratory Press, 7. doi: 10.1101/pdb. prot087155. PMID: 27371594.