Cholinergic receptor subtypes functional regulation in spinal cord injured monoplegic rats

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Cholinergic receptor subtypes functional regulation in spinal cord injured monoplegic rats

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dc.contributor.author Chinthu, Romeo
dc.contributor.author Dr. Paulose, C S
dc.date.accessioned 2013-10-28T04:31:23Z
dc.date.available 2013-10-28T04:31:23Z
dc.date.issued 2012-08-17
dc.identifier.uri http://dyuthi.cusat.ac.in/purl/3046
dc.description Department of Biotechnology, Cochin University of Science and Technology en_US
dc.description.abstract The present study deals with the Cholinergic Receptor subtypes functional regulation in spinal cord injured monoplegic rats: Effect of 5-HT GABA and bone marrow cells.Spinal cord injury causes permanent and irrevocable motor deficits and neurodegeneration. Disruption of the spinal cord leads to diminished transmission of descending control from the brain to motor neurons and ascending sensory information. Behavioural studies showed deficits in motor control and coordination in SCI rats. Cholinergic system plays an important role in SCI, the evaluation of which provides valuable insight on the underlying mechanisms of motor deficit that occur during SCI. The cholinergic transmission was studied by assessing the muscarinic and nicotinic receptors; cholinergic enzymes- ChAT and AChE; second messenger enzyme PLC; transcription factor CREB and second messengers - IP3, cAMP and cGMP. We observed a decrease in the cholinergic transmission in the brain and spinal cord of SCI rats. The disrupted cholinergic system is the indicative of motor deficit and neuronal degeneration in the spinal cord and brain regions. SCI mediated oxidative stress and apoptosis leads to neuronal degeneration in SCI rats. The decreased expression of anti oxidant enzymes – SOD, GPx and neuronal cell survival factors - BDNF, GDNF, IGF-1, Akt and cyclin D2 along with increased expression of apoptotic factors – Bax, caspase-8, TNFa and NF-kB augmented the neuronal degeneration in SCI condition. BMC administration in combination with 5-HT and GABA in SCI rats showed a reversal in the impaired cholinergic neurotransmission and reduced the oxidative stress and apoptosis. It also enhanced the expression of cell survival factors in the spinal cord region. In SCI rats treated with 5-HT and GABA, the transplanted BMC expressed NeuN confirming that 5-HT and GABA induced the differentiation and proliferation of BMC to neurons in the spinal cord. Neurotrophic factors and anti-apoptotic elements in SCI rats treated with 5-HT and GABA along with BMC rendered neuroprotective effects accompanied by improvement in behavioural deficits. This resulted in a significant reversal of altered cholinergic neurotransmission in SCI. The restorative and neuro protective effects of BMC in combination with 5-HT and GABA are of immense therapeutic significance in the clinical management of SCI. en_US
dc.description.sponsorship Cochin University of Science and Technology en_US
dc.language.iso en en_US
dc.publisher Cochin University of Science and Technology en_US
dc.subject Spinal cord injury(SCI) en_US
dc.subject Current treatments and its side effects in spinal cord injury en_US
dc.subject Acetylcholine en_US
dc.subject Neuronal survival factors in spinal cord injury en_US
dc.subject Cell therapy in SCI en_US
dc.subject Apoptosis &Spinal cord Injury en_US
dc.title Cholinergic receptor subtypes functional regulation in spinal cord injured monoplegic rats en_US
dc.title.alternative Effect of 5-HT, GABA and Bone Marrow Cells en_US
dc.type Thesis en_US


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