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allied

academies

March 14-16, 2019 | London, UK

12

th

International Conference on

8

th

International Conference on

Vascular Dementia and Dementia

Neurological Disorders and Stroke

Joint Event

&

Journal of Brain and Neurology | Volume 3

Trpv channels in the Brain and Pituitary: Organization and possible role

Santosh Kumar

1

and

Praful Singru

2

1

University of California Davis, USA

2

National Institute of Science Education and Research, India

T

ransient receptor potential vanilloid (Trpv) subfamily of

cation channels have emerged as novel regulators of

neural and neuroendocrine regulation. Trpv ion channels

are polymodal in nature and activated by a range of agents/

stimuli. In recent years estradiol has emerged as a potential

regulator of Trpv channels in the peripheral tissues and

sensory neurons, however, its analogous role in the CNS is

poorly understood. Trpv channels modulate Ca2+ signaling,

neurotransmission and behavior, and expression of these

ion channels and estrogen receptors show a great degree of

overlap in different brain regions. The promoter of Trpv1-6

genes contain estrogen response element and we observed

estrous cycle-related changes in their expression in different

brain compartments. In view of the higher Ca2+-selectivity

and estrogen responsiveness, we have demonstrated the

neuroanatomical organization of Trpv5 and Trpv6-ir elements in

the brain. We observed wide distribution of Trpv5- and Trpv6-

equipped elements in the brain. Trpv5-ir was present in neurons

as well as glial cells, whereas Trpv6-ir was observed in neuronal

cell bodies and fibers. These ion channels expressing elements

were observed in the hypothalamic cocaine-and amphetamine-

regulated transcript (CART), neuropeptide Y (NPY), oxytocin

and vasopressin neurons. Further, CART neurons expressing

Trpv5 and Trpv6-ir neurons in the hypothalamus coexpressing

ERα showed estrous cycle-dependent changes. Given the

discretely organized Trpv1-6-ir elements in different lobes of

the pituitary gland, we speculate that Trpv ion channels as novel

endocrine regulators of pituitary gland. We found the presence

of Trpv1 in growth hormone (GH) cells and treatment with

Trpv1 agonist stimulated GH secretion in rat pituitary primary

cultures. Interestingly, the CART-induced GH release seems

independent of Trpv1. The findings are important since Trpv1 is

thermosensitive, temperature is an important regulator of GH

secretion, and GH release has been shown to increase with an

increase in the core body temperature during exercise.

Speaker Biography

Santosh Kumar has completed his PhD in April 2018 from the National Institute of Science

Education and Research, Bhubaneswar, India. He worked on the neural pathways that link

energy balance and reproduction, and explored the role of Trpv channels in the brain and

pituitary. He has 12 publications of which 4 are first author published in Neuroscience,

Journal of Neuroendocrinology, and Brain Research. At present, he is working on the

mechanisms of neurodevelopmental disorders at the University of California, Davis, USA

as a postdoctoral scholar.

e:

santoshkumarbio@gmail.com