Detailed Information on Publication Record
2016
TRPV currents and their role in the nociception and neuroplasticity
SATHEESH, Noothan Jyothi, Yoshio UEHARA, Julia FEDOTOVA, Miroslav POHANKA, Dietrich BUSSELBERG et. al.Basic information
Original name
TRPV currents and their role in the nociception and neuroplasticity
Authors
SATHEESH, Noothan Jyothi (634 Qatar), Yoshio UEHARA (392 Japan), Julia FEDOTOVA (643 Russian Federation), Miroslav POHANKA (203 Czech Republic), Dietrich BUSSELBERG (634 Qatar) and Peter KRUŽLIAK (703 Slovakia, guarantor, belonging to the institution)
Edition
NEUROPEPTIDES, EDINBURGH, CHURCHILL LIVINGSTONE, 2016, 0143-4179
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30202 Endocrinology and metabolism
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 2.486
RIV identification code
RIV/00216224:14110/16:00100475
Organization unit
Faculty of Medicine
UT WoS
000378193100001
Keywords in English
TRPV receptors; Currents; Nociception; Neuroplasticity; Therapy
Tags
Tags
International impact, Reviewed
Změněno: 11/5/2018 15:17, Soňa Böhmová
Abstract
V originále
Transient receptor potential channels sensitive to vanilloids (TRPVs) are group of ion channels which are sensitive to various tissue damaging signals and their activation is generally perceived as pain. Therefore, they are generally named as nociceptors. Understanding their activation and function as well as their interaction with intracellular pathways is crucial for the development of pharmacological interference in order to"reduce pain perception. The current review summarizes basic facts in regard to TRPV and discusses their relevance in the sensing of (pain-) signals and their intracellular processing, focussing on their modulation of the intracellular calcium ([Ca2+](i)) signal. Furthermore we discuss the basic mechanisms how the modification of [Ca2+](i) through TRPV might induce long-term-potentiation (LTP) or long-term- depression (LTD) and from "memories" of pain. Understanding of these mechanisms is needed to localize the best point of interference for pharmacological treatment. Therefore, high attention is given to highlight physiological and pathological processes and their interaction with significant modulators and their roles in neuroplasticity and pain modulation. (C) 2016 Elsevier Ltd. All rights reserved.