HYDROGEN SULFIDE AS A CRYOGENIC MEDIATOR OF HYPDXIA-INDUCED ANAPYREXIA
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
---|---|
Data(s) |
05/11/2013
05/11/2013
2012
|
Resumo |
Hypoxia causes a regulated decrease in body temperature (Tb), a response that has been aptly called anapyrexia, but the mechanisms involved are not completely understood. The roles played by nitric oxide (NO) and other neurotransmitters have been documented during hypoxia-induced anapyrexia, but no information exists with respect to hydrogen sulfide (H(2)S), a gaseous molecule endogenously produced by cystathionine beta-synthase (CBS). We tested the hypothesis that HA production is enhanced during hypoxia and that the gas acts in the anteroventral preoptic region (AVPO; the most important thermosensitive and thermointegrative region of the CNS) modulating hypoxia-induced anapyrexia. Thus, we assessed CBS and nitric oxide synthase (NOS) activities [by means of H2S and nitrite/nitrate (NO(x)) production, respectively] as well as cyclic adenosine 3',5'-monophosphate (cAMP) and cyclic guanosine 3',5'-monophosphate (cGMP) levels in the anteroventral third ventricle region (AV3V; where the AVPO is located) during normoxia and hypoxia. Furthermore, we evaluated the effects of pharmacological modifiers of the H2S pathway given i.c.v. or intra-AVPO. I.c.v. or intra-AVPO microinjection of CBS inhibitor caused no change in Tb under normoxia but significantly attenuated hypoxia-induced anapyrexia. During hypoxia there were concurrent increases in H2S production, which could be prevented by CBS inhibitor, indicating the endogenous source of the gas. cAMP concentration, but not cGMP and NOR, correlated with CBS activity. CBS inhibition increased NOS activity, whereas H2S donor decreased NO. production. In conclusion, hypoxia activates H2S endogenous production through the CBS-H(2)S pathway in the AVPO, having a cryogenic effect. Moreover, the present data are consistent with the notion that the two gaseous molecules, H(2)S and NO, play a key role in mediating the drop in Tb caused by hypoxia and that a fine-balanced interplay between NOS-NO and CBS-H(2)S pathways takes place in the AVPO of rats exposed to hypoxia. (C) 2011 IBRO. Published by Elsevier Ltd. All rights reserved. Fundagao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) Fundagao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) Conselho Nacional de Desenvolvimento Cientifico e TecnolOgico (CNPq) Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) Coordenagao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES), Brazil Coordenagao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES), Brazil [2010/50882-1] |
Identificador |
NEUROSCIENCE, OXFORD, v. 201, n. 3, supl. 4, Part 1-2, pp. 146-156, 40179, 2012 0306-4522 http://www.producao.usp.br/handle/BDPI/41326 10.1016/j.neuroscience.2011.11.030 |
Idioma(s) |
eng |
Publicador |
PERGAMON-ELSEVIER SCIENCE LTD OXFORD |
Relação |
NEUROSCIENCE |
Direitos |
closedAccess Copyright PERGAMON-ELSEVIER SCIENCE LTD |
Palavras-Chave | #AVPO #HYPOTHERMIA #H(2)S #AMINOOXYACETATE #CBS #HYPOTHALAMUS #ANTEROVENTRAL PREOPTIC REGION #HYPOXIA-INDUCED ANAPYREXIA #CENTRAL-NERVOUS-SYSTEM #NITRIC-OXIDE SYNTHASE #3RD VENTRICLE AV3V #FACTOR-KAPPA-B #CARBON-MONOXIDE #CYCLIC-AMP #HEME OXYGENASE #INDUCIBLE CYCLOOXYGENASE #NEUROSCIENCES |
Tipo |
article original article publishedVersion |