4.3 Article

Roles of two preoptic cell groups in tonic and febrile control of rat tail sympathetic fibers

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpregu.91010.2008

Keywords

prostaglandin E-2; gamma-aminobutyric acid; heat conservation

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Funding

  1. National Health and Medical Research Council (NHRMC) of Australia [454601]
  2. Robert J. Jr. and Helen C. Kleberg Foundation
  3. Leila Y. and G. Harold Mathers Trust
  4. NHMRC [232305, 454369]

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Tanaka M, McKinley MJ, McAllen RM. Roles of two preoptic cell groups in tonic and febrile control of rat tail sympathetic fibers. Am J Physiol Regul Integr Comp Physiol 296: R1248-R1257, 2009. First published February 11, 2009; doi:10.1152/ajpregu.91010.2008.-In response to cold and in fever, heat dissipation from the skin is reduced by sympathetic vasoconstriction. The preoptic region has been implicated in regulating basal, thermal, and febrile vasoconstriction of cutaneous vessels such as the rat's tail, but the neurons responsible for these functions have not been well localized. We recorded activity from single sympathetic nerve fibers supplying tail vessels in urethane-anesthetized rats, while microinjections of GABA (300 mM, 15-30 nl) were used to inhibit neurons in different parts of the preoptic region. Tail fiber activity increased promptly after GABA injections in two distinct regions: a rostromedial preoptic region (RMPO) centered around the organum vasculosum of the lamina terminalis, and a second region centered similar to 1 mm caudolaterally (CLPO). Responses to GABA within each region were similar. The febrile mediator, PGE(2) (0.2 or 1 ng in 15 nl) was then microinjected into GABA-sensitive preoptic sites. Injections of PGE(2) into the RMPO induced a rapid increase in tail fiber activity followed by a rise in core temperature; injections into the rostromedial part of CLPO gave delayed tail fiber responses; injections into the central and caudal parts of CLPO were without effect. These results indicate that neurons in two distinct preoptic regions provide tonic inhibitory drive to the tail vasoconstrictor supply, but febrile vasoconstriction is mediated by PGE(2) selectively inhibiting neurons in the rostromedial region.

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