TY - JOUR
T1 - Heat acclimation affects the neuromodulatory role of AngII and nitric oxide during combined heat and hypohydration stress
AU - Schwimmer, H.
AU - Gerstberger, R.
AU - Horowitz, M.
PY - 2004/11/4
Y1 - 2004/11/4
N2 - We studied the effect of heat acclimation on the neuromodulatory role of angiotensin (AngII) and nitric oxide during combined heat (39°C) and hypohydration (water deprivation, -10% body weight) stress. Rats were divided into control (C), short (2d-STHA) or long (30d-LTHA) acclimation (34°C) groups. AngII, 7-nitroindazole (7NI)-nNOS blocker, or both were centrally administered (5 μl, bolus) under light chloroform anesthesia prior to each experimental paradigms: (1) In vivo: measurements of skin-vasodilatation (VTsh) and salivation-cooling (STsh) thresholds, and heat endurance in conscious heat/hypohydrated stressed rats; (2) expression of AT 1 and AT 2 AngII receptors and nNOS were measured in the hypothalamus (Western blot); (3) transcript levels of the coding genes were measured using real-time PCR. A synthesis of the results shows a biphasic acclimatory profile of VTsh, STsh, and transcript levels of all studied genes, with transient up/down-regulatory changes on STHA. AngII affected the physiological integrative outcome primarily during euhydration, although AT membranal changes (except in LTHA) were confined to hypohydration. 7NI had an impact during hypohydration. Evidence is provided that AngII and 7NI modulate thermoregulation primarily via AT 1 and AT 2 receptors, with predominance of AT 2 signaling following LTHA and/or hypohydration, opposing a drop in AT 1-mediated thresholds. The final shaping of AngII signaling depends on cross-talk between nNOS and AngII receptors at both molecular and protein levels. Hypohydration induces transcriptional responses but desensitizes AngII receptors signaling, attenuating their effect on VTsh and STsh, and abolishing the beneficial thermoregulatory effects achieved by heat acclimation. nNOS, AngII receptor-independent pathway is also implicated.
AB - We studied the effect of heat acclimation on the neuromodulatory role of angiotensin (AngII) and nitric oxide during combined heat (39°C) and hypohydration (water deprivation, -10% body weight) stress. Rats were divided into control (C), short (2d-STHA) or long (30d-LTHA) acclimation (34°C) groups. AngII, 7-nitroindazole (7NI)-nNOS blocker, or both were centrally administered (5 μl, bolus) under light chloroform anesthesia prior to each experimental paradigms: (1) In vivo: measurements of skin-vasodilatation (VTsh) and salivation-cooling (STsh) thresholds, and heat endurance in conscious heat/hypohydrated stressed rats; (2) expression of AT 1 and AT 2 AngII receptors and nNOS were measured in the hypothalamus (Western blot); (3) transcript levels of the coding genes were measured using real-time PCR. A synthesis of the results shows a biphasic acclimatory profile of VTsh, STsh, and transcript levels of all studied genes, with transient up/down-regulatory changes on STHA. AngII affected the physiological integrative outcome primarily during euhydration, although AT membranal changes (except in LTHA) were confined to hypohydration. 7NI had an impact during hypohydration. Evidence is provided that AngII and 7NI modulate thermoregulation primarily via AT 1 and AT 2 receptors, with predominance of AT 2 signaling following LTHA and/or hypohydration, opposing a drop in AT 1-mediated thresholds. The final shaping of AngII signaling depends on cross-talk between nNOS and AngII receptors at both molecular and protein levels. Hypohydration induces transcriptional responses but desensitizes AngII receptors signaling, attenuating their effect on VTsh and STsh, and abolishing the beneficial thermoregulatory effects achieved by heat acclimation. nNOS, AngII receptor-independent pathway is also implicated.
KW - AngII receptors
KW - Heat-acclimation
KW - Hypohydration
KW - Neuromodulation
KW - nNOS
KW - Thermoregulation
UR - http://www.scopus.com/inward/record.url?scp=7444259171&partnerID=8YFLogxK
U2 - 10.1016/j.molbrainres.2004.07.011
DO - 10.1016/j.molbrainres.2004.07.011
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C2 - 15519680
AN - SCOPUS:7444259171
SN - 0169-328X
VL - 130
SP - 95
EP - 108
JO - Molecular Brain Research
JF - Molecular Brain Research
IS - 1-2
ER -