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Am J Physiol Regul Integr Comp Physiol 275: R234-R244, 1998;
0363-6119/98 $5.00
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Vol. 275, Issue 1, R234-R244, July 1998

Central angiotensin AT1 and muscarinic receptors in ITF expression on intracerebroventricular NaCl

E. Moellenhoff, C. J. Lebrun, A. Blume, J. Culman, T. Herdegen, and T. Unger

Institute of Pharmacology, University of Kiel, 24105 Kiel; and German Institute for High Blood Pressure Research, 69120 Heidelberg, Germany

In the present study, we investigated the expression pattern of the inducible transcription factors (ITF) c-Fos, c-Jun, JunB, JunD, and Krox-24 following intracerebroventricular injections of hyperosmolar saline (0.2, 0.3, and 0.6 M NaCl) and its mediation via angiotensin and/or muscarinic receptors. c-Fos, c-Jun, and Krox-24 were differentially expressed in organum vasculosum laminae terminalis, median preoptic area, subfornical organ (SFO), and paraventricular and supraoptic nuclei. Expression of c-Fos and c-Jun was inhibited by pretreatment with the angiotensin AT1 receptor antagonist losartan (10 and 20 nmol icv) following 0.20 and 0.30 M saline. Pretreatment with atropine (15 nmol icv) inhibited the 0.30 and 0.60 M NaCl-induced expression of c-Fos, c-Jun, and Krox-24 in all areas except the SFO. Coexpression of the ITF with vasopressin and oxytocin, the major effector peptides in osmoregulation, was demonstrated, implying the corresponding genes as putative target genes of the ITF. The results show a highly differentiated ITF expression pattern in the brain mediated by angiotensinergic and muscarinergic pathways, suggesting a finely tuned regulation of target genes.

central osmoregulation; c-Fos; c-Jun; Krox-24; losartan; atropine





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