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Biomedical subjects

C R Franci

Publications and source records attributed to C R Franci.

42 records · Page 3Linked to original sources

Water intake in rats subjected to hypothalamic immunoneutralization of angiotensin II, atrial natriuretic peptide, vasopressin, or oxytocin.

To investigate the influence of various peptides on control of dehydration-induced drinking, water intake elicited by overnight water deprivation was analyzed in groups of male rats after intracerebroventricular (third ventricle, icv) injection of 2 microliters of normal rabbit serum or an equal volume of antiserum directed against angiotensin II (Ab-AII), atrial natriuretic peptide, vasopressin, or oxytocin. There was no difference in water intake after normal rabbit serum and antiserum injections when water was offered immediately after icv injections. Water intake was greatly reduced by Ab-AII when water was offered 1 hr and 3 hr after icv injection. The other antisera were partially effective only when water was offered 3 hr after icv injection. The dipsogenic effect of icv injection of AII in normally hydrated rats was reduced only by icv injection of Ab-AII 3 hr before and not by the other antisera. Ab-AII injected icv had no effect on the drinking that occurred just before and after the onset of darkness and that was associated with eating (prandial drinking). The results indicate that AII is primarily responsible for dehydration-induced drinking, and the other peptides may play a permissive role since their antisera were partially effective, with longer latencies after antiserum injection, which is perhaps the result of gradual diffusion to effective sites within the hypothalamus. In contrast, endogenous AII appears to play little, if any, role in prandial drinking.

Angiotensin II↗

Effects of GABA natriuresis induced centrally by cholinergic stimulation.

Sodium and potassium excretion and urine output have been studied in rats following water loading and intracerebroventricular (i.c.v.) injection of isotonic saline (NaCl-0.15M), gamma-amino butyric acid (GABA), picrotoxin, carbachol, GABA plus picrotoxin, GABA plus carbachol and GABA plus atropine. GABA injection decreased sodium and potassium excretion. Picrotoxin or carbachol injection elicited natriuresis and kaliuresis. GABA injection decreased the effects of the carbachol and atropine injection decreased the effects of the GABA on sodium and potassium excretion. These results suggest an interaction between gabaergic and cholinergic pathways in the control of sodium and potassium excretion.

Animals↗

Participation of cholinergic and adrenergic synapses of the medial septal area (MSA) in the natriuretic and kaliuretic responses to intraventricular hypertonic saline (NaCl).

The microinjection of hypertonic sodium chloride into the third ventricle elicits natriuresis and kaliuresis in rats following water loading. These responses were blocked by atropine or phentolamine microinjection into the MSA. The data suggest the interaction between periventricular areas sensible to changes of sodium concentration in the cerebrospinal fluid (CSF) and MSA. Cholinergic and alpha-adrenergic synapses of MSA are involved in this interaction which regulates renal sodium excretion.

Adrenergic Fibers↗

Identification of pathways involved in the natriuretic, kaliuretic and diuretic responses induced by cholinergic stimulation of the medial septal area (MSA).

Natriuresis, kaliuresis and diuresis have been studied in rats following water loading and cholinergic stimulation in the MSA before and after bilateral electrolitic lesion of the habenula, or medullary stria, or supraoptic nucleus or paraventricular nucleus, or fornix. Carbachol injection in MSA elicited an increase of natriuresis and kaliuresis. These responses were blocked by bilateral electrolytic lesion of the habenula, medullary stria, or supraoptic nucleus but not of the paraventricular nucleus or the fornix. Urinary output plotted as a function of time showed antidiuresis in periods of 20 and 40 minutes after carbachol injection into the MSA. The lesion of the supraoptic nucleus inhibited this antidiuresis and natriuresis. The lesion of the habenula or medullary stria blocked natriuresis but not antidiuresis suggesting an independence between the mechanisms of antidiuretic hormone release and natriuresis regulation. The integrity of the habenula, medullary stria and supraoptic nucleus seems to be important in the mediation of the natriuretic response induced by carbachol injection into the MSA.

Animals↗