To further explore the interaction between opiates and catecholamines in the control of water balance, we studied the effects of the alpha 1-adrenoceptor antagonist dapiprazole on the modifications in drinking and diuresis produced by U-50,488H (a selective kappa-opiate agonist), morphine, naloxone, and amphetamine in rats. Because animals were maintained in a free-feeding paradigm and water intake is also controlled by feeding (prandial drinking), food intake was also measured. At doses administered (3-6 mg/kg, IP), dapiprazole had no effect on basal food and water intake or on diuresis. Nor did it modify changes in feeding and drinking produced by U-50,488H, morphine, naloxone, and amphetamine. It did, however, antagonize the diuretic effect of both U-50,488H and amphetamine. In addition, suppression of diuresis was obtained by combining doses of dapiprazole and morphine or naloxone that were devoid of antidiuretic effects when administered independently. A further experiment showed that diuresis produced by water load was also prevented by dapiprazole. alpha 1-Adrenoceptors thus appear to play a role in the regulation of water balance in a condition of free access to water, inhibiting diuresis without affecting drinking.

The alpha 1-blocker dapiprazole inhibits diuresis but not drinking and feeding induced by U-50,488H / Nencini, Paolo; P., Valeri; G., Pimpinella. - In: BRAIN RESEARCH BULLETIN. - ISSN 0361-9230. - 29:(1992), pp. 401-405. [10.1016/0361-9230(92)90075-9]

The alpha 1-blocker dapiprazole inhibits diuresis but not drinking and feeding induced by U-50,488H.

NENCINI, Paolo;
1992

Abstract

To further explore the interaction between opiates and catecholamines in the control of water balance, we studied the effects of the alpha 1-adrenoceptor antagonist dapiprazole on the modifications in drinking and diuresis produced by U-50,488H (a selective kappa-opiate agonist), morphine, naloxone, and amphetamine in rats. Because animals were maintained in a free-feeding paradigm and water intake is also controlled by feeding (prandial drinking), food intake was also measured. At doses administered (3-6 mg/kg, IP), dapiprazole had no effect on basal food and water intake or on diuresis. Nor did it modify changes in feeding and drinking produced by U-50,488H, morphine, naloxone, and amphetamine. It did, however, antagonize the diuretic effect of both U-50,488H and amphetamine. In addition, suppression of diuresis was obtained by combining doses of dapiprazole and morphine or naloxone that were devoid of antidiuretic effects when administered independently. A further experiment showed that diuresis produced by water load was also prevented by dapiprazole. alpha 1-Adrenoceptors thus appear to play a role in the regulation of water balance in a condition of free access to water, inhibiting diuresis without affecting drinking.
1992
3; 4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide; (trans)-Isomer, Adrenergic alpha-Antagonists; pharmacology, Amphetamine; pharmacology, Analgesics; antagonists /&/ inhibitors/pharmacology, Animals, Diuresis; drug effects, Drinking Behavior; drug effects, Feeding Behavior; drug effects, Male, Piperazines, Pyrrolidines; antagonists /&/ inhibitors/pharmacology, Rats, Rats; Sprague-Dawley, Triazoles; pharmacology, Urination, Water-Electrolyte Balance; drug effects
01 Pubblicazione su rivista::01a Articolo in rivista
The alpha 1-blocker dapiprazole inhibits diuresis but not drinking and feeding induced by U-50,488H / Nencini, Paolo; P., Valeri; G., Pimpinella. - In: BRAIN RESEARCH BULLETIN. - ISSN 0361-9230. - 29:(1992), pp. 401-405. [10.1016/0361-9230(92)90075-9]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/452705
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