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Alterations in the water intake caused by central inhibition of angiotensin-converting enzyme in the rat

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Elsevier B.V.

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In the present study we investigated the effects of central (i.c.v.) and subcutaneous (s.c.) injections of a 2 μg dose of lisinopryl, an inhibitor of angiotensin I(ANGI)-converting enzyme (CE), on water intake. I.c.v. but not s.c. injection of lisinopryl abolished drinking in response to s.c. isoprenaline (100 μg/kg) and significantly reduced drinking in response to 24 h water deprivation or s.c. polyethylene glycol (30% w/v, 10 ml/kg). Lisinopryl had no effect on water intake induced by cellular dehydration (s.c. injection of hypertonic saline (2 M NaCl)). These results are consistent with the hypothesis that lisinopryl acts as a CE blocking agent in the brain. The thirst challenge induced by hypotension using isoprenaline acts primarily by generating ANGII systemically and centrally. The other thirst challenges such as cellular dehydration are independent of the ANGII in the brain. This conclusion was made possible by utilizing a new CE blocking agent at a smaller dose than normally used for other ANG I-CE inhibitors. © 1992.

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Angiotensin, Lateral ventricle, Lisinopryl, Water intake, Lisinopril, Animal experiment, Fluid intake, Intracerebroventricular drug administration, Male, Nonhuman, Priority journal, Rat, Subcutaneous drug administration, Angiotensin-Converting Enzyme Inhibitors, Animal, Cerebral Ventricles, Drinking Behavior, Enalapril, Injections, Intraventricular, Injections, Subcutaneous, Isoproterenol, Lisinopril, Male, Rats, Reference Values, Saline Solution, Hypertonic, Support, Non-U.S. Gov't, Time Factors

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Inglês

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Neuroscience Letters. Clare: Elsevier Sci Ireland Ltd, v. 134, n. 2, p. 212-214, 1992.

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