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1.
Indian J Physiol Pharmacol ; 1996 Jan; 40(1): 87-90
Article in English | IMSEAR | ID: sea-107734

ABSTRACT

In water loaded (5 ml/100 g) unanesthetized rats. nitrendipine (NT), nimodipine (NM) and nisoldipine (NS) (5 mg/ kg, i.p.) caused significant (P < 0.01) increase in water and Na+ excretion. However, there was no significant increase in K+ excretion after NT, NM and NS administration. NS was more potent in increasing excretion of water load as compared to NT and NM. The glomerular filtration rate as assessed by creatinine clearance, was significantly (P < 0.01) increased in NT, NM and NS (5 mg/kg, i.p.) treated groups as compared to control. The mean creatinine clearance values after NT, NM and NS were 26.95 +/- 0.35, 22.11 +/- 0.72 and 28.13 +/- 0.95 respectively as compared to 22.19 +/- 0.51, 18.77 +/- 0.42 and 22.97 +/- 0.60 in corresponding control groups. The results of the study suggest that in addition to other effects, NT, NM and NS have a selective inhibitory effect on Na+ handling mechanisms in the nephron.


Subject(s)
Animals , Calcium Channel Blockers/pharmacology , Creatinine/blood , Diuresis/drug effects , Electrolytes/urine , Female , Glomerular Filtration Rate , Male , Nimodipine/pharmacology , Nisoldipine/pharmacology , Nitrendipine/pharmacology , Rats
2.
Indian J Exp Biol ; 1995 Jun; 33(6): 420-3
Article in English | IMSEAR | ID: sea-61312

ABSTRACT

Cardiac necrosis was produced in rats by administering isoproterenol sulphate (85 mg/kg, sc for 4 days). The myocardial damage was proved by observing the elevated levels of serum aspartate aminotransferase, ++alanine aminotransferase and lactate dehydrogenase and the changes were confirmed by his topathology. Nitrendipine, nimodipine and nisoldipine (10 mg/kg, ip) significantly reduced the elevated levels of these enzymes. The average degree of cardiac necrosis in these rats when observed microscopically and histologically was also found to be significantly reduced on pretreatment with these drugs. Nisoldipine was more effective in preventing cardiac necrosis as compared to nitrendipine and nimodipine.


Subject(s)
Animals , Aspartate Aminotransferases/blood , Calcium Channel Blockers/pharmacology , Female , Heart/drug effects , Isoproterenol/toxicity , L-Lactate Dehydrogenase/blood , Male , Myocardial Infarction/drug therapy , Myocardium/pathology , Nimodipine/pharmacology , Nisoldipine/pharmacology , Nitrendipine/pharmacology , Rats
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