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1.
Indian J Exp Biol ; 1994 Sep; 32(9): 612-5
Article in English | IMSEAR | ID: sea-56782

ABSTRACT

Isatin (15-25 mM) inhibited rat brush border sucrase by 40% in presence of Na+ and the inhibition was enhanced to over 60% in sodium free medium. Sucrase inhibition by isatin was dependent on pH. Kinetic analysis revealed a pure capacity type (Vmax-effect) inhibition of sucrase activity by isatin in presence of sodium. But it changed to affinity type (K-effect) in sodium free medium. The value of Ki was around 20-25 mM under these conditions. Enzyme inhibition by isatin was alleviated by increasing Na+ or sucrose concentrations. Other monovalent cations like K+, Li+ and Cs+ were also effective in restoring the enzyme activity to control levels. The effectiveness of the metal ions in alleviating the enzyme inhibition was in the order of Na+ > Cs+ > K+ > Li+.


Subject(s)
Animals , Intestine, Small/drug effects , Isatin/pharmacology , Male , Microvilli/drug effects , Rats , Rats, Wistar , Sucrase/antagonists & inhibitors
2.
Indian J Biochem Biophys ; 1994 Jun; 31(3): 191-4
Article in English | IMSEAR | ID: sea-27425

ABSTRACT

Isatin (10 mM) inhibited the activity of rabbit brush border sucrase by 60% at pH 5.0 but it had no effect on enzyme activity around neutral pH. Isatin inhibition of sucrase was unaffected by Na+ ions but K+ and Cs+ ions reduced enzyme inhibition, partially. Kinetic analysis revealed that sucrase inhibition by isatin at acidic pH was non-competitive with Ki of the order 6.5-7.8 mM. Isatin together with 4 mM harmaline or iodoacetate (3 mM) or dithionitrobenzene (2 mM) yielded 80-85% inhibition of the enzyme. These observations suggest that inhibitory sites for isatin, harmaline and -SH group reacting agents are distinct in rabbit brush border sucrase.


Subject(s)
Animals , Hydrogen-Ion Concentration , Intestines/enzymology , Isatin/metabolism , Microvilli/enzymology , Rabbits , Sucrase/antagonists & inhibitors
3.
Indian J Physiol Pharmacol ; 1975 Apr-Jun; 19(2): 71-5
Article in English | IMSEAR | ID: sea-108085

ABSTRACT

Studies have been done on the effect of Penicillin, Streptomycin and Isonicotinic Acid hydrazide on small intestinal oligosaccharidase and it was observed that the drug penicillin inhibited the enzyme lactase and sucrase by 62.7% and 34.7% respectively, whereas I.N.H. inhibited the enzyme sucrase and maltase by 57.1% and 56.14% respectively. Streptomycin did not show any inhibitory effect on those enzymes. Lactose tolerance test showed impairment of lactose absorption in case of penicillin. Fasting serum sugar level was diminished both in penicillin and streptomycin and the absorption capacity was increased after oral administration of streptomycin.


Subject(s)
Animals , Blood Glucose/analysis , Depression, Chemical , Disaccharidases/antagonists & inhibitors , Galactosidases/antagonists & inhibitors , Glucosidases/antagonists & inhibitors , Intestinal Absorption/drug effects , Intestine, Small/enzymology , Isoniazid/pharmacology , Lactose/metabolism , Male , Penicillins/pharmacology , Rabbits , Rats , Streptomycin/pharmacology , Sucrase/antagonists & inhibitors
4.
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