نتایج جستجو برای: amylase inhibitor

تعداد نتایج: 221351  

2012
Mi Hwa Park Ji Sook Han

This study investigated the hypoglycemic effect of the Padina arborescens extract in STZ-induced diabetic mice. Freeze-dried Padina arborescens were extracted with 80% methanol and concentrated for use in this study. The hypoglycemic effect was determined by inhibitory activities against α-glucosidase and α-amylase as well as the alleviation of postprandial blood glucose level. Padina arboresce...

Journal: :The American journal of physiology 1998
Nisha J D'Silva Kerry L Jacobson Sabrina M Ott Eileen L Watson

Rap1 has recently been identified on the secretory granule membrane and plasma membrane of rat parotid acinar cells (N. J. D'Silva, D. DiJulio, C. B. Belton, K. L. Jacobson, and E. L. Watson. J. Histochem. Cytochem. 45: 965-973, 1997). In the present study, we examined the cellular redistribution of Rap1 following treatment of acini with isoproterenol (ISO), the β-adrenergic agonist, and determ...

2014
Arumugam Madeswaran Kuppusamy Asokkumar Muthuswamy Umamaheswari Thirumalaisamy Sivashanmugam

The current objective of the study is to evaluate the α-amylase inhibitory activity of butein and tricetin using in silico docking studies. In this perspective, butein and tricetin ligands were prepared for the docking evaluation. Acarbose, a known α-amylase inhibitor was used as the standard. In silico docking studies were carried out using recent version of AutoDock 4.2, which has the basic p...

Journal: :Clinical chemistry 1991
A Abe T Nishimura A Noma K Hamano

We evaluated the enzymic mechanism by which 3-keto butylidene-beta-2-chloro-4-nitrophenyl maltopentaoside (3KB-G5-CNP) serves as a substrate for serum pancreatic (p-) and salivary (s-) amylases. In aliquots of the reaction mixture, three kinds of beta-2-chloro-4-nitrophenyl oligosaccharides (glucose, maltoside, and maltotrioside) were separated from the substrate by high-performance liquid chro...

1998
NISHA J. D’SILVA KERRY L. JACOBSON SABRINA M. OTT Kerry L. Jacobson Sabrina M. Ott

D’Silva, Nisha J., Kerry L. Jacobson, Sabrina M. Ott, and Eileen L. Watson. b-Adrenergic-induced cytosolic redistribution of Rap1 in rat parotid acini: role in secretion. Am. J. Physiol. 274 (Cell Physiol. 43): C1667–C1673, 1998.—Rap1 has recently been identified on the secretory granule membrane and plasma membrane of rat parotid acinar cells (N. J. D’Silva, D. DiJulio, C. B. Belton, K. L. Jac...

2011
Dibu Divakaran Aswathi Chandran R Pratap Chandran

Alpha amylase (α-1, 4-glucan-glucanhydrolase, EC 3.2.1.1), an extracellular enzyme, degrades α, 1-4 glucosidic linkages of starch and related substrates in an endo-fashion producing oligosaccharides including maltose, glucose and alpha limit dextrin (7). The present study deals with the production and comparative study of production of α-amylase from two strains of Bacillus licheniformis, MTCC ...

Journal: :The American journal of physiology 1998
Stefan W Schmid Irvin M Modlin Laura H Tang Aubry Stoch Steve Rhee Michael H Nathanson George A Scheele Fred S Gorelick

To identify the muscarinic subtype present on the rat pancreatic acinar cell, we examined the effects of different muscarinic receptor antagonists on amylase secretion and proteolytic zymogen processing in isolated rat pancreatic acini. Maximal zymogen processing required a concentration of carbachol 10- to 100-fold greater (10-3 M) than that required for maximal amylase secretion (10-5 M). Alt...

2012
Fernando Álvarez-Alfageme Christoph Lüthi Jörg Romeis

Genetically modified (GM) legumes expressing the α-amylase inhibitor 1 (αAI-1) from Phaseolus vulgaris L. or cysteine protease inhibitors are resistant to several bruchid pests (Coleoptera: Chrysomelidae). In addition, the combination of plant resistance factors together with hymenopteran parasitoids can substantially increase the bruchid control provided by the resistance alone. If the strateg...

2013
Weiwen Ning Yongjun Wang Fan Zhang Hengyun Wang Fan Wang Xiaojuan Wang Huaxin Tang Songping Liang Xiaoliu Shi Zhonghua Liu

HWTI is a 55-residue protein isolated from the venom of the spider Ornithoctonus huwena. It is a potent trypsin inhibitor and a moderate voltage-gated potassium channel blocker. Here, we designed and expressed two HWTI mutants, HWTI-mut1 and HWTI-mut2, in which the potassium channel inhibitory activity was reduced while the trypsin inhibitory activity of the wild type form (approximately 5 EPU/...

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