Recent Developments in Alpha-Glucosidase Inhibitors for Management of Type-2 Diabetes: An Update.
Alpha-glucosidase
alpha-amylase
diabetes
hyperglycemia
insulin
pancreas.
Journal
Current pharmaceutical design
ISSN: 1873-4286
Titre abrégé: Curr Pharm Des
Pays: United Arab Emirates
ID NLM: 9602487
Informations de publication
Date de publication:
2019
2019
Historique:
received:
19
06
2019
accepted:
12
07
2019
pubmed:
25
7
2019
medline:
17
4
2020
entrez:
24
7
2019
Statut:
ppublish
Résumé
The incidence of diabetes has increased globally in recent years and figures of diabetic patients were estimated to rise up to 642 million by 2040. The disorder is accompanied with various complications if not managed at the early stages, and interlinked high mortality rate and morbidity with time. Different classes of drugs are available for the management of type 2 diabetes but were having certain limitations of their safety. Alphaglucosidase is a family of enzyme originated from the pancreas which plays a role in the anabolism of 80-90% of carbohydrate consumed into glucose. This glucose is absorbed into the blood and results in frank postprandial hyperglycemia and worsens the conditions of diabetic patients which precipitate complications. Inhibition of these enzymes helps to prevent postprandial hyperglycemia and the formation of glycated end products. Alphaglucosidase inhibitors are reported to be more important in adequate control of type 2, but marketed drugs have various side effects, such as poor patient compliance and also expensive. This proves the needs for other class of drugs with better efficacy, safety, patient compliance and economic. In this review, we have emphasized the recent advances in the field of new alpha-glucosidase inhibitors with improved safety and pharmacological profile.
Identifiants
pubmed: 31333110
pii: CPD-EPUB-99714
doi: 10.2174/1381612825666190717104547
doi:
Substances chimiques
Blood Glucose
0
Glycoside Hydrolase Inhibitors
0
Hypoglycemic Agents
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
2510-2525Informations de copyright
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