Acarbose — Alpha-glucosidase inhibitor (AGI) — FDA-approved antidiabetic agent with ITP-confirmed longevity activity

Acarbose is a pseudo-tetrasaccharide that competitively inhibits intestinal alpha-glucosidases (maltase, sucrase, glucoamylase, glucan-1,4-alpha-glucosidase) and pancreatic alpha-amylase. This delays and reduces the breakdown and absorption of dietary complex carbohydrates, blunting postprandial glucose spikes without increasing insulin secretion. Longevity mechanisms: (1) NIA Interventions Testing Program (ITP) — one of the most reproducible mouse longevity interventions: significant lifespan extension in male mice (+22% median lifespan in males, +5% in females in 3 independent sites); female benefit attenuated because mice consume more food due to acarbose's caloric restriction-like intestinal effect; (2) Caloric restriction mimetic mechanism — by reducing postprandial glucose, acarbose reduces AGE formation, insulin/IGF-1 signaling, and activates AMPK; (3) Gut microbiome modulation — increases production of short-chain fatty acids (propionate, butyrate) via fermentation of unabsorbed carbohydrates; (4) Reduces postprandial insulin spikes, which may extend AMPK activation periods between meals.

نظرة عامة

هذه الصفحة جزء من مكتبة المركّبات المُصنَّفة بالأدلة في Hormonaly. جميع الادعاءات السريرية مرتبطة بمصادر علمية مُحكَّمة عبر خط أنابيب التحقق المزدوج للاستشهادات.

فئة المركّب

Alpha-glucosidase inhibitor (AGI) — FDA-approved antidiabetic agent with ITP-confirmed longevity activity

آلية العمل

Acarbose is a pseudo-tetrasaccharide that competitively inhibits intestinal alpha-glucosidases (maltase, sucrase, glucoamylase, glucan-1,4-alpha-glucosidase) and pancreatic alpha-amylase. This delays and reduces the breakdown and absorption of dietary complex carbohydrates, blunting postprandial glucose spikes without increasing insulin secretion. Longevity mechanisms: (1) NIA Interventions Testing Program (ITP) — one of the most reproducible mouse longevity interventions: significant lifespan extension in male mice (+22% median lifespan in males, +5% in females in 3 independent sites); female benefit attenuated because mice consume more food due to acarbose's caloric restriction-like intestinal effect; (2) Caloric restriction mimetic mechanism — by reducing postprandial glucose, acarbose reduces AGE formation, insulin/IGF-1 signaling, and activates AMPK; (3) Gut microbiome modulation — increases production of short-chain fatty acids (propionate, butyrate) via fermentation of unabsorbed carbohydrates; (4) Reduces postprandial insulin spikes, which may extend AMPK activation periods between meals.

الوضع التنظيمي

FDA APPROVED for Type 2 Diabetes (adjunct to diet and exercise). All longevity use is OFF-LABEL. Generic drug; very inexpensive.

مستوى الأدلة

B — FDA-approved T2D drug with RCT data (STOP-NIDDM trial, n=1,429: prevented T2D progression in 25% of cases and reduced MI by 35%). ITP lifespan studies: 3 independent sites confirmed +22% male median lifespan extension at 1000 ppm in chow (Harrison et al., 2014, 2019). No completed human longevity RCT.