Ja. Luo et al., Novel terpenoid-type quinones isolated from Pycnanthus angolensis of potential utility in the treatment of type 2 diabetes, J PHARM EXP, 288(2), 1999, pp. 529-534
Citations number
12
Categorie Soggetti
Pharmacology & Toxicology
Journal title
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
Using an ethnomedical-based drug discovery program, two previously unknown
compounds (SP-18904 and SP-18905) from Pycnanthus angolensis were isolated
that lower glucose concentrations in mouse models of type 2 diabetes. SP-18
904 and SP-18905 are terpenoid-type quinones that significantly lowered pla
sma glucose concentration (p < .05) when given orally to either ob/ob or db
/db mice, both of which are hyperglycemic and hyperinsulinemic. The antihyp
erglycemic actions of SP-18904 and SP-18905 were associated with significan
t decreases in plasma insulin concentrations (p < .05), suggesting that bot
h compounds lowered glucose by enhancing insulin-mediated glucose uptake. T
his was supported by the insulin suppression test in ob/ob mice. Studies in
hyperglycemic, insulin-deficient mice and in vitro experiments on 3T3-L1 a
dipocytes further supported this conclusion. As such, these two terpenoid-t
ype quinones represent a new class of compounds of potential use in the tre
atment of type 2 diabetes.