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Publication : Conophylline inhibits non-alcoholic steatohepatitis in mice.

First Author  Nakade Y Year  2017
Journal  PLoS One Volume  12
Issue  6 Pages  e0178436
PubMed ID  28594915 Mgi Jnum  J:245453
Mgi Id  MGI:5916065 Doi  10.1371/journal.pone.0178436
Citation  Nakade Y, et al. (2017) Conophylline inhibits non-alcoholic steatohepatitis in mice. PLoS One 12(6):e0178436
abstractText  Conophylline (CnP), a vinca alkaloid extracted from the leaves of the tropical plant Ervatamia microphylla, attenuates hepatic fibrosis in mice. However, little is known about whether CnP inhibits steatosis, inflammation, and fibrosis in non-alcoholic steatohepatitis (NASH) in mice. A methionine-choline-deficient (MCD) diet was administered to male db/db mice as a NASH model, and CnP (1 mug/kg/d) was co-administered. Eight weeks after the commencement of the MCD diet, hepatic steatosis, inflammation, and fibrosis, and hepatic fat metabolism-, inflammation-, and fibrosis-related markers were examined. Feeding on an MCD for 8 weeks induced hepatic steatosis, inflammation, and fibrosis. CnP significantly attenuated the MCD-induced increases in hepatic steatosis, as well as hepatic inflammation and fibrosis. The MCD diet increased hepatic transforming growth factor-beta (TGF-beta) mRNA levels, which are correlated with hepatic steatosis, inflammation, and fibrosis. The diet also attenuated acyl-coenzyme A oxidase 1 (ACOX1) and carnitine palmitoyltransferase 1 (CPT1) mRNA levels, which are involved in beta-oxidation. The putative mechanism of the CnP effect involves reduced hepatic TGF-beta mRNA levels, and increased mRNA levels of hepatic peroxisome proliferator-activated receptor (PPAR) alpha and its target genes ACOX1 and CPT1. The results of this study indicate that CnP inhibits steatohepatitis, possibly through the inhibition of hepatic TGF-beta mRNA levels, and induces an increase in PPARalpha mRNA levels, resulting in the attenuation of hepatic steatosis, inflammation, and fibrosis in mice. CnP might accordingly be a suitable therapeutic option for NASH.
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