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Abstract
The isolation and characterization of rat lens aldose reductase (RLAR) inhibitors from the fruiting bodies of Ganoderma applanatum were conducted. Among the extracts and fractions from G. applanatum tested, the MeOH extract and EtOAc fraction were found to exhibit potent RLAR inhibition in vitro, their IC_<50> being 1.7 and 0.8μg/ml, respectively. From the active EtOAc fraction, seven compounds with diverse structural moieties were isolated and identified as D-mannitol (1), 2-methoxyfatty acids (2), cerebrosides (3), daucosterol (4), 2,5-dihydroxyacetophenone (5), 2,5-dihydroxybenzoic acid (6), and protocatechualdehyde (7). Among them, protocatechualdehyde (7) was found to be the most potent RLAR inhibitor (IC_<50>=0.7μg/ml), and may be useful for the prevention and/or treatment of diabetic complications.
Journal
- Biological & pharmaceutical bulletin [List of Volumes]
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Biological & pharmaceutical bulletin 28(6), 1103-1105, 2005-06-01 [Table of Contents]
The Pharmaceutical Society of Japan