Normalization of lens protein kinase Cγ in galactosemic dogs by a novel aldose reductase inhibitor.

The purpose of this study was to determine the effects of a novel aldose reductase inhibitor on lens protein kinase Cγ (PKCγ) levels in galactosemic dogs. Six-month old Beagles (12 total; 6 male and 6 female) were made galactosemic by feeding a diet of 40% galactose for 6 weeks. Three dogs per group were fed either control, normal diet, 40% galactose diet, 40% galactose diet with aldose reductase inhibitor at 100 mg/kg body weight per day given orally, or a control diet with aldose reductase inhibitor alone (1-H,7-H-5α,6,8,9-tetrahydro-1-oxopyran[4,3-β]¹ benzopyran, referred to herein as HAR-1). Lenses were removed and analyzed for toxicity by pathological examination. Lens polyol concentrations were determined by GC/MS. PKCγ levels were determined by Western blot and by reverse transcriptase-polymerase chain reaction (RT-PCR). No toxicity was observed from the aldose reductase inhibitor when given at 100 mg/kg body weight per day for 6 weeks. Galactosemic dogs showed deterioration of lens cells. Deterioration included vacuole formation in the lens, cell lysis, and loss of cell nuclei. Galactosemic dogs given the HAR-1 appeared identical to control dogs. Polyol concentrations in the lenses were reduced by 50% in dogs fed the 40% galactose diet with the aldose reductase inhibitor, HAR-1. PKCγ protein levels were reduced in the galactosemic dog lenses, but synthesis of PKCγ was not affected, as measured by RT-PCR. The PKCγ protein levels were similar to controls in dogs given the aldose reductase inhibitor, HAR-1, even when polyol concentrations remained 50% elevated above control levels. HAR-1, when given to control dogs, caused a reduction in the synthesis of PKCγ mRNA but not in total PKCγ protein levels. This study demonstrates the use of a novel aldose reductase inhibitor to control changes in PKCγ in dog lens, a PKC that is known to control gap junction activity. [ABSTRACT FROM AUTHOR]