Lipid analysis in bovine lens parts after in vitro incubation in the presence of an HMG-CoA-reductase inhibitor.

Lens and eye toxicity research Pub Date : 1990-01-01
U Murawski, O Hockwin
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Abstract

Normal bovine lenses and bovine lenses after incubation in TC 199 in the presence of a lipid lowering drug were divided into four parts: the equatorial ring, the nucleus, the anterior cortex and posterior cortex. The lipids were extracted according to Egge et al. (1). Total lipids were determined gravimetrically, the lipid fractions phospholipids (PL), cardiolipin (CL), free fatty acids (FFA) and cholesterol (CH) were separated by thin layer chromatography and determined quantitative by densitometry after charring with 10% sulfuric acid. There are differences in lipid distribution between the four lens compartments, but there are no differences between normal and drug treated lenses in total lipids and lipid fractions. This result could be explained in different ways: either during this incubation time of 24 hours at 37 degrees C there will be no effect on the lens epithelial cells or there is no de-novo synthesis of lipids, especially of cholesterol in the bovine lens epithelium which could be influenced by lipid lowering drugs like HMG-CoA reductase inhibitors.

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在hmg -辅酶a还原酶抑制剂的存在下,体外培养后牛晶状体部分的脂质分析。
将正常牛晶体和经降脂药物在TC 199中孵育后的牛晶体分为四部分:赤道环、核、前皮层和后皮层。脂质提取方法参照Egge等(1),用重量法测定总脂质,脂质组分磷脂(PL)、心磷脂(CL)、游离脂肪酸(FFA)和胆固醇(CH)用薄层色谱分离,10%硫酸炭化后密度法定量测定。四个晶状体隔室之间的脂质分布存在差异,但正常晶状体和药物处理晶状体的总脂质和脂质分数没有差异。这一结果可能有不同的解释:在37摄氏度的24小时孵育时间内,对晶状体上皮细胞没有影响,或者脂质没有重新合成,尤其是牛晶状体上皮中的胆固醇,这可能受到HMG-CoA还原酶抑制剂等降脂药物的影响。
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