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吡哆醇与动脉粥样硬化:在喂食含16%酪蛋白的正常及高脂、高胆固醇饮食的大鼠中,吡哆醇在脂质和糖胺聚糖代谢中的作用

Pyridoxine and atherosclerosis: role of pyridoxine in the metabolism of lipids and glycosaminoglycans in rats fed normal and high fat, high cholesterol diets containing 16% casein.

作者信息

Vijayammal P L, Kurup P A

出版信息

Aust J Biol Sci. 1978 Feb;31(1):7-20. doi: 10.1071/bi9780007.

Abstract

The effect of administration of low and high doses of pyridoxine on the metabolism of lipids and glycosaminoglycans has been studied in rats fed normal and high fat, high cholesterol diets. Low doses of pyridoxine (0.005 mg/100 g body weight) caused increased concentrations, of cholesterol and triglycerides in the serum and aorta in animals fed normal and high fat, high cholesterol diets. Administration of high doses of pyridoxine (5.0 mg/100 g body weight) caused decrease in the concentration of these lipids in these tissues except in the case of the aorta in the animals fed a normal diet. Low doses of pyridoxine generally caused a decrease in the concentration of many glycosaminoglycan fractions in the aorta in rats fed normal and high fat, high cholesterol diets, whilst high doses caused an increase. The activity of glucosaminephosphate isomerase (glutamine-forming) and UDPglucose dehydrogenase, both key enzymes in the biosynthetic pathway of glycosaminoglycans, decreased in rats given low doses of pyridoxine and increased in rats given high doses. The activity of many enzymes concerned with degradation of glycosaminoglycans--hyaluronoglucosidase, beta-glucuronidase, beta-N-acetylglucosaminidase, aryl sulphatase, and cathepsin D--generally increased in rats fed low doses of the pyridoxine and decreased in those given high doses. The concentration of hepatic 3'-phosphoadenosine-5'-phosphosulphate, and the activity of the sulphate-activating system and of aryl sulphotransferase decreased when the dose of pyridoxine was low and increased when the dose was high.

摘要

在喂食正常饮食以及高脂肪、高胆固醇饮食的大鼠中,研究了低剂量和高剂量吡哆醇给药对脂质和糖胺聚糖代谢的影响。低剂量的吡哆醇(0.005毫克/100克体重)会导致喂食正常饮食以及高脂肪、高胆固醇饮食的动物血清和主动脉中的胆固醇和甘油三酯浓度升高。高剂量的吡哆醇(5.0毫克/100克体重)给药会使这些组织中的这些脂质浓度降低,但喂食正常饮食的动物的主动脉除外。低剂量的吡哆醇通常会导致喂食正常饮食以及高脂肪、高胆固醇饮食的大鼠主动脉中许多糖胺聚糖组分的浓度降低,而高剂量则会使其升高。糖胺聚糖生物合成途径中的关键酶磷酸葡糖胺异构酶(谷氨酰胺形成型)和UDP葡萄糖脱氢酶的活性,在给予低剂量吡哆醇的大鼠中降低,而在给予高剂量的大鼠中升高。许多与糖胺聚糖降解相关的酶——透明质酸葡萄糖苷酶、β-葡萄糖醛酸酶、β-N-乙酰氨基葡萄糖苷酶、芳基硫酸酯酶和组织蛋白酶D——的活性,在喂食低剂量吡哆醇的大鼠中通常会升高,而在给予高剂量的大鼠中则会降低。当吡哆醇剂量较低时,肝脏3'-磷酸腺苷-5'-磷酸硫酸酯的浓度、硫酸盐激活系统和芳基磺基转移酶的活性会降低,而当剂量较高时则会升高。

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