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Benfotiamine a synthetic S-acyl thiamine derivative has different mechanisms of action and a different pharmacological profile than lipid-soluble thiamine disulfide derivatives

机译:合成的S-酰基硫胺素Benfotiamine与脂溶性硫胺素二硫化物衍生物具有不同的作用机理和不同的药理特性

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摘要

BackgroundLipid-soluble thiamine precursors have a much higher bioavailability than genuine thiamine and therefore are more suitable for therapeutic purposes. Benfotiamine (S-benzoylthiamine O-monophosphate), an amphiphilic S-acyl thiamine derivative, prevents the progression of diabetic complications, probably by increasing tissue levels of thiamine diphosphate and so enhancing transketolase activity. As the brain is particularly sensitive to thiamine deficiency, we wanted to test whether intracellular thiamine and thiamine phosphate levels are increased in the brain after oral benfotiamine administration.
机译:背景技术脂溶性硫胺素前体的生物利用度比真正的硫胺素高得多,因此更适合用于治疗目的。两性的S-酰基硫胺素衍生物Benfotiamine(S-苯甲酰硫胺素O-单磷酸酯)可通过增加组织中的硫胺素二磷酸酯水平并因此增强转酮醇酶活性来预防糖尿病并发症的发展。由于大脑对硫胺素缺乏症特别敏感,因此我们想测试口服苯甲硫胺后大脑中细胞内硫胺素和硫胺素磷酸盐的水平是否增加。

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