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MTP阻害薬およびACAT阻害薬の最新動向

机译:MTP和ACAT抑制剂的最新趋势

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Currently, statin therapy is the first-line treatment for patients with hypercholesterole-mia, although their effects on plasma triglyceride (TG) levels are modest and variable. Inhibition of microsomal triglyceride transfer protein (MTP), a key protein involved in the assembly of the apoB-containing lipoproteins, is an attractive lipid-lowering strategy. In animal models, MTP inhibitors have dramatic effects not only on plasma cholesterol and LDL levels but on TG levels as well, offering the potential for greater efficacy and plasma lipid control in both hypertriglyceridemia and mixed hyperlipidemia. Inhibitors of acyl-CoA: cholesterol acyltransferase(ACAT) present another strategy in treating atherosclerosis through direct inhibition of ACAT in macrophages of the arterial wall. Recent studies in mouse models of atherosclerosis lacking ACAT1, however, may argue against the selective inhibition of macrophage ACAT1.
机译:目前,尽管他汀类药物对血浆甘油三酸酯(TG)水平的影响适中且变化多端,但他汀类药物治疗仍是高胆固醇血症患者的一线治疗。抑制微粒体甘油三酸酯转移蛋白(MTP)是一种有吸引力的降脂策略,该蛋白是包含apoB的脂蛋白组装中的关键蛋白。在动物模型中,MTP抑制剂不仅对血浆胆固醇和LDL水平有显着影响,而且对TG水平也有显着影响,在高甘油三酯血症和混合性高脂血症中都具有更高的疗效和血浆脂质控制的潜力。酰基辅酶A的抑制剂:胆固醇酰基转移酶(ACAT)通过直接抑制动脉壁巨噬细胞中的ACAT,提出了另一种治疗动脉粥样硬化的策略。然而,在缺乏ACAT1的动脉粥样硬化小鼠模型中的最新研究可能反对巨噬细胞ACAT1的选择性抑制。

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