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USE OF INHIBITORS OF PHOSPHATASE ACTIVITY OF SOLUBLE EPOXIDE FOR THE TREATMENT OF CARDIOMETABOLIC DISEASES

机译:可溶性环氧化物的磷酸酶活性的抑制剂用于治疗心细素疾病

摘要

The growing prevalence of obesity and type 2 diabetes complicates risk and clinical management by potentiating and/or exacerbating hypertension, hyperlipidemia, atherosclerosis and cardiomyopathy, leading to increasing use of the term “cardiometabolic disease” (CMD) to encompass the many facets of this complex syndrome. The inventors assessed the role of the soluble epoxide hydrolase (she) phosphatase domain in metabolism and cardiovascular system, by generating sEH phosphatase knock-in (KI) animals (rats). They unexpectedly revealed that inhibition of the phosphatase domain of sEH improves cardiac systolic function, decreases body weight and increases insulin sensitivity. Moreover under high fat diet, the animals have a decreased body weight gain, were protected against the development of insulin resistance, hepatic steatosis and cardiac hypertrophy. Inhibition of the phosphatase domain of sEH thus represents a new pharmacological target in the treatment of cardiometabolic diseases.
机译:肥胖症和2型糖尿病的患病率不变,通过增强和/或加剧高血压,高脂血症,动脉粥样硬化和心肌病,导致使用术语“心细素疾病”(CMD)的使用来使风险和临床管理变得使风险和临床管理变得使风险和临床管理变得越来越多,以包括这种复杂的许多方面综合征。发明人通过产生SEH磷酸酶敲入(KI)动物(大鼠)来评估可溶性环氧化物水解酶(SHE)磷酸酶磷酸酶域在代谢和心血管系统中的作用。它们意外地揭示了SEH的磷酸酶结构域的抑制改善了心脏收缩功能,降低了体重并增加了胰岛素敏感性。此外,在高脂肪饮食中,动物体重增加减少,受到胰岛素抵抗,肝脏脂肪变性和心脏肥大的发展。因此,SEH的磷酸酶结构域的抑制是治疗心细素疾病的新药理学靶标。

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