De Novo lipogenesis inhibitors: as the other innovative agents for therapy of metabolic diseases (obesity, NAFLD/NASH, CVD)

Kulvinder Kochar Kaur
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Abstract

For survival fatty acids are necessary, working as substrates for bioenergy generation, structural constitutents along with signaling molecules. With their key part, evolutionary modes bycells for fatty acids formation from alternative carbon resources via a event labelled as de novo’’ lipogenesis ( DNL). In spite of the knowledge of significance regarding its up regulation abnormalities being correlatedwith numerous types of pathological conditions. Attempt at hampering core DNL enzymes inclusive ofcitrate/iso citratecarrier(CIC), ATP citrate lyase ( ACLY), acetyl CoA carboxylase(ACC) along with fatty acid synthase( FAS) apparently should turn out to be a good therapeutic approach. Although numeroushurdles anticipated regarding effectiveness, selectiveness besides safety variable newer classes of synthetic DNL hampering agents have reached clinical stage generation besides becoming the basis for a newer class of treatment substances. Having earlier reviewed numerous articles regarding obesity along with its co-morbidities type2 Diabetes mellitus (T2DM) NAFLD /NASH here we have presented a narrative review regarding the evolutionary generation of DNL hampering agents as potential treatment agents. For this we review utilizing search engine pubmed, google scholar; web of science; embase; Cochrane review library for which we have extracted data from earliest data with the recognition of significance of various enzymes besides their allosteric, covalent, transcriptional control of fatty acids generation & the problems encountered for their generation till date. Apart from obesity associated therapeutics their utility extends to acne vulgaris, various cancer thrapies besides treating neurod generational diseases.
新生脂肪生成抑制剂:作为治疗代谢性疾病(肥胖、NAFLD/NASH、心血管疾病)的其他创新药物
脂肪酸是生存所必需的,它是生物能量产生的底物、结构成分和信号分子。它们的关键部分是细胞的进化模式,通过一种被称为“脂肪生成”(DNL)的事件,从可替代的碳资源中形成脂肪酸。尽管对其向上调节异常与许多类型的病理条件相关的重要性的认识。试图抑制核心酶,包括枸橼酸/异柠檬酸载体酶(CIC)、ATP柠檬酸裂解酶(ACLY)、乙酰辅酶a羧化酶(ACC)和脂肪酸合成酶(FAS),显然是一种很好的治疗方法。尽管预期在有效性、选择性和安全性变量方面存在许多障碍,但新型合成DNL抑制剂已进入临床阶段,并成为新型治疗物质的基础。在先前回顾了许多关于肥胖及其合并症2型糖尿病(T2DM) NAFLD /NASH的文章后,我们在此提出了一篇关于DNL抑制剂作为潜在治疗药物的进化过程的叙述性综述。为此,我们回顾了利用搜索引擎pubmed,谷歌学者;科学网;embase;我们从最早的数据中提取了Cochrane综述库的数据,并认识到各种酶在脂肪酸生成中的变构、共价、转录控制的重要性,以及迄今为止它们在生成过程中遇到的问题。除了肥胖相关的治疗外,它们的用途还扩展到寻常痤疮,各种癌症治疗以及治疗神经代际疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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