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健康与疾病中的花生四烯酸代谢

Arachidonic acid metabolism in health and disease.

作者信息

Zhang Yiran, Liu Yingxiang, Sun Jin, Zhang Wei, Guo Zheng, Ma Qiong

机构信息

Department of Orthopedic Surgery Orthopedic Oncology Institute The Second Affiliated Hospital of Air Force Medical University Xi'an China.

Department of Pathology The Second Affiliated Hospital of Air Force Medical University Xi'an China.

出版信息

MedComm (2020). 2023 Sep 20;4(5):e363. doi: 10.1002/mco2.363. eCollection 2023 Oct.

DOI:10.1002/mco2.363
PMID:37746665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10511835/
Abstract

Arachidonic acid (AA), an n-6 essential fatty acid, is a major component of mammalian cells and can be released by phospholipase A2. Accumulating evidence indicates that AA plays essential biochemical roles, as it is the direct precursor of bioactive lipid metabolites of eicosanoids such as prostaglandins, leukotrienes, and epoxyeicosatrienoic acid obtained from three distinct enzymatic metabolic pathways: the cyclooxygenase pathway, lipoxygenase pathway, and cytochrome P450 pathway. AA metabolism is involved not only in cell differentiation, tissue development, and organ function but also in the progression of diseases, such as hepatic fibrosis, neurodegeneration, obesity, diabetes, and cancers. These eicosanoids are generally considered proinflammatory molecules, as they can trigger oxidative stress and stimulate the immune response. Therefore, interventions in AA metabolic pathways are effective ways to manage inflammatory-related diseases in the clinic. Currently, inhibitors targeting enzymes related to AA metabolic pathways are an important area of drug discovery. Moreover, many advances have also been made in clinical studies of AA metabolic inhibitors in combination with chemotherapy and immunotherapy. Herein, we review the discovery of AA and focus on AA metabolism in relation to health and diseases. Furthermore, inhibitors targeting AA metabolism are summarized, and potential clinical applications are discussed.

摘要

花生四烯酸(AA)是一种n-6必需脂肪酸,是哺乳动物细胞的主要成分,可由磷脂酶A2释放。越来越多的证据表明,AA起着重要的生化作用,因为它是前列腺素、白三烯和环氧二十碳三烯酸等类花生酸生物活性脂质代谢产物的直接前体,这些产物可通过三种不同的酶促代谢途径获得:环氧化酶途径、脂氧合酶途径和细胞色素P450途径。AA代谢不仅参与细胞分化、组织发育和器官功能,还参与疾病的进展,如肝纤维化、神经退行性变、肥胖、糖尿病和癌症。这些类花生酸通常被认为是促炎分子,因为它们可以引发氧化应激并刺激免疫反应。因此,干预AA代谢途径是临床上治疗炎症相关疾病的有效方法。目前,靶向AA代谢途径相关酶的抑制剂是药物发现的一个重要领域。此外,AA代谢抑制剂与化疗和免疫疗法联合应用的临床研究也取得了许多进展。在此,我们综述了AA的发现,并重点关注与健康和疾病相关的AA代谢。此外,总结了靶向AA代谢的抑制剂,并讨论了其潜在的临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/a7ce5109f201/MCO2-4-e363-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/99618e276f64/MCO2-4-e363-g023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/28bc5dc0141a/MCO2-4-e363-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/e51cf3da60d9/MCO2-4-e363-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/d478d9a3e0a2/MCO2-4-e363-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/b2244927ed03/MCO2-4-e363-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/a7ce5109f201/MCO2-4-e363-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/99618e276f64/MCO2-4-e363-g023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/28bc5dc0141a/MCO2-4-e363-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/e51cf3da60d9/MCO2-4-e363-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/d478d9a3e0a2/MCO2-4-e363-g016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/b2244927ed03/MCO2-4-e363-g017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ab/10511835/a7ce5109f201/MCO2-4-e363-g011.jpg

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