Oleoylethanolamide (OEA) is an endogenous peroxisome proliferator-activated receptor alpha (PPAR-α) agonist. It is a naturally occurring ethanolamide lipid that regulates feeding and body weight in vertebrates ranging from mice to pythons.

2021年6月2日 · OEA increased the levels of proinflammatory cytokines, such as IL-6, IL-8, and IL-33, in A549 cells. In addition, it also induced eosinophilic inflammation, the production of IL-4, IL-5, IL-13,...

OEA (10 mg/kg/day) was administered orally for 8 weeks. The results showed that OEA prevented oxidative stress and endothelial cell damage, and inhibited early atherosclerotic plaque formation. 49 Table 3 summarized the results of studies regarding OEA supplementation on the inflammatory biomarkers and oxidative stress. Table 3.

原本我打算使用NAS来进行测试，但刷公众号偶然看到了网心云公众号推送的 OEA设备，价格也只是一百多。 我决定试试水，就算每天只赚一块钱，也不到半年的时间就能收回成本。 ⽽且每个账号首台可享坐享其成活动，在线达标180天包回本，所以我决定直接购买并进行测试，不再多言，直接上手试用。 相比使用NAS部署，OEA设备并不大，占用空间更小。 轻量化的好处在于你可以将其放置在电箱或鞋柜中，这样就不会有繁琐的线缆，也看不到设备本身。 平时可以直接 …

2025年2月7日 · Oleoylethanolamide (OEA) has garnered attention for its role in human biology. This lipid molecule is being studied for its impact on physiological processes related to metabolism and appetite regulation. Understanding OEA’s functions could offer insights into novel therapeutic strategies for metabolic disorders.

2021年6月2日 · Oleoylethanolamide (OEA), an endocannabinoid similar to those found in cannabis, occurs naturally in the body, and has now been implicated in promoting symptoms of asthma. OEA activates white blood cells called eosinophils and ILC2 cells, which are both parts of our immune response.

Oleoylethanolamide (OEA)可以显着抑制促纤维化细胞因子TGF-β1在肝纤维化小鼠模型中负调节TGF-β1信号通路 (α-SMA,胶原蛋白1a和胶原蛋白3a)中的基因。 用Oleoylethanolamide (5 mg/kg /天,腹腔注射,ip)治疗通过阻断肝星状细胞 (HSC)的活化,显着减弱了两种实验动物模型中肝纤维化的进展 [1]。 CFSC，HSC细胞系首先从肝硬化大鼠肝脏获得，并且具有与早期传代原代HSC相似的表型。 CFSC细胞在补充有10％胎牛血清（FBS）和1％青霉素/链霉素的Dulbecco改良 …

油酰单乙醇胺是过氧化物酶体增殖物激活受体α (PPAR- α)的激动剂。 N-油酰乙醇酰胺产生肠道信号，刺激中枢多巴胺活动，在热量-自我平衡和快乐-自我平衡之间建立联系。 油酰乙醇酰胺被认为是胃旁路手术成功的分子机制。 N-油酰乙醇酰胺是一种选择性GPR55激动剂。 Oleoylethanolamide 是一种高亲和力的内源性 PPAR-α 激动剂，可用于肥胖和动脉硬化的相关研究。 Oleoylethanolamide (OEA), an endogenous PPAR-α ligand, attenuates liver fibrosis …

Oleoylethanolamide (OEA), an endogenous PPAR-α ligand, attenuates liver fibrosis targeting hepatic stellate cells. Oleoylethanolamide suppresses TGF-β1 induced hepatic stellate cells (HSCs) activation in vitro via PPAR-α.

油酰基乙醇酰胺（oea）是一种在大脑组织和巧克力中发现的内源 性大麻素AEA的类似物。 它是长链脂肪酸乙醇酰胺在梗死组织中迅速积累的一种，但其在食物脱除后的肠内生