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GPR75 信号通路的激活有助于 20-HETE 类似物 5,14-HEDGE 预防脂多糖诱导的脓毒性休克大鼠模型中低血压和心动过速反应的作用。

Activation of GPR75 Signaling Pathway Contributes to the Effect of a 20-HETE Mimetic, 5,14-HEDGE, to Prevent Hypotensive and Tachycardic Responses to Lipopolysaccharide in a Rat Model of Septic Shock.

机构信息

Department of Pharmacology, Faculty of Pharmacy, Mersin University, Mersin, Turkey.

Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX ; and.

出版信息

J Cardiovasc Pharmacol. 2022 Aug 1;80(2):276-293. doi: 10.1097/FJC.0000000000001265.

Abstract

The orphan receptor, G protein-coupled receptor (GPR) 75, which has been shown to mediate various effects of 20-hydroxyeicosatetraenoic acid (20-HETE), is considered as a therapeutic target in the treatment of cardiovascular diseases in which changes in the production of 20-HETE play a key role in their pathogenesis. Our previous studies showed that 20-HETE mimetic, N -(20-hydroxyeicosa-5[Z],14[Z]-dienoyl)glycine (5,14-HEDGE), protects against vascular hyporeactivity, hypotension, tachycardia, and arterial inflammation induced by lipopolysaccharide (LPS) in rats. This study tested the hypothesis that the GPR75 signaling pathway mediates these effects of 5,14-HEDGE in response to systemic exposure to LPS. Mean arterial pressure reduced by 33 mm Hg, and heart rate increased by 102 beats/min at 4 hours following LPS injection. Coimmunoprecipitation studies demonstrated that (1) the dissociation of GPR75/Gα q/11 and GPR kinase interactor 1 (GIT1)/protein kinase C (PKC) α, the association of GPR75/GIT1, large conductance voltage and calcium-activated potassium subunit β (MaxiKβ)/PKCα, MaxiKβ/proto-oncogene tyrosine-protein kinase (c-Src), and epidermal growth factor receptor (EGFR)/c-Src, MaxiKβ, and EGFR tyrosine phosphorylation were decreased, and (2) the association of GIT1/c-Src was increased in the arterial tissues of rats treated with LPS. The LPS-induced changes were prevented by 5,14-HEDGE. N -[20-Hydroxyeicosa-6( Z ),15( Z )-dienoyl]glycine, a 20-HETE antagonist, reversed the effects of 5,14-HEDGE in the arterial tissues of LPS-treated rats. Thus, similar to 20-HETE, by binding to GPR75 and activating the Gα q/11 /PKCα/MaxiKβ, GIT1/PKCα/MaxiKβ, GIT1/c-Src/MaxiKβ, and GIT1/c-Src/EGFR signaling pathways, 5,14-HEDGE may exert its protective effects against LPS-induced hypotension and tachycardia associated with vascular hyporeactivity and arterial inflammation.

摘要

孤儿受体 G 蛋白偶联受体 (GPR)75 被证明可以介导 20-羟二十碳四烯酸 (20-HETE) 的各种作用,被认为是治疗心血管疾病的治疗靶点,其中 20-HETE 的产生变化在其发病机制中起着关键作用。我们之前的研究表明,20-HETE 类似物 N-(20-羟二十碳五烯酸-5[Z],14[Z]-二烯酰基)甘氨酸 (5,14-HEDGE) 可预防脂多糖 (LPS) 诱导的大鼠血管低反应性、低血压、心动过速和动脉炎症。本研究测试了以下假设:GPR75 信号通路介导了 5,14-HEDGE 对 LPS 全身暴露的这些作用。LPS 注射后 4 小时,平均动脉压降低 33mmHg,心率增加 102 次/分钟。共免疫沉淀研究表明:(1) GPR75/Gαq/11 和 GPR 激酶相互作用蛋白 1(GIT1)/蛋白激酶 C( PKC)α的解离、GPR75/GIT1 的结合、大电导电压和钙激活钾亚基β (MaxiKβ)/PKCα、MaxiKβ/原癌基因酪氨酸蛋白激酶(c-Src)和表皮生长因子受体(EGFR)/c-Src、MaxiKβ 和 EGFR 酪氨酸磷酸化减少,(2) 动脉组织中 GIT1/c-Src 的结合增加在 LPS 处理的大鼠中。5,14-HEDGE 可预防 LPS 诱导的变化。20-HETE 拮抗剂 N-[20-羟二十碳六烯酸-6(Z),15(Z)-二烯酰基]甘氨酸逆转了 LPS 处理大鼠动脉组织中 5,14-HEDGE 的作用。因此,与 20-HETE 类似,通过与 GPR75 结合并激活 Gαq/11/ PKCα/MaxiKβ、GIT1/ PKCα/MaxiKβ、GIT1/c-Src/MaxiKβ 和 GIT1/c-Src/EGFR 信号通路,5,14-HEDGE 可能发挥其对 LPS 诱导的低血压和心动过速的保护作用,这些作用与血管低反应性和动脉炎症有关。

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