Department of Hypertension and Endocrinology, Center for Hypertension and Metabolic Diseases, Daping Hospital, Third Military Medical University, Chongqing Institute of Hypertension, Chongqing 400042, China.
Hypertension. 2014 Jun;63(6):1354-63. doi: 10.1161/HYPERTENSIONAHA.113.02573. Epub 2014 Mar 17.
Environmental cold is a nonmodifiable hypertension risk factor. Transient receptor potential melastatin subtype 8 (TRPM8) is a cold-sensing cation channel that can be activated by menthol, a compound with a naturally cold sensation in mint. Little is known about the effect of TRPM8 activation on vascular function and blood pressure. Here, we report that TRPM8 is abundantly expressed in the vasculature. TRPM8 activation by menthol attenuated vasoconstriction via RhoA/Rho kinase pathway inhibition in wild-type mice, but the effect was absent in TRPM8(-/-) mice. Chronic dietary menthol blunted mesenteric arterial constriction and lowered blood pressure in genetic hypertensive rats via inhibition of RhoA/Rho kinase expression and activity in the vivo study. TRPM8 effect was associated with inhibition of intracellular calcium release from the sarcoplasmic reticulum, RhoA/Rho kinase activity, and sustained arterial contraction in the vitro study. Importantly, 8-week chronic menthol capsule treatment moderately lowered systolic blood pressure and diastolic blood pressure in prehypertensive individuals compared with the placebo group. Furthermore, chronic menthol capsule administration also improved flow-mediated dilatation in prehypertensive individuals, but not in the placebo group. In conclusion, our study demonstrates that TRPM8 activation by menthol benefits vascular function and blood pressure by inhibiting calcium signaling-mediated RhoA/Rho kinase activation in the vasculature. These findings add to the evidence that long-term dietary menthol treatment had favorable effects on hypertension treatment.
环境寒冷是一种不可改变的高血压风险因素。瞬时受体电位 melastatin 亚家族 8(TRPM8)是一种冷敏感阳离子通道,薄荷醇可激活该通道,薄荷醇是薄荷中具有天然冷感的化合物。关于 TRPM8 激活对血管功能和血压的影响知之甚少。在这里,我们报告 TRPM8 在血管中大量表达。薄荷醇激活 TRPM8 通过抑制 RhoA/Rho 激酶通路在野生型小鼠中减弱血管收缩,但在 TRPM8(-/-)小鼠中则没有作用。在体内研究中,慢性饮食薄荷醇通过抑制 RhoA/Rho 激酶表达和活性,减弱遗传高血压大鼠肠系膜动脉收缩和降低血压。TRPM8 作用与抑制肌浆网内钙离子从肌浆网释放、RhoA/Rho 激酶活性和动脉持续收缩有关。重要的是,与安慰剂组相比,8 周慢性薄荷醇胶囊治疗可使高血压前期个体的收缩压和舒张压适度降低。此外,慢性薄荷醇胶囊给药还可改善高血压前期个体的血流介导的血管扩张,但在安慰剂组则没有。总之,我们的研究表明,薄荷醇激活 TRPM8 通过抑制钙信号转导介导的 RhoA/Rho 激酶在血管中的激活,有益于血管功能和血压。这些发现增加了长期饮食薄荷醇治疗对高血压治疗有益的证据。