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酯型局麻药对肌浆网 Ca-ATP 酶作用的差异机制。

Differential mechanism of the effects of ester-type local anesthetics on sarcoplasmic reticulum Ca-ATPase.

机构信息

Biophysics Department, School of Dentistry, University of Buenos Aires, M T de Alvear 2142, 17th Floor B, Buenos Aires, 1122AAH, Argentina,

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2013 Dec;386(12):1061-9. doi: 10.1007/s00210-013-0907-7. Epub 2013 Aug 15.

Abstract

The effect of the local anesthetics procaine and tetracaine on sarcoplasmic reticulum membranes isolated from two masticatory muscles, masseter and medial pterygoid, was tested and compared to fast-twitch muscles. The effects of the anesthetics on Ca-ATPase activity, calcium binding, uptake, and phosphorylation of the enzyme by inorganic phosphate (Pi) were tested with radioisotopic methods. Calcium binding to the Ca-ATPase was non-competitively inhibited, and the enzymatic activity decreased in a concentration-dependent manner. The inhibition of the activity depended on pH, calcium concentration, the presence of the calcium ionophore calcimycin, and the membrane protein concentration. Unlike fast-twitch membranes, the pre-exposure of the masseter and medial pterygoid membranes to the anesthetics enhanced the enzymatic activity in the absence of calcimycin, supporting their permeabilizing effect. Procaine and tetracaine also interfered with the calcium transport capability, decreasing the maximal uptake without modification of the calcium affinity for the ATPase. Besides, the anesthetics inhibited the phosphorylation of the enzyme by Pi in a competitive manner. Tetracaine revealed a higher inhibitory potency on Ca-ATPase compared to procaine, and the inhibitory concentrations were lower than usual clinical doses. It is concluded that procaine and tetracaine not only affect key steps of the Ca-ATPase enzymatic cycle but also exert an indirect effect on membrane permeability to calcium and suggest that the consequent myoplasmic calcium increase induced by the anesthetics might account for myotoxic effects, such as sustained contraction and eventual rigidity of both fast-twitch and masticatory muscles.

摘要

局部麻醉药普鲁卡因和丁卡因对两块咀嚼肌(咬肌和翼内肌)和快肌肌浆网膜的作用进行了测试和比较。采用放射性同位素方法检测了麻醉剂对 Ca-ATP 酶活性、钙结合、酶的无机磷(Pi)摄取和磷酸化的影响。钙与 Ca-ATP 酶的结合呈非竞争性抑制,酶活性呈浓度依赖性降低。抑制活性取决于 pH 值、钙离子浓度、钙载体钙调霉素的存在以及膜蛋白浓度。与快肌膜不同,在没有钙调霉素的情况下,预先暴露于普鲁卡因和丁卡因的咬肌和翼内肌膜增强了酶的活性,支持它们的渗透作用。普鲁卡因和丁卡因还干扰了钙转运能力,在不改变钙与 ATP 酶亲和力的情况下降低了最大摄取量。此外,麻醉剂以竞争性方式抑制酶的磷酸化。与普鲁卡因相比,丁卡因对 Ca-ATP 酶的抑制作用更强,抑制浓度低于常用的临床剂量。综上所述,普鲁卡因和丁卡因不仅影响 Ca-ATP 酶酶循环的关键步骤,而且对钙向膜的通透性产生间接影响,提示麻醉剂引起的细胞浆内钙增加可能导致肌肉毒性作用,如快肌和咀嚼肌的持续收缩和最终僵硬。

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