Zhao Yejun, Sun Lena
Department of Anesthesiology, College of Physicians and Surgeons, Columbia University, New York, USA.
J Clin Neurosci. 2008 Nov;15(11):1264-9. doi: 10.1016/j.jocn.2007.11.007. Epub 2008 Sep 23.
Norepinephrine transporter (NET) and serotonin transporter (SERT) proteins regulate norepinephrine (NE) and serotonin via their reuptake function and are targets of antidepressants action. Several intravenous (IV) anesthetics have been shown to inhibit NET and SERT. The interactions between antidepressants and anesthetics on transporter function, however, are not well studied. We examined the effect of different IV anesthetics on NET and SERT function, with and without chronic antidepressant pretreatment, by measuring NE or 5-hydroxytryptamine (5-HT) uptake and determined NET and SERT protein expression via immunoblotting. Both ketamine and propofol inhibited NET dose-dependently (propofol 10(-4)M -22%+/-5.6%, and propofol 10(-3)M -35%+/-5.7%; ketamine 10(-4)M -23%+/-4.1% and ketamine 10(-3)M -73%+/-2.9%); and SERT (propofol 10(-4)M -11%+/-4.3% and propofol 10(-3)M -23%+/-3.8%; ketamine 10(-4)M -29%+/-5.2% and ketamine 10(-3)M -63%+/-6.4%). Etomidate and thiopental had no effect on either NET or SERT function. Desipramine and fluoxetine, specific inhibitors of NET and SERT, respectively, both enhanced the inhibitory effects of propofol but reduced the inhibitory effects of ketamine on NET and SERT functions. IV anesthetics treatment did not change transporter protein expression in the presence of its respective inhibitor. Our results demonstrate that both ketamine and propofol inhibited SERT and NET function, but the inhibition was differentially modulated by antidepressants. Therefore, in the clinical context, this would suggest that patients receiving antidepressant treatments might have altered response to IV anesthetics in an agent-specific manner.
去甲肾上腺素转运体(NET)和5-羟色胺转运体(SERT)蛋白通过其再摄取功能调节去甲肾上腺素(NE)和5-羟色胺,并且是抗抑郁药作用的靶点。已有研究表明,几种静脉麻醉药可抑制NET和SERT。然而,抗抑郁药与麻醉药对转运体功能的相互作用尚未得到充分研究。我们通过测量NE或5-羟色胺(5-HT)摄取,研究了不同静脉麻醉药在有无慢性抗抑郁药预处理情况下对NET和SERT功能的影响,并通过免疫印迹法测定NET和SERT蛋白表达。氯胺酮和丙泊酚均呈剂量依赖性抑制NET(丙泊酚10⁻⁴M -22%±5.6%,丙泊酚10⁻³M -35%±5.7%;氯胺酮10⁻⁴M -23%±4.1%,氯胺酮10⁻³M -73%±2.9%);以及SERT(丙泊酚10⁻⁴M -11%±4.3%,丙泊酚10⁻³M -23%±3.8%;氯胺酮10⁻⁴M -29%±5.2%,氯胺酮10⁻³M -63%±6.4%)。依托咪酯和硫喷妥钠对NET或SERT功能均无影响。地昔帕明和氟西汀分别为NET和SERT的特异性抑制剂,二者均增强了丙泊酚的抑制作用,但降低了氯胺酮对NET和SERT功能的抑制作用。在存在各自抑制剂的情况下,静脉麻醉药治疗未改变转运体蛋白表达。我们的结果表明,氯胺酮和丙泊酚均抑制SERT和NET功能,但抗抑郁药对这种抑制作用有不同的调节。因此,在临床情况下,这表明接受抗抑郁治疗的患者可能会以药物特异性方式改变对静脉麻醉药的反应。