Kumar Manoj, González Lorie A, Dillon Glenn H
Department of Physiology and Pharmacology and Center for Neuroscience, West Virginia University School of Medicine, Robert C. Byrd Health Sciences Center, Morgantown, WV 26506, USA.
Department of Pharmacology and Neuroscience, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.
Neuropharmacology. 2015 Oct;97:414-25. doi: 10.1016/j.neuropharm.2015.04.007. Epub 2015 Apr 18.
Carisoprodol is a widely prescribed muscle relaxant, abuse of which has grown considerably in recent years. It directly activates and allosterically modulates α1β2γ2 GABAARs, although the site(s) of action are unknown. To gain insight into the actions of carisoprodol, subunit-dependent effects of this drug were assessed. Whole-cell patch clamp recordings were obtained from HEK293 cells expressing α1β2, α1β3 or αxβzγ2 (where x = 1-6 and z = 1-3) GABAARs, and in receptors incorporating the δ subunit (modeling extrasynaptic receptors). The ability to directly gate and allosterically potentiate GABA-gated currents was observed for all configurations. Presence or absence of the γ2 subunit did not affect the ability of carisoprodol to directly gate or allosterically modulate the receptor. Presence of the β1 subunit conferred highest efficacy for direct activation relative to maximum GABA currents, while presence of the β2 subunit conferred highest efficacy for allosteric modulation of the GABA response. With regard to α subunits, carisoprodol was most efficacious at enhancing the actions of GABA in receptors incorporating the α1 subunit. The ability to directly gate the receptor was generally comparable regardless of the α subunit isoform, although receptors incorporating the α3 subunit showed significantly reduced direct gating efficacy and affinity. In extrasynaptic (α1β3δ and α4β3δ) receptors, carisoprodol had greater efficacy than GABA as a direct gating agonist. In addition, carisoprodol allosterically potentiated both EC20 and saturating GABA concentrations in these receptors. In assessing voltage-dependence, we found direct gating and inhibitory effects were insensitive to membrane voltage, whereas allosteric modulatory effects were affected by membrane voltage. Our findings demonstrate direct and allosteric effects of carisoprodol at synaptic and extrasynpatic GABAARs and that subunit isoform influences these effects.
卡立普多是一种广泛使用的肌肉松弛剂,近年来其滥用现象显著增加。它直接激活并变构调节α1β2γ2 GABA A受体,尽管其作用位点尚不清楚。为深入了解卡立普多的作用,评估了该药物的亚基依赖性效应。从表达α1β2、α1β3或αxβzγ2(其中x = 1 - 6且z = 1 - 3)GABA A受体的HEK293细胞以及包含δ亚基的受体(模拟突触外受体)中获得全细胞膜片钳记录。在所有构型中均观察到直接开启和变构增强GABA门控电流的能力。γ2亚基的存在与否不影响卡立普多直接开启或变构调节受体的能力。β1亚基的存在相对于最大GABA电流赋予直接激活最高效力,而β2亚基的存在赋予GABA反应变构调节最高效力。关于α亚基,卡立普多在增强包含α1亚基的受体中GABA的作用方面最有效。无论α亚基异构体如何,直接开启受体的能力通常相当,尽管包含α3亚基的受体显示出直接开启效力和亲和力显著降低。在突触外(α1β3δ和α4β3δ)受体中,卡立普多作为直接开启激动剂比GABA具有更高的效力。此外,卡立普多在这些受体中变构增强了EC20和饱和GABA浓度。在评估电压依赖性时,我们发现直接开启和抑制作用对膜电压不敏感,而变构调节作用受膜电压影响。我们的研究结果表明卡立普多在突触和突触外GABA A受体上具有直接和变构效应,并且亚基异构体影响这些效应。