Szallasi A, Blumberg P M
Molecular Mechanisms of Tumor Promotion Section, National Cancer Institute, Bethesda, MD 20892.
Naunyn Schmiedebergs Arch Pharmacol. 1993 Jan;347(1):84-91. doi: 10.1007/BF00168777.
Specific binding of [3H]resiniferatoxin (RTX) is thought to represent the vanilloid (capsaicin) receptor. In the present study, we have used this binding assay to elucidate the contribution of differential receptor expression to the capsaicin-resistance of hamsters and rabbits; binding parameters were compared to those of species (rats, mice) regarded as capsaicin-sensitive. Whereas the 5-fold lower affinity for [3H]RTX binding in the hamster (100 pM) as compared to the rat (20 pM) is unlikely to account for the 100-fold difference in the in vivo responses of RTX-induced inflammation and hypothermia, the lack of detectable specific [3H]RTX binding sites in the rabbit might represent the predominant mechanism of capsaicin-resistance in this species. Regulation of the vanilloid receptor was further characterized in the rat. In accord with the temperature dependence of both in vivo and in vitro capsaicin actions, we found a marked temperature dependence for association rates. Dissociation turned out to have complex kinetics dependent on time and receptor occupancy. Low pH (5.5-7.0) did not affect receptor binding. Preincubation with heavy metal cations and other sulfhydryl-reactive agents inhibited specific [3H]RTX binding indicating that the vanilloid receptor is a thiol-protein, and that free sulfhydryl groups play an essential role in agonist binding activity. Preliminary characterization suggested noncompetitive inhibition.
[3H]树脂毒素(RTX)的特异性结合被认为代表香草酸(辣椒素)受体。在本研究中,我们利用这种结合测定法来阐明受体表达差异对仓鼠和兔子辣椒素抗性的影响;将结合参数与被认为对辣椒素敏感的物种(大鼠、小鼠)的参数进行比较。与大鼠(20 pM)相比,仓鼠对[3H]RTX结合的亲和力低5倍(100 pM),这不太可能解释RTX诱导的炎症和体温过低的体内反应中100倍的差异,而兔子中缺乏可检测到的特异性[3H]RTX结合位点可能代表该物种辣椒素抗性的主要机制。在大鼠中进一步研究了香草酸受体的调节。与体内和体外辣椒素作用的温度依赖性一致,我们发现结合速率有明显的温度依赖性。解离结果显示具有复杂的动力学,依赖于时间和受体占有率。低pH(5.5 - 7.0)不影响受体结合。用重金属阳离子和其他巯基反应剂预孵育会抑制特异性[3H]RTX结合,表明香草酸受体是一种硫醇蛋白,并且游离巯基在激动剂结合活性中起重要作用。初步特征表明存在非竞争性抑制。