Chaudhuri J, Donahue M J
Department of Biological Sciences, University of North Texas, Denton.
Mol Biochem Parasitol. 1989 Jul;35(3):191-8. doi: 10.1016/0166-6851(89)90205-3.
Serotonin (5-hydroxytryptamine, 5-HT) receptors in the muscle and intestinal tissues of adult Ascaris suum have been investigated. [3H] lysergic acid diethylamide (LSD) exhibited specific and saturable binding to membranes prepared from both intestine and muscle. The intestinal tissue membranes had an equilibrium dissociation constant (Kd) of 2.70 nM for LSD and a Kd of 2.50 microM for 5-HT. As compared to the intestine, the muscle membranes had comparatively higher affinity for both LSD (Kd = 1.80 nM) and 5-HT (Kd = 0.68 microM). The muscle membranes also had a high binding affinity for ketanserin, a 5-HT2 antagonist, (Kd = 16.7 nM) whereas intestinal membranes exhibited no specific binding of ketanserin. Serotonin significantly inhibited the binding of LSD to the intestinal and muscle tissue membranes while adrenergic and cholinergic drugs and histamine did not. This suggested that the binding of LSD, 5-HT and ketanserin to the parasite membranes was specific. Collectively, the data demonstrated the presence of a serotonin receptor in the muscle and intestinal tissues of the adult A. suum. The receptor in the muscle was pharmacologically similar to the mammalian serotonin type 2 receptor.
对成年猪蛔虫肌肉和肠道组织中的5-羟色胺(5-羟色氨酸,5-HT)受体进行了研究。[3H]麦角酸二乙酰胺(LSD)与从肠道和肌肉制备的膜呈现出特异性和饱和性结合。肠道组织膜对LSD的平衡解离常数(Kd)为2.70 nM,对5-HT的Kd为2.50 μM。与肠道相比,肌肉膜对LSD(Kd = 1.80 nM)和5-HT(Kd = 0.68 μM)的亲和力相对较高。肌肉膜对5-HT2拮抗剂酮色林也具有高结合亲和力(Kd = 16.7 nM),而肠道膜未表现出酮色林的特异性结合。5-羟色胺显著抑制LSD与肠道和肌肉组织膜的结合,而肾上腺素能、胆碱能药物和组胺则无此作用。这表明LSD、5-HT和酮色林与寄生虫膜的结合具有特异性。总体而言,数据证明成年猪蛔虫的肌肉和肠道组织中存在5-羟色胺受体。肌肉中的受体在药理学上与哺乳动物的5-羟色胺2型受体相似。