Camilleri M
Enteric Neuroscience Program, Gastroenterology Research Unit, Mayo Clinic and Mayo Foundation, Rochester, MN 55905, USA.
Aliment Pharmacol Ther. 2001 Mar;15(3):277-89. doi: 10.1046/j.1365-2036.2001.00925.x.
Tegaserod (Zelmac), an aminoguanidine indole derivative of serotonin, is a selective partial agonist highly selective for 5-HT(4) receptor with an affinity constant in the nanomolar range. Tegaserod does not cause adverse pharmacodynamic effects, is absorbed rapidly after oral administration and distributes widely into tissues. Pharmacokinetics of oral tegaserod are linear in the 2--12 mg dose range. After oral administration tegaserod is metabolized mainly pre-systemically; when absorbed, intact tegaserod is excreted as N-glucuronides mainly via the bile. No clinically relevant drug--drug interactions were identified. Tegaserod has proven safe in toxicity studies. In pharmacodynamic studies, tegaserod stimulated the peristaltic reflex in vitro, increased canine intestinal and colonic motility and transit, reduced visceral afferent firing or sensation in response to distension in animals, and accelerated gastric, small bowel and colonic transit in healthy patients, and small bowel transit in patients with constipation-predominant irritable bowel syndrome. Three large phase III randomized, double-blinded, and placebo-controlled trials were performed predominantly in females (approximately 85%) with constipation-predominant irritable bowel syndrome. Overall, phase III results support efficacy as assessed by the subject's global assessment of relief with significant improvement in secondary endpoints such as abdominal pain, bowel frequency and consistency. Tegaserod was well-tolerated; the most frequent adverse event was transient diarrhoea.
替加色罗(泽马可)是一种血清素的氨基胍吲哚衍生物,是一种对5-HT(4)受体具有高度选择性的选择性部分激动剂,其亲和常数在纳摩尔范围内。替加色罗不会引起不良药效学效应,口服给药后吸收迅速,并广泛分布于组织中。口服替加色罗在2-12mg剂量范围内药代动力学呈线性。口服给药后,替加色罗主要在体循环前被代谢;吸收后,完整的替加色罗以N-葡萄糖醛酸苷的形式主要通过胆汁排泄。未发现临床相关的药物相互作用。替加色罗在毒性研究中已被证明是安全的。在药效学研究中,替加色罗在体外刺激蠕动反射,增加犬肠道和结肠的运动性及传输,减少动物对扩张的内脏传入放电或感觉,并加速健康患者胃、小肠和结肠的传输,以及便秘型肠易激综合征患者的小肠传输。三项大型III期随机、双盲、安慰剂对照试验主要在女性(约85%)便秘型肠易激综合征患者中进行。总体而言,III期结果支持受试者总体缓解评估所评估的疗效,次要终点如腹痛、排便频率和大便性状有显著改善。替加色罗耐受性良好;最常见的不良事件是短暂性腹泻。