Itoh Z, Suzuki T, Nakaya M, Inoue M, Mitsuhashi S
Antimicrob Agents Chemother. 1984 Dec;26(6):863-9. doi: 10.1128/AAC.26.6.863.
For clarification of the nature of the side effects of macrolide antibiotics on the gastrointestinal tract, the motor-stimulating activity of these agents was studied in unanesthetized dogs. The results showed that erythromycin and oleandomycin, the 14-membered macrolides with two side chain sugars combined at C3 and C5 in a glycosidic linkage in parallel, strongly stimulate gastrointestinal motor activity, an action accompanied by vomiting at large doses. On the other hand, leucomycin, acetylspiramycin, and tylosin, belonging to a 16-membered macrolide with two side chain sugars in series combined at C5 of the lactone ring, did not induce contractions of the gastrointestinal tract. Motor-stimulating activity by erythromycin and oleandomycin was greatly inhibited by atropine sulfate. These results point to structure-physiological activity relationships.
为阐明大环内酯类抗生素对胃肠道副作用的本质,在未麻醉的犬中研究了这些药物的促运动活性。结果表明,红霉素和竹桃霉素,这两种具有两个侧链糖以糖苷键平行结合在C3和C5位置的14元大环内酯类药物,强烈刺激胃肠道运动活性,大剂量时会伴有呕吐。另一方面,吉他霉素、乙酰螺旋霉素和泰乐菌素属于具有两个侧链糖在内酯环C5位置串联结合的16元大环内酯类药物,不会引起胃肠道收缩。硫酸阿托品可极大地抑制红霉素和竹桃霉素的促运动活性。这些结果表明了结构与生理活性之间的关系。