Parkman H P, Pagano A P, Vozzelli M A, Ryan J P
Department of Medicine, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
Am J Physiol. 1995 Sep;269(3 Pt 1):G418-26. doi: 10.1152/ajpgi.1995.269.3.G418.
The aims of this study were to determine regional differences and the mechanism of gastric contractile effects of erythromycin. Rabbit gastric circular muscle strips were studied in vitro. The threshold dose for erythromycin was significantly less and the maximum contraction greater in the antrum (1 microM and 0.9 +/- 0.3 kg/cm2) than in the fundus (10 microM and 0.3 +/- 0.1 kg/cm2). Erythromycin-induced antral contractions were decreased by motilin tachyphylaxis but unaffected by tetrodotoxin, atropine, hexamethonium, or ondansetron. At a subthreshold dose (0.1 microM), erythromycin increased the frequency, but not the amplitude, of bethanechol (10 +/- 3%)-and substance P-induced (13 +/- 5%) phasic antral contractions. This chronotropic effect was inhibited with tetrodotoxin, atropine, or motilin tachyphylaxis. Erythromycin (10 microM) and motilin (1 microM) enhanced the amplitude of substance P-induced tonic fundic contractions by 38 and 32%, respectively, without effect on bethanechol-induced contractions. In summary, erythromycin contracts antral muscle more potently and forcefully than fundic muscle. Erythromycin increases antral contractility by two mechanisms: an inotropic effect acting on smooth muscle motilin receptors, and, at lower doses, a cholinergic chronotropic effect mediated through neuronal motilin receptors.
本研究的目的是确定红霉素对胃收缩作用的区域差异及其机制。采用体外研究兔胃环形肌条。红霉素在胃窦部(1微摩尔和0.9±0.3千克/平方厘米)的阈剂量显著低于胃底部(10微摩尔和0.3±0.1千克/平方厘米),而最大收缩力则更大。胃动素快速耐受可降低红霉素诱导的胃窦收缩,但不受河豚毒素、阿托品、六甲铵或昂丹司琼的影响。在阈下剂量(0.1微摩尔)时,红霉素增加了氨甲酰甲胆碱(10±3%)和P物质诱导(13±5%)的胃窦相性收缩的频率,但不增加其幅度。这种变时效应可被河豚毒素、阿托品或胃动素快速耐受所抑制。红霉素(10微摩尔)和胃动素(1微摩尔)分别使P物质诱导的胃底部强直性收缩幅度增强38%和32%,而对氨甲酰甲胆碱诱导的收缩无影响。总之,红霉素对胃窦肌的收缩作用比胃底肌更有效、更强。红霉素通过两种机制增加胃窦收缩力:一种是作用于平滑肌胃动素受体的变力作用,另一种是在较低剂量时通过神经元胃动素受体介导的胆碱能变时作用。