Yoo K Y, Lee J, Kim H S, Jeong S W
Department of Anesthesiology, Chonnam National University Medical School, Kwangju, South Korea.
Anesth Analg. 2001 Apr;92(4):1006-9. doi: 10.1097/00000539-200104000-00037.
We determined the effects of fentanyl, sufentanil, morphine, and meperidine on the spontaneous contractility of isolated human pregnant uterine muscle strips. Uterine specimens were obtained from normal full-term parturients undergoing elective lower-segment cesarean delivery. Longitudinal muscle strips were prepared and mounted vertically in tissue chambers to record their isometric tension. Opioid concentration-response curves were constructed after rhythmic contractions were established. The responses were also examined in the presence of opioid receptor blocker, nitric oxide synthase inhibitor, beta-adrenoceptor blocker, or cyclooxygenase inhibitor. Fentanyl and meperidine inhibited uterine contractility in a concentration-dependent manner, their concentration that inhibited 50% being 2.3 x 10(-6) and 1.0 x 10(-3)M, respectively. Sufentanil and morphine had no significant effects on uterine contractility. Pretreatment with either naloxone, N(G)-nitro-L-arginine methyl ester, atenolol, or indomethacin did not affect the uterine responses to opioids. These results demonstrate that fentanyl and meperidine may have direct inhibitory effects on the contractility of the human uterus, though at supraclinical concentrations.
Opioids do not have a significant effect on spontaneous contractions of gravid human uterine muscle at their clinically relevant concentrations.
我们确定了芬太尼、舒芬太尼、吗啡和哌替啶对离体人妊娠子宫肌条自发收缩性的影响。子宫标本取自接受择期下段剖宫产的足月正常产妇。制备纵向肌条并垂直安装在组织浴槽中以记录其等长张力。在建立节律性收缩后绘制阿片类药物浓度-反应曲线。还在存在阿片受体阻滞剂、一氧化氮合酶抑制剂、β-肾上腺素能受体阻滞剂或环氧化酶抑制剂的情况下检查反应。芬太尼和哌替啶以浓度依赖性方式抑制子宫收缩,其抑制50%的浓度分别为2.3×10⁻⁶和1.0×10⁻³M。舒芬太尼和吗啡对子宫收缩无显著影响。用纳洛酮、N(G)-硝基-L-精氨酸甲酯、阿替洛尔或吲哚美辛预处理不影响子宫对阿片类药物的反应。这些结果表明,芬太尼和哌替啶可能对人子宫收缩有直接抑制作用,尽管是在超临床浓度下。
阿片类药物在其临床相关浓度下对妊娠人子宫肌的自发收缩无显著影响。