Porter D G, Downing S J, Bradshaw J M
J Endocrinol. 1979 Nov;83(2):183-92. doi: 10.1677/joe.0.0830183.
Porcine relaxin (250 guinea-pig units/mg) infused intravenously into anaesthetized rats at 20 micrograms/h reversibly abolished spontaneous intra-uterine pressure cycles yet left the myometrium responsive to oxytocin in doses of 4--8 mu. The inhibition was found to be primarily of the frequency, rather than of the amplitude, of pressure cycles. Relaxin (5 or 10 micrograms) was capable of completely suppressing uterine activity driven by prostaglandin F2 alpha infusion in oestrogen-treated ovariectomized rats. Whereas the beta-adrenergic blocker, propranolol, had no effect on relaxin-induced inhibition, phentolamine, an alpha-blocker, significantly delayed the relaxin effect. It is unlikely, however, that relaxin operates through an alpha-inhibitory receptor. The results show that relaxin acts primarily as a frequency modulator and is capable of antagonizing an exogenous myometrial stimulant.
将猪松弛素(250豚鼠单位/毫克)以20微克/小时的速度静脉注射到麻醉的大鼠体内,可使子宫内自发压力周期可逆性消失,但子宫肌层对4 - 8微单位剂量的催产素仍有反应。发现这种抑制主要作用于压力周期的频率,而非幅度。松弛素(5或10微克)能够完全抑制雌激素处理的去卵巢大鼠中前列腺素F2α输注所驱动的子宫活动。虽然β-肾上腺素能阻滞剂普萘洛尔对松弛素诱导的抑制作用没有影响,但α-阻滞剂酚妥拉明显著延迟了松弛素的作用。然而,松弛素不太可能通过α抑制性受体发挥作用。结果表明,松弛素主要作为频率调节剂起作用,并且能够拮抗外源性子宫肌层刺激物。