Stjernquist M, Owman C
Acta Physiol Scand. 1985 Jul;124(3):429-36. doi: 10.1111/j.1748-1716.1985.tb07679.x.
The isolated circular smooth muscle of the uterine cervix from spayed rats was investigated in vitro. One group of animals was treated with oestrogen. Preparations from these rats showed no spontaneous contractile activity, but responded with contractions to electrical field stimulation. The contractions were blocked by approximately 85% with atropine, scopolamine and tetrodotoxin, but were unaffected by the adrenergic antagonists propranolol, phenoxybenzamine, and yohimbine. This neurogenic effect was potentiated by neostigmine. Noradrenaline inhibited the nerve-induced contractions and also lowered resting tension in a concentration-dependent way. The latter effect of noradrenaline was inhibited by propranolol. The indirect effects of noradrenaline on the electrically induced contractions were also inhibited by propranolol, but potentiated with phenoxybenzamine and, to a less extent, yohimbine. Nerve-induced relaxation was never observed. Acetylcholine contracted the smooth muscle by an effect that was counteracted by atropine. A second group of spayed rats was not given any steroid treatment. The cervix preparations from these animals showed spontaneous activity, which was uninfluenced by atropine, propranolol, phenoxybenzamine, yohimbine, and tetrodotoxin. Noradrenaline inhibited the spontaneous activity. This noradrenergic effect was counteracted by propranolol and potentiated by phenobenzamine. Acetylcholine increased the smooth-muscle tone by an atropine-sensitive action. The results suggest the presence of a cholinergic motor innervation on the non-pregnant rat uterine cervix. The cervix also receives an adrenergic innervation, which may act both post-junctionally (lowering resting tension and inhibiting spontaneous activity) and prejunctionally (modulating the cholinergic nerves) via beta-adrenergic as well as alpha-adrenergic receptors.
对切除卵巢的大鼠子宫颈分离出的环形平滑肌进行了体外研究。一组动物用雌激素处理。这些大鼠的标本未表现出自发性收缩活动,但对电场刺激有收缩反应。阿托品、东莨菪碱和河豚毒素可使收缩反应阻断约85%,但不受肾上腺素能拮抗剂普萘洛尔、酚苄明和育亨宾的影响。新斯的明可增强这种神经源性效应。去甲肾上腺素抑制神经诱导的收缩,并以浓度依赖的方式降低静息张力。普萘洛尔可抑制去甲肾上腺素的后一种效应。普萘洛尔也可抑制去甲肾上腺素对电诱导收缩的间接效应,但酚苄明可增强这种效应,育亨宾在较小程度上也有增强作用。从未观察到神经诱导的舒张。乙酰胆碱通过一种被阿托品抵消的作用使平滑肌收缩。第二组切除卵巢的大鼠未接受任何类固醇治疗。这些动物的子宫颈标本表现出自发性活动,不受阿托品、普萘洛尔、酚苄明、育亨宾和河豚毒素的影响。去甲肾上腺素抑制自发性活动。这种去甲肾上腺素能效应被普萘洛尔抵消,被酚苄明增强。乙酰胆碱通过一种对阿托品敏感的作用增加平滑肌张力。结果表明,未孕大鼠子宫颈存在胆碱能运动神经支配。子宫颈也接受肾上腺素能神经支配,它可通过β-肾上腺素能受体以及α-肾上腺素能受体在接头后起作用(降低静息张力并抑制自发性活动),在接头前起作用(调节胆碱能神经)。