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儿茶酚胺对离体人结肠平滑肌的作用。

Effects of catecholamines on isolated human colonic smooth muscle.

作者信息

MacDonald A, McLaughlin D P, Fulton J, MacDonald E, Scott P J

机构信息

Department of Biological Sciences, Glasgow Caledonian University, UK.

出版信息

J Auton Pharmacol. 1996 Aug;16(4):213-20. doi: 10.1111/j.1474-8673.1996.tb00425.x.

Abstract
  1. The effects of catecholamines and some adrenoceptor agonists and antagonists on isolated preparations of human colonic smooth muscle obtained from surgical resections were examined. 2. Strips of circular smooth muscle displayed rhythmic myogenic spontaneous contractions which were inhibited by catecholamines with an order of potency of isoprenaline (1.0) > noradrenaline (0.32) > adrenaline (0.2). Phentolamine (0.7 microM) significantly shifted the noradrenaline concentration-response curve (CRC) to the right but had no significant effect on isoprenaline or adrenaline. Propranolol (1 microM) significantly shifted the isoprenaline to the right but had no significant effect on noradrenaline or adrenaline. 3. Salbutamol (30 microM) had no inhibitory effect on the spontaneous activity and ICI 118,551 (1 microM) had no effect on inhibitory responses to isoprenaline. Betaxolol (1 microM) significantly shifted the CRC to isoprenaline to the right. BRL 37344 had no effect on spontaneous activity. 4. Responsiveness of circular strips to catecholamines was not affected by age of the patient and no consistent differences between males and females were shown. 5. Strips of taenia coli exhibited little or no spontaneous phasic activity. Noradrenaline and isoprenaline relaxed KCl-induced tone. The effects of noradrenaline and isoprenaline were antagonized by propranolol but not by phentolamine. BRL 37344 had no effect on KCl-induced tone. 6. In conclusion, catecholamines relaxed spontaneous activity of human colon circular smooth muscle through an action on both alpha- and beta-adrenoceptors. The alpha-adrenoceptors were of the alpha 1-subtype. The beta-adrenoceptor-mediated relaxation appeared to be primarily beta 1. In taenia coli, catecholamines relaxed KCl-induced tone via beta-adrenoceptors only.
摘要
  1. 研究了儿茶酚胺以及一些肾上腺素能受体激动剂和拮抗剂对取自手术切除标本的人结肠平滑肌分离制剂的作用。2. 环形平滑肌条显示出有节律的肌源性自发收缩,儿茶酚胺可抑制这些收缩,其效力顺序为异丙肾上腺素(1.0)>去甲肾上腺素(0.32)>肾上腺素(0.2)。酚妥拉明(0.7微摩尔)使去甲肾上腺素浓度-反应曲线(CRC)显著右移,但对异丙肾上腺素或肾上腺素无显著影响。普萘洛尔(1微摩尔)使异丙肾上腺素的曲线显著右移,但对去甲肾上腺素或肾上腺素无显著影响。3. 沙丁胺醇(30微摩尔)对自发活动无抑制作用,ICI 118,551(1微摩尔)对异丙肾上腺素的抑制反应无影响。倍他洛尔(1微摩尔)使异丙肾上腺素的CRC显著右移。BRL 37344对自发活动无影响。4. 环形条对儿茶酚胺的反应性不受患者年龄影响,男性和女性之间未显示出一致差异。5. 结肠带条几乎没有或没有自发的阶段性活动。去甲肾上腺素和异丙肾上腺素可舒张氯化钾诱导的张力。普萘洛尔可拮抗去甲肾上腺素和异丙肾上腺素的作用,但酚妥拉明不能。BRL 37344对氯化钾诱导的张力无影响。6. 总之,儿茶酚胺通过作用于α和β肾上腺素能受体来舒张人结肠环形平滑肌的自发活动。α肾上腺素能受体为α1亚型。β肾上腺素能受体介导的舒张似乎主要是β1型。在结肠带中,儿茶酚胺仅通过β肾上腺素能受体舒张氯化钾诱导的张力。

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