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普萘洛尔、噻吗洛尔和美托洛尔的(±)-、(+)-和(-)-异构体对大鼠离体右心室去甲肾上腺素能传递的影响。

Effects of the (+/-)-, (+)- and (-)-forms of propranolol, timolol and metoprolol on noradrenergic transmission in the rat isolated right ventricle.

作者信息

Bradley L, Doggrell S A

出版信息

Arch Int Pharmacodyn Ther. 1984 Jul;270(1):61-78.

PMID:6497503
Abstract

The effects of the (+/-)-, (+)- and (-)-forms of propranolol, timolol and metoprolol on noradrenergic transmission have been studied in the rat isolated right ventricle. (+)- And (-)-propranolol (10(-5) M) inhibited the accumulation of radioactivity from [3H]-noradrenaline. The decline in the spontaneous outflow of radioactivity, following loading of the tissue with [3H]-noradrenaline, was reduced by (+)- and (-)-propranolol (10(-5) M), (+)-timolol (10(-5) M), (-)-timolol (10(-6) - 10(-5) M) and (+)-metoprolol (10(-5) M). (+)-Propranolol, (+)-timolol (10(-6) M) and (+)- and (-)-metoprolol (10(-5) M) increased the decline in outflow of radioactivity evoked by field stimulation in the absence, but not in the presence, of lignocaine (10(-4) M), probably by decreasing nerve excitability. The ability of (-)-propranolol (10(-5) M) to increase the decline in evoked outflow was also reduced in the presence of lignocaine. (+)-Propranolol, (+)-timolol and (-)-metoprolol reduced the contractile response to field stimulation by a similar percentage in the absence or presence of lignocaine. The ability of (-)-propranolol and (+)-metoprolol (10(-5) M) to reduce contractile responses was decreased and abolished, respectively, by the addition of lignocaine. Evoked-outflow was not altered but contractile responses were inhibited by (-)-timolol (10(-7) - 10(-5) M) and (-)-metoprolol (10(-5) M). Contractile responses to isoprenaline were not altered by (+)-propranolol, (+)-timolol (10(-7) M) and (+)-metoprolol (10(-7) - 10(-6) M). (+)- Or (-)-propranolol (10(-7) M) and (+)-timolol (10(-6) M) had no effect on the rate of beating to isoprenaline but reduced the force whereas (+/-)-metoprolol (10(-7) M) had no effect on the force but reduced the rate of beating. The rate of beating and force responses to isoprenaline were reduced by (+/-)-, (+)-, (-)-propranolol (10(-6) M), (+/-)- or (-)-timolol (10(-7) - 10(-6) M), (+/-)-metoprolol (10(-6) M) and (-)-metoprolol (10(-7) - 10(-6) M). The data suggest that, in the rat isolated right ventricle, the (+)-isomers are active constituents of (+/-)-propranolol and (+/-)-timolol but not of (+/-)-metoprolol.

摘要

在大鼠离体右心室中研究了普萘洛尔、噻吗洛尔和美托洛尔的(±)-、(+)-和(-)-异构体对去甲肾上腺素能传递的影响。(+)-和(-)-普萘洛尔(10⁻⁵M)抑制了[³H]-去甲肾上腺素的放射性积累。在用[³H]-去甲肾上腺素加载组织后,放射性自发流出的下降被(+)-和(-)-普萘洛尔(10⁻⁵M)、(+)-噻吗洛尔(10⁻⁵M)、(-)-噻吗洛尔(10⁻⁶ - 10⁻⁵M)和(+)-美托洛尔(10⁻⁵M)所降低。在不存在(但在存在时不)利多卡因(10⁻⁴M)的情况下,(+)-普萘洛尔、(+)-噻吗洛尔(10⁻⁶M)以及(+)-和(-)-美托洛尔(10⁻⁵M)增加了场刺激诱发的放射性流出下降,这可能是通过降低神经兴奋性实现的。在存在利多卡因的情况下,(-)-普萘洛尔(10⁻⁵M)增加诱发流出下降的能力也降低了。在不存在或存在利多卡因的情况下,(+)-普萘洛尔、(+)-噻吗洛尔和(-)-美托洛尔以相似的百分比降低了对场刺激的收缩反应。加入利多卡因后,(-)-普萘洛尔和(+)-美托洛尔(10⁻⁵M)降低收缩反应的能力分别降低和消除。(-)-噻吗洛尔(10⁻⁷ - 10⁻⁵M)和(-)-美托洛尔(10⁻⁵M)不改变诱发流出但抑制收缩反应。(+)-普萘洛尔、(+)-噻吗洛尔(10⁻⁷M)和(+)-美托洛尔(10⁻⁷ - 10⁻⁶M)不改变对异丙肾上腺素的收缩反应。(+)-或(-)-普萘洛尔(10⁻⁷M)和(+)-噻吗洛尔(10⁻⁶M)对异丙肾上腺素引起的心跳速率没有影响,但降低了力量,而(±)-美托洛尔(10⁻⁷M)对力量没有影响,但降低了心跳速率。(±)-、(+)-、(-)-普萘洛尔(10⁻⁶M)、(±)-或(-)-噻吗洛尔(10⁻⁷ - 10⁻⁶M)、(±)-美托洛尔(10⁻⁶M)和(-)-美托洛尔(10⁻⁷ - 10⁻⁶M)降低了对异丙肾上腺素的心跳速率和力量反应。数据表明,在大鼠离体右心室中,(+)-异构体是(±)-普萘洛尔和(±)-噻吗洛尔的活性成分,但不是(±)-美托洛尔的活性成分。

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