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首页> 外文期刊>Japanese Journal of Pharmacology >INFLUENCE OF HYPOTHYROID STATUS ON DOPAMINEIN-DUCED POSITIVE CHRONOTROPIC AND INOTROPIC EFFECTS ON ISOLATED RAT ATRIA
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INFLUENCE OF HYPOTHYROID STATUS ON DOPAMINEIN-DUCED POSITIVE CHRONOTROPIC AND INOTROPIC EFFECTS ON ISOLATED RAT ATRIA

机译:甲状腺液状态对多巴胺诱导的大鼠孤立性心房的正性和负性影响

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References(18) Cited-By(1) The involvement of α- and β-adrenoceptors in dopamine (DA)-induced positive chronotropic and inotropic effects was investigated in isolated atria from euthyroid and hypothyroid rats. Propranolol at 3×10-7 M remarkably inhibited the positive chronotropic effect of DA in both euthyroid and hypothyroid rats, and 1×10-6 M phentolamine inhibited the effects of DA in the presence of propranolol in hypothyroid rats. Propranolol remarkably inhibited the positive inotropic effect of DA in both euthyroid and hypothyroid rats, while phentolamine was effective only in hypothyroid rats. In atria from reserpinized rats, the pD2-values for DA in both chronotropic and inotropic effects were reduced, but effectiveness of propranolol or phentolamine on DA-induced positive chronotropic and inotropic effects in euthyroid and hypothyroid rats was similar to that in non-reserpinized rats. In hypothyroid rats, DA increased the maximal rate of tension development, which was inhibited by both phentolamine and propranolol. DA shortened the duration of contraction. DA in the presence of phentolamine significantly shortened the duration of contraction but did not in the presence of propranolol. In conclusion the DA-induced positive chronotropic effect is mainly produced by β-adrenoceptor stimulation in both euthyroid and hypothyroid rats, and also by α-adrenoceptors to some extent in hypothyroid rats. The DA-induced positive inotropic effect is produced by α- as well as β-adrenoceptor stimulation in both groups. However, α-adrenoceptors were involved to a greater extent in hypothyroid rats than in euthyroid rats. The stimulation of α-adrenoceptors by DA causes an increase in the maximal rate of tension development without a significant change in the duration of contraction, and the stimulation of β-adrenoceptors by DA causes an increase in the maximal rate of tension development and shortening of the duration of contraction.
机译:参考文献(18)被引用的By(1)在来自甲状腺和甲状腺功能低下大鼠的独立心房中研究了α-和β-肾上腺素能受体参与多巴胺(DA)引起的正变时性和变力作用。普萘洛尔在3×10-7 M时能明显抑制正常甲状腺和甲状腺功能减退的大鼠DA的变时性作用,而1×10-6 M酚妥拉明在存在甲状腺功能低下的大鼠中存在普萘洛尔时会抑制DA的正性变力作用。普萘洛尔在正常甲状腺和甲状腺功能减退的大鼠中均显着抑制DA的正性肌力作用,而酚妥拉明仅在甲状腺功能减退的大鼠中有效。在再固定化大鼠的心房中,变时性和变力作用中DA的pD2值均降低,但是普萘洛尔或酚妥拉明对正常人和甲状腺功能减退的大鼠DA引起的变时性和变力作用的正效应与未定形的大鼠相似。在甲状腺功能减退的大鼠中,DA增加了最大的紧张发展速度,苯妥拉明和普萘洛尔均能抑制这种发展。 DA缩短了收缩时间。酚妥拉明存在时,DA可以显着缩短收缩时间,但普萘洛尔不存在。总之,DA诱导的正变时性作用主要是由正常甲状腺和甲状腺功能减退的大鼠中的β-肾上腺素能受体刺激产生的,在某种程度上也由甲状腺功能减退的大鼠中的α-肾上腺素能受体产生。两组都通过α-和β-肾上腺素受体刺激产生DA诱导的正性肌力作用。然而,甲状腺功能低下的大鼠中α-肾上腺素能受体的参与程度高于正常甲状腺的大鼠。 DA刺激α-肾上腺素能引起最大的张力发展速率增加,而收缩持续时间没有明显变化,DA刺激β-肾上腺素能受体引起的最大张力产生速率增加,而收缩时间缩短。收缩的持续时间。

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