Schümann H J, Endoh S, Brodde O E
Naunyn Schmiedebergs Arch Pharmacol. 1975;289(3):291-302. doi: 10.1007/BF00499982.
In the isolated papillary muscle of the rabbit the time course of the effects of selective beta- and alpha-adrenoceptor stimulation by isoprenaline and methoxamine, respectively, on the contractile force and on the level of 3',5'-cyclic AMP (cAMP) was determined. 1. Isoprenaline (3 times 10(-7) M) increased significantly the content of cAMP at 15 sec and elevated it to the maximal level-about twice the control value-at 30 sec after its administration, while the developed tension of the papillary muscle was also increased significantly at 15 sec and reached gradually its maximum at 90 sec. 2. Compared with isoprenaline methoxamine (10(-4) M) increased the developed tension very slowly: the maximal response was reached after 20 min. The level of cAMP, on the other hand, was changed neither before nor during the induction of the positive inotropic effect of methoxamine. 3. The phosphodiesterase inhibitor papaverine (10(-5) M) inhibited the PDE activity of the papillary muscle by about 40% after an incubation of 1 hr, and increased the level of cAMP significantly. The effects of isoprenaline on the contractile forced and on the level of cAMP were considerably enhanced by papaverine: the content of cAMP was increased by isoprenaline (3 times 10(-7) M) to about 3 times the control value and also its positive inotropic effect was significantly greater than in controls without papaverine. On the other hand, the positive inotropic effect of methoxamine (10(-4) M) was not affected by papaverine (10(-5) M). Furthermore, in the papillary muscle treated with papaverine the level of cAMP was significantly reduced by methoxamine: the papaverine-induced increase of cAMP was abolished by methoxamine. 4. The present results are compatible with the hypothesis that cAMP is involved as a mediator in the positive inotropic effect induced by beta-adrenoceptor stimulation, and indicate further that the stimulation of alpha-adrenoceptors evokes its positive inotropic effec through a mechanism other than that elicited by beta-adrenoceptor stimulation, i.e., independent of cAMP.
在兔离体乳头肌中,分别测定了异丙肾上腺素和甲氧明对β - 肾上腺素能受体和α - 肾上腺素能受体的选择性刺激对收缩力及3',5'-环磷酸腺苷(cAMP)水平的影响时程。1. 异丙肾上腺素(3×10⁻⁷ M)给药后15秒显著增加cAMP含量,30秒时升高至最大值——约为对照值的两倍,而乳头肌的张力在15秒时也显著增加,并在90秒时逐渐达到最大值。2. 与异丙肾上腺素相比,甲氧明(10⁻⁴ M)使张力增加非常缓慢:20分钟后达到最大反应。另一方面,在甲氧明产生正性肌力作用之前及过程中,cAMP水平均未改变。3. 磷酸二酯酶抑制剂罂粟碱(10⁻⁵ M)孵育1小时后,抑制乳头肌的磷酸二酯酶活性约40%,并显著增加cAMP水平。罂粟碱使异丙肾上腺素对收缩力和cAMP水平的作用显著增强:异丙肾上腺素(3×10⁻⁷ M)使cAMP含量增加至对照值约3倍,其正性肌力作用也显著大于未用罂粟碱的对照组。另一方面,甲氧明(10⁻⁴ M)的正性肌力作用不受罂粟碱(10⁻⁵ M)影响。此外,在经罂粟碱处理的乳头肌中,甲氧明使cAMP水平显著降低:甲氧明消除了罂粟碱诱导的cAMP增加。4. 目前的结果与cAMP作为β - 肾上腺素能受体刺激诱导的正性肌力作用的介质这一假说相符,并进一步表明α - 肾上腺素能受体的刺激通过不同于β - 肾上腺素能受体刺激所引发的机制,即独立于cAMP的机制,产生其正性肌力作用。