Metsä-Ketelä T
Acta Physiol Scand. 1981 Aug;112(4):481-5. doi: 10.1111/j.1748-1716.1981.tb06847.x.
The effects of prostaglandin (PG) F2 alpha, E2, E1 and I2 on the amplitude, duration of the contraction-relaxation cycle (CRC), the second derivative of developed tension and the cyclic adenosine-3', 5' monophosphate (cAMP) level and on 45Ca uptake were studied in isolated spontaneously beating rat atria. The order of capacity to generate positive inotropic effects was PGF2 alpha greater than PGE2 greater than PGE1 approximately PGI2. Only PGI2 and PGE1 decreased the duration of CRC. PGF2 alpha produced an increase during the first 2.5 min, whereafter the duration returned to the initial level, PGE2 had no significant effect on the shape of the CRC. The ratios of the maximum and minimum of the second derivative of the developed tension were reduced by PGI2 and PGF2 alpha 2.5 and 5 min after administration, respectively. The 45Ca uptake was stimulated equally by all of the tested PGs, but only PGI2 and PGE1 could significantly increase the cAMP level. The results do not support the conception that cAMP could mediate the positive inotropic effect of PGs. Rather the contrary, cAMP, increased by PGE1 or PGI2, could be responsible for increased relaxation, which might prevent the full development of tension.
在离体自发搏动的大鼠心房中,研究了前列腺素(PG)F2α、E2、E1和I2对收缩-舒张周期(CRC)的幅度、持续时间、张力发展的二阶导数、环磷酸腺苷(cAMP)水平以及45Ca摄取的影响。产生正性肌力作用的能力顺序为PGF2α>PGE2>PGE1≈PGI2。只有PGI2和PGE1缩短了CRC的持续时间。PGF2α在最初2.5分钟内使CRC持续时间增加,之后又恢复到初始水平,PGE2对CRC的形状无显著影响。给药后2.5分钟和5分钟,PGI2和PGF2α分别降低了张力发展二阶导数的最大值与最小值之比。所有受试PG均同等程度地刺激45Ca摄取,但只有PGI2和PGE1能显著提高cAMP水平。这些结果不支持cAMP介导PG正性肌力作用的观点。相反,由PGE1或PGI2升高的cAMP可能导致舒张增强,这可能会阻碍张力的充分发展。