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肾上腺素对去大脑家兔去甲肾上腺素释放的双重作用。

Dual effect of adrenaline on noradrenaline release in the pithed rabbit.

作者信息

Majewski H, Hedler L, Schurr C, Starke K

出版信息

J Cardiovasc Pharmacol. 1985 Mar-Apr;7(2):251-7. doi: 10.1097/00005344-198503000-00007.

Abstract

We examined the effects of adrenaline on the noradrenaline release rate and plasma catecholamine levels in the pithed rabbit with electrically stimulated sympathetic outflow (3 Hz). Adrenaline (0.06 micrograms/kg/min) increased the rate of noradrenaline release into the plasma. This increase was prevented by propranolol (0.2 mg/kg + 0.1 mg/kg/h) and probably involves activation of presynaptic beta-adrenoceptors. A higher dose of adrenaline (1.0 micrograms/kg/min) significantly reduced the noradrenaline release rate. The reduction was "reversed" to a facilitatory effect by phenoxybenzamine (4 mg/kg). Propranolol alone slightly inhibited the noradrenaline release rate. After pretreatment with desipramine (1.0 mg/kg + 0.2 mg/kg/h), the inhibitory effect of propranolol on noradrenaline release was more pronounced and blood pressure was also lowered. However, in rabbits pretreated with captopril (1 mg/kg) in addition to desipramine, the sympathoinhibitory effect of propranolol was not observed. These results suggest that adrenaline can activate either presynaptic beta-adrenoceptors to increase noradrenaline release or, in higher doses, presynaptic alpha-adrenoceptors to inhibit noradrenaline release in vivo. The decrease in the noradrenaline release rate produced by propranolol alone may not be due to blockade of facilitatory presynaptic beta-adrenoceptors, but rather to depression of renin secretion. This would decrease angiotensin II formation and hence decrease the presynaptic release-enhancing effect of angiotensin II.

摘要

我们研究了肾上腺素对去大脑家兔经电刺激交感神经传出纤维(3赫兹)时去甲肾上腺素释放速率和血浆儿茶酚胺水平的影响。肾上腺素(0.06微克/千克/分钟)可增加血浆中去甲肾上腺素的释放速率。普萘洛尔(0.2毫克/千克 + 0.1毫克/千克/小时)可阻止这种增加,这可能涉及突触前β-肾上腺素能受体的激活。更高剂量的肾上腺素(1.0微克/千克/分钟)可显著降低去甲肾上腺素的释放速率。苯苄胺(4毫克/千克)可将这种降低“逆转”为促进作用。单独使用普萘洛尔可轻微抑制去甲肾上腺素的释放速率。用去甲丙咪嗪(1.0毫克/千克 + 0.2毫克/千克/小时)预处理后,普萘洛尔对去甲肾上腺素释放的抑制作用更明显,血压也降低。然而,在除了去甲丙咪嗪还预先用卡托普利(1毫克/千克)处理的家兔中,未观察到普萘洛尔的交感神经抑制作用。这些结果表明,肾上腺素在体内可激活突触前β-肾上腺素能受体以增加去甲肾上腺素释放,或在更高剂量时激活突触前α-肾上腺素能受体以抑制去甲肾上腺素释放。单独使用普萘洛尔导致的去甲肾上腺素释放速率降低可能不是由于阻断了促进性突触前β-肾上腺素能受体,而是由于肾素分泌受抑制。这会减少血管紧张素II的形成,从而降低血管紧张素II的突触前释放增强作用。

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