Ritta M N, Cardinali D P
Neurosci Lett. 1982 Aug 31;31(3):307-11. doi: 10.1016/0304-3940(82)90038-6.
Rat pineal glands incubated in vitro with 10 or 100 microM norepinephrine (NE) released 51% and 415% more prostaglandin E2 (PGE2) to the medium than in the absence of NE. Phentolamine (10 microM) prevented fully the effect of NE at both concentrations, whereas propranolol failed to affect it significantly. After superior cervical ganglionectomy (SCGx), NE-induced PGE2 release was significantly higher than in sham-operated controls--an effect also blocked by phentolamine but not by propranolol. These results suggest that NE releases PGE2 in rat pineals via alpha-adrenoceptors, acting at a post-synaptic site, and that SCGx induces alpha-adrenergic supersensitivity in the pinealocytes.
与在无去甲肾上腺素(NE)情况下相比,在体外培养的大鼠松果体与10或100微摩尔去甲肾上腺素(NE)一起孵育时,释放到培养基中的前列腺素E2(PGE2)分别多出51%和415%。酚妥拉明(10微摩尔)在两种浓度下都能完全阻止NE的作用,而普萘洛尔则未能对其产生显著影响。在颈上神经节切除术(SCGx)后,NE诱导的PGE2释放显著高于假手术对照组——酚妥拉明可阻断此效应,但普萘洛尔不能。这些结果表明,NE通过α-肾上腺素能受体在大鼠松果体中释放PGE2,作用于突触后位点,并且SCGx可诱导松果体细胞中的α-肾上腺素能超敏反应。