Alkadhi K A, Al-Hijailan R S, Malik K, Hogan Y H
Department of Pharmacological and Pharmaceutical Sciences, College of Pharmacy, University of Houston, Houston, Texas 77204, USA.
J Neurosci. 2001 May 15;21(10):3515-20. doi: 10.1523/JNEUROSCI.21-10-03515.2001.
Carbon monoxide (CO), produced in the body by the enzyme heme oxygenase (HO), has been suggested as a retrograde synaptic messenger with a prominent role in the long-term potentiation (LTP) of certain areas of the brain. LTP of sympathetic ganglia is 5-HT(3) receptor-dependent and has been shown to require nitric oxide for the maintenance, but not for the induction, phase. We investigated the possibility of CO being required for the induction of ganglionic LTP. Pretreatment of rat isolated superior cervical ganglia with oxyhemoglobin (25-100 microm) completely blocked LTP. In the same ganglia, prolonged washout of oxyhemoglobin did not uncover any potentiation of the compound action potential. Oxyhemoglobin had no significant effect on the maintenance phase in ganglia with established LTP. Pretreatment of ganglia with the HO inhibitor zinc protoporphyrin-IX (ZnPP) (10 microm) completely and irreversibly prevented the expression of tetanus-evoked LTP. However, in the same ganglia, after superfusion of CO in the presence of ZnPP, tetanic stimulation readily evoked LTP. No effect was seen on the maintenance phase when ZnPP was superfused on ganglia with established LTP. Pretreatment of ganglia with the 5-HT(3) receptor antagonist ondansetron (0.4 microm) alone completely and irreversibly blocked LTP. However, in the presence of CO, ondansetron did not block LTP. These results suggest that activation of 5-HT(3) receptors may be involved in the production of CO. The results also suggest that CO, probably originating outside the presynaptic nerve terminal, is involved in the induction of LTP.
一氧化碳(CO)由血红素加氧酶(HO)在体内产生,有人提出它作为一种逆行性突触信使,在大脑某些区域的长时程增强(LTP)中起重要作用。交感神经节的LTP依赖于5-羟色胺(5-HT)3型受体,并且已表明其维持阶段需要一氧化氮,但诱导阶段不需要。我们研究了CO是否为神经节LTP诱导所必需。用氧合血红蛋白(25 - 100微摩尔)预处理大鼠离体颈上神经节可完全阻断LTP。在同一神经节中,长时间洗脱氧合血红蛋白并未发现复合动作电位有任何增强。氧合血红蛋白对已建立LTP的神经节的维持阶段无显著影响。用HO抑制剂原卟啉锌 - IX(ZnPP)(10微摩尔)预处理神经节可完全且不可逆地阻止破伤风诱发的LTP的表达。然而,在同一神经节中,在存在ZnPP的情况下灌注CO后,强直刺激很容易诱发LTP。当ZnPP灌注到已建立LTP的神经节上时,对维持阶段未见影响。单独用5-HT3型受体拮抗剂昂丹司琼(0.4微摩尔)预处理神经节可完全且不可逆地阻断LTP。然而,在有CO存在的情况下,昂丹司琼并不阻断LTP。这些结果表明5-HT3型受体的激活可能参与了CO的产生。结果还表明,可能起源于突触前神经末梢之外的CO参与了LTP的诱导。