Arata A, Onimaru H, Homma I
Department of Physiology, Showa University, School of Medicine, Tokyo, Japan.
Brain Res. 1993 Mar 12;605(2):193-9. doi: 10.1016/0006-8993(93)91740-j.
Involvement of cAMP in the generation of respiratory rhythm was studied in newborn rat brainstem-spinal cord preparations. The respiratory rhythm was monitored by C4 inspiratory activity and/or pre-inspiratory (Pre-I) activity of neurons in the rostral ventrolateral medulla; previously suggested to be primary rhythm generating neurons which have pacemaker properties. The effects of four cAMP-increasing agents (forskolin, IBMX, Db-cAMP, and 8-Br-cAMP) on this neuronal activity were examined. Perfusion with forskolin (3-10 microM) increased the burst rate of C4 inspiratory activity in 20 of 32 preparations, but in 8 of those the increase was preceded by transient depression. The facilitation of the respiratory rhythm was greater whenever the burst rate before forskolin treatment was lower. The Pre-I neuron burst rate, which was recorded together with C4 activity, predominantly increased with forskolin treatment. The effects of IBMX, Db-cAMP and 8-Br-cAMP were similar to those of forskolin, but they were slightly less potent. Long-lasting depression of the respiratory rhythm (C4 and Pre-I activity) by clonidine, which might decrease intracellular cAMP level via alpha 2-receptors, was reversed by forskolin. To investigate the direct effects of the cAMP-increasing agents on Pre-I neurons, Pre-I activity was isolated by blocking the chemical synaptic transmission by incubation in a low Ca solution (0.2 mM Ca2+, 5 mM Mg2+). Forskolin (5-10 microM), IBMX (5-10 microM), Db-cAMP (0.2-0.4 mM), and 8-Br-cAMP (0.4-0.75 mM) all enhanced the burst rate of isolated Pre-I neurons.(ABSTRACT TRUNCATED AT 250 WORDS)
在新生大鼠脑干-脊髓标本中研究了环磷酸腺苷(cAMP)参与呼吸节律产生的情况。通过延髓头端腹外侧神经元的C4吸气活动和/或吸气前(Pre-I)活动来监测呼吸节律;此前认为这些神经元是具有起搏特性的主要节律产生神经元。研究了四种增加cAMP的药物(福斯可林、异丁基甲基黄嘌呤、二丁酰环磷腺苷钙和8-溴环磷腺苷)对这种神经元活动的影响。用福斯可林(3-10微摩尔)灌注时,32个标本中有20个的C4吸气活动爆发频率增加,但其中8个在增加之前有短暂的抑制。福斯可林治疗前爆发频率越低,呼吸节律的促进作用越大。与C4活动同时记录的Pre-I神经元爆发频率在福斯可林治疗后主要增加。异丁基甲基黄嘌呤、二丁酰环磷腺苷钙和8-溴环磷腺苷的作用与福斯可林相似,但效力稍弱。可乐定可能通过α2受体降低细胞内cAMP水平,从而导致呼吸节律(C4和Pre-I活动)的持久抑制,而福斯可林可逆转这种抑制。为了研究增加cAMP的药物对Pre-I神经元的直接作用,通过在低钙溶液(0.2毫摩尔钙离子、5毫摩尔镁离子)中孵育来阻断化学突触传递,从而分离出Pre-I活动。福斯可林(5-10微摩尔)、异丁基甲基黄嘌呤(5-10微摩尔)、二丁酰环磷腺苷钙(0.2-0.4毫摩尔)和8-溴环磷腺苷(0.4-0.75毫摩尔)均提高了分离出的Pre-I神经元的爆发频率。(摘要截选至250词)