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Effects of Phenylephrine on Spontaneous Activity and L-Type Ca 2+ Current in Isolated Corpus Cavernosum Myocytes

机译:苯肾上腺素对离体海绵体心肌细胞自发活性和L型Ca 2+电流的影响

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Introduction. Norepinephrine is important in maintaining detumescent tone in the corpus cavernosum, although the mechanism is incompletely understood. As α-adrenoceptor-induced tone is antagonized by L-type Ca 2+ channel blockers, it is usually assumed that direct modulation of this current is involved. However, the effects of α-adrenoceptor agonists have never been directly examined on L-type current in corpus cavernosum myocytes (CCSMC), leaving open other possibilities. In particular, CCSMC are now known to develop spontaneous tone via a pacemaker mechanism involving spontaneous Ca 2+ waves that activate Cl - currents, causing depolarization and voltage-dependent activation of L-type channels. We hypothesized that phenylephrine modulates tone via this system, rather than by directly activating L-type channels. Aims. Examine in freshly isolated CCSMC the effect of phenylephrine on: (i) spontaneous Cl - currents and depolarizations; (ii) cytosolic Ca 2+ waves; and (iii) L-type current. Methods. CCSMC were enzymatically dispersed from male New Zealand White rabbits for patch clamp recording and real time Ca 2+ imaging. Main Outcome Measures. Spontaneous Cl - currents, spontaneous depolarizations, cytosolic Ca 2+ and L-type current. Results. Phenylephrine enhanced the amplitude and frequency of spontaneous Cl - currents, increased the duration and frequency of spontaneous depolarizations and increased the frequency of spontaneous Ca 2+ waves. These effects were blocked by 2-aminoethoxy diphenylborate (2-APB), suggesting that they were mediated by IP 3-induced Ca 2+ release from intracellular stores. In contrast, 2-APB had no effect on Ca 2+ transients evoked by releasing stored Ca 2+ with caffeine, suggesting that it had little effect on store Ca 2+ content. Phenylephrine depressed L-type current by around 30%. This effect was removed by blocking with 2-APB. Notably, phenylephrine failed to enhance the current, even in the presence of 2-APB. Furthermore, the phorbol ester, phorbol 12-myristate 13-acetate, had no effect on L-type current. Conclusion. Phenylephrine effects on the corpus cavernosum are mediated by modulation of the spontaneous pacemaker mechanism, rather than by direct stimulation of L-type channels.
机译:介绍。去甲肾上腺素在维持海绵体消肿音方面很重要,尽管其机理尚不完全清楚。由于L型Ca 2+通道阻滞剂拮抗了α-肾上腺素受体引起的音调,因此通常假定涉及该电流的直接调制。然而,从来没有直接检查过α-肾上腺素受体激动剂对海绵体肌细胞(CCSMC)中L型电流的影响,还有其他可能性。特别地,现在已知CCSMC通过起搏器机制产生自发的音调,该起搏器机制包括激活Cl-电流的自发Ca 2+波,从而引起L型通道的去极化和电压依赖性激活。我们假设去氧肾上腺素通过该系统而不是直接激活L型通道来调节音调。目的在新鲜分离的CCSMC中检查去氧肾上腺素对以下各项的影响:(i)自发的Cl-电流和去极化; (ii)胞质Ca 2+波; (iii)L型电流。方法。将CCSMC酶促分散于雄性新西兰白兔中以进行膜片钳记录和实时Ca 2+成像。主要观察指标。自发Cl-电流,自发去极化,胞质Ca 2+和L型电流。结果。苯肾上腺素增加了自发Cl-电流的幅度和频率,增加了自发去极化的持续时间和频率,并增加了自发Ca 2+波的频率。这些效应被2-氨基乙氧基二苯硼酸酯(2-APB)阻断,表明它们是由IP 3-诱导的Ca 2+从细胞内存储中释放而介导的。相反,2-APB对咖啡因释放储存的Ca 2+引起的Ca 2+瞬变没有影响,这表明它对储存的Ca 2+含量影响很小。苯肾上腺素抑制L型电流约30%。通过用2-APB阻断可以消除​​这种作用。值得注意的是,即使存在2-APB,去氧肾上腺素也不能增强电流。此外,佛波醇酯,佛波醇12-肉豆蔻酸酯13-乙酸酯,对L型电流没有影响。结论。苯肾上腺素对海绵体的作用是通过调节自发起搏器机制而不是通过直接刺激L型通道来介导的。

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