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甲状旁腺素相关蛋白抑制豚鼠胃窦平滑肌收缩的机制。

Mechanisms of PTHrP-induced inhibition of smooth muscle contractility in the guinea pig gastric antrum.

机构信息

Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Department of Cell Physiology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

出版信息

Neurogastroenterol Motil. 2017 Dec;29(12). doi: 10.1111/nmo.13142. Epub 2017 Jun 28.

Abstract

BACKGROUND

Parathyroid hormone-related protein (PTHrP) that causes hypercalcemia of malignancy appears to function as an endogenous smooth muscle relaxant. For example, PTHrP released upon bladder wall distension relaxes detrusor smooth muscle to accommodate urine. Here, we explored mechanisms underlying PTHrP-induced suppression of the smooth muscle contractility in the gastric antrum that also undergoes a passive distension.

METHODS

Effects of PTHrP on phasic contractions and electrical slow waves in the antral smooth muscle of the guinea pig stomach were studied using isometric tension and intracellular microelectrode recordings, respectively. Fluorescent immunohistochemistry was also carried out to identify the distribution of PTH/PTHrP receptors.

KEY RESULTS

Parathyroid hormone-related protein (1-100 nM) reduced the amplitude of phasic contractions and the basal tension. N -nitro-l-arginine (L-NA, 100 μM), a nitric oxide (NO) synthase inhibitor, or 1H-[1,2,4]oxadiazolo-[4, 3-a]quinoxalin-1-one (ODQ, 10 µM), a guanylate cyclase inhibitor, diminished the PTHrP (10 nM)-induced reduction in the amplitude of phasic contractions. SQ22536 (300 μM), an adenylate cyclase inhibitor, attenuated the PTHrP-induced reduction in basal tension. The combination of ODQ (10 μM) and SQ22536 (300 μM) inhibited the PTHrP-induced reductions in both phasic contractions and basal tension. PTHrP (100 nM) had no inhibitory effect on the electrical slow waves in the antral smooth muscle. PTH/PTHrP receptors were expressed in cell bodies of PGP9.5-positive neurons in the myenteric plexus.

CONCLUSIONS & INFERENCES: Parathyroid hormone-related protein exerts its inhibitory actions on the antral smooth muscle via both nitric oxide-cyclic guanosine monophosphate (NO-cGMP) and cyclic adenosine monophosphate (AMP) pathways. Thus, PTHrP may act as an endogenous relaxant of the gastric antrum employing the two complementary signaling pathways to ensure the adaptive relaxation of stomach.

摘要

背景

甲状旁腺激素相关蛋白(PTHrP)引起的恶性肿瘤高钙血症似乎作为一种内源性平滑肌松弛剂发挥作用。例如,在膀胱壁扩张时释放的 PTHrP 可使逼尿肌平滑肌松弛以容纳尿液。在这里,我们探讨了 PTHrP 诱导胃窦平滑肌收缩抑制的机制,胃窦平滑肌也经历被动扩张。

方法

使用等长张力和细胞内微电极记录分别研究了 PTHrP 对豚鼠胃窦平滑肌的相位收缩和电慢波的影响。还进行了荧光免疫组织化学以鉴定 PTH/PTHrP 受体的分布。

主要结果

甲状旁腺激素相关蛋白(1-100 nM)降低了相位收缩的幅度和基础张力。一氧化氮(NO)合酶抑制剂 N-硝基-L-精氨酸(L-NA,100 μM)或鸟苷酸环化酶抑制剂 1H-[1,2,4]恶二唑-[4,3-a]喹喔啉-1-酮(ODQ,10 μM)减弱了 PTHrP(10 nM)诱导的相位收缩幅度降低。腺嘌呤核苷酸环化酶抑制剂 SQ22536(300 μM)减弱了 PTHrP 诱导的基础张力降低。ODQ(10 μM)和 SQ22536(300 μM)的组合抑制了 PTHrP 诱导的相位收缩和基础张力降低。PTHrP(100 nM)对胃窦平滑肌的电慢波没有抑制作用。PTH/PTHrP 受体存在于肌间神经丛中 PGP9.5 阳性神经元的细胞体中。

结论和推论

甲状旁腺激素相关蛋白通过一氧化氮-环鸟苷酸(NO-cGMP)和环腺苷酸(AMP)途径发挥对胃窦平滑肌的抑制作用。因此,PTHrP 可能作为胃窦的内源性松弛剂,利用两种互补的信号通路来确保胃的适应性松弛。

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