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首页> 外文期刊>Journal of Neurophysiology >Growth restriction induced by chronic prenatal hypoxia affects breathing rhythm and its pontine catecholaminergic modulation
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Growth restriction induced by chronic prenatal hypoxia affects breathing rhythm and its pontine catecholaminergic modulation

机译:慢性产前缺氧引起的生长受限影响呼吸节奏及其桥脑儿茶酚胺能调节

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摘要

Impaired transplacental supply of oxygen leads to intrauterine growth restriction, one of the most important causes of perinatal mortality and respiratory morbidity. Breathing rhythm depends on the central respiratory network modulated by catecholamines. We investigated the impact of growth restriction, using prenatal hypoxia, on respiratory frequency, on central respiratory-like rhythm, and on its catecholaminergic modulation after birth. At birth, respiratory frequency was increased and confirmed in en bloc medullary preparations, where the frequency of the fourth cervical (C4) ventral root discharge was increased, and in slice preparations containing the pre-Botzinger complex with an increased inspiratory rhythm. The inhibition of C4 burst discharge observed in pontomedullary preparations was stronger in the growth-restricted group. These results cannot be directly linked by the tyrosine hydroxylase activity increase of A(1)/C-1 and A(2)/C-2 cell groups in the medulla since blockade of alpha(1)- and alpha(2)-adrenergic receptors did not abolish the difference between both groups. However, in pontomedullary preparations, the stronger inhibition of C4 burst discharge is probably supported by an increased inhibition of A(5), a respiratory rhythm inhibitor pontine group of neurons displaying increased tyrosine hydroxylase activity, because blockade of alpha(2)-adrenergic receptors abolished the difference between the two groups. Taken together, these results indicate that growth restriction leads to a perturbation of the breathing frequency, which finds, at least in part, its origin in the modification of catecholaminergic modulation of the central breathing network.
机译:经胎盘供氧不足会导致子宫内生长受限,这是围产期死亡和呼吸系统疾病的最重要原因之一。呼吸节律取决于儿茶酚胺调节的中央呼吸网络。我们调查了使用产前低氧对呼吸频率,中枢呼吸样节律及其出生后儿茶酚胺能调节的生长限制的影响。出生时,整体髓样制剂中呼吸频率增加并得到确认,其中第四次宫颈(C4)腹侧根部分泌物的频率增加,并且在切片制剂中含有前Botzinger复合物且吸气节律增加。在生长受限的组中,在脑延髓制剂中观察到的对C4爆发放电的抑制作用更强。这些结果不能直接与髓质中A(1)/ C-1和A(2)/ C-2细胞组的酪氨酸羟化酶活性增加有关,因为对α(1)-和α(2)-肾上腺素的阻断受体并没有消除两组之间的差异。但是,在桥突准备中,对C4爆发放电的更强抑制可能是由于对A(5)的抑制作用得到了增强,A(5)是神经节律性酪氨酸羟化酶活性增强的神经元的呼吸节律抑制剂桥脑组,因为对α(2)-肾上腺素受体的阻断消除了两组之间的差异。综上所述,这些结果表明,生长受限导致呼吸频率的扰动,这至少部分地源于对中央呼吸网络的儿茶酚胺能调节的改变。

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