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P物质在结状神经节/迷走神经外植体中的合成与转运:双结扎、2-脱氧葡萄糖、藜芦碱和哇巴因的影响

Substance P synthesis and transport in explants of nodose ganglion/vagus nerve: effects of double ligation, 2-deoxyglucose, veratridine, and ouabain.

作者信息

MacLean D B

出版信息

J Neurochem. 1987 Jun;48(6):1794-803. doi: 10.1111/j.1471-4159.1987.tb05738.x.

Abstract

Substance P (SP), the widely distributed undecapeptide, is synthesized in cell bodies of vagal sensory ganglia and transported bidirectionally toward the CNS and thoracic and abdominal viscera. In explants of the guinea pig inferior (nodose) vagal sensory ganglion and attached 2 cm of distal vagus nerve, SP is synthesized within the ganglion and transported predominantly distally. The quantity of distal transport is similar to that observed in vivo and provides an index of ongoing synthesis within the ganglion. In this report, the model is further characterized. Double ligation of the explant distal to the ganglion demonstrates that all the transported peptide is derived from the ganglion; there is no evidence of intraaxonal processing of peptide precursor. Approximately 50% of the peptide is in a rapid transport vs. an apparent stationary compartment. Not only transport, but also synthesis, of SP was blocked by 20 mM colchicine. Ongoing SP biosynthesis is dependent on a nutrient medium [medium 199 (M-199)] and is partially inhibited with added fetal bovine serum (FBS; 10%): total explant content in M-199/FBS vs. M-199, 1,785 +/- 101 (n = 8) vs. 2,254 +/- 123 pg (n = 9); p less than 0.02. Addition of 2-deoxyglucose (2-DG) decreased both total SP synthesis and transport (total explant content for 2-DG vs. control, 986 +/- 94 vs. 1,391 +/- 111; p less than 0.05). Medium supplemented with glucose to a final concentration of 600 mg/100 ml or with glucose (300 mg/100 ml) with or without insulin (50 ng/ml) did not alter explant SP content or transport. Veratridine (5 X 10(-6) M) inhibited both SP synthesis and transport; ouabain (10(-4) M) also inhibited synthesis, but less so transport. Tetrodotoxin reversed the effects of veratridine. These studies demonstrate the usefulness of this model, which can examine factors regulating both synthesis and transport of sensory neuropeptides in vitro. The results suggest that SP synthesis/transport may be under tonic inhibition, perhaps by both neural and humoral mechanisms.

摘要

P物质(SP)是一种广泛分布的十一肽,在迷走神经感觉神经节的细胞体中合成,并双向运输至中枢神经系统以及胸腹部内脏。在豚鼠迷走神经下(结状)感觉神经节及相连的2厘米远端迷走神经的外植体中,SP在神经节内合成并主要向远端运输。远端运输的量与体内观察到的相似,可作为神经节内持续合成的指标。在本报告中,对该模型进行了进一步的特性描述。在神经节远端对外植体进行双重结扎表明,所有运输的肽均来自神经节;没有证据表明肽前体存在轴突内加工。大约50%的肽处于快速运输与明显静止的区室中。20 mM秋水仙碱不仅阻断了SP的运输,还阻断了其合成。持续的SP生物合成依赖于营养培养基[199培养基(M-199)],添加胎牛血清(FBS;10%)会部分抑制其合成:M-199/FBS与M-199中的外植体总含量分别为1,785±101(n = 8)与2,254±123 pg(n = 9);p<0.02。添加2-脱氧葡萄糖(2-DG)会降低SP的总合成和运输(2-DG与对照的外植体总含量分别为986±94与1,391±111;p<0.05)。补充葡萄糖至最终浓度为600 mg/100 ml的培养基,或添加葡萄糖(300 mg/100 ml)且添加或不添加胰岛素(50 ng/ml)的培养基,均未改变外植体中SP的含量或运输。藜芦碱(5×10⁻⁶ M)抑制SP的合成和运输;哇巴因(10⁻⁴ M)也抑制合成,但对运输的抑制作用较小。河豚毒素可逆转藜芦碱的作用。这些研究证明了该模型的实用性,它可在体外研究调节感觉神经肽合成和运输的因素。结果表明,SP的合成/运输可能受到张力性抑制,可能是通过神经和体液机制。

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