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藜芦碱诱导大鼠输精管肾上腺素能神经释放3H-去甲肾上腺素的外向转运。

Veratridine-induced outward transport of 3H-noradrenaline from adrenergic nerves of the rat vas deferens.

作者信息

Bönisch H, Trendelenburg U

机构信息

Pharmakologisches Institut der Universität Würzburg, Federal Republic of Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1987 Dec;336(6):621-30. doi: 10.1007/BF00165752.

Abstract
  1. The neuronal release by 100 mumol/l veratridine of preloaded 3H-noradrenaline was studied in the rat vas deferens, the MAO, COMT and vesicular uptake of which were inhibited. To prevent any exocytotic release of the 3H-amine, all solutions were calcium-free. Veratridine induced an early and a late peak of tritium efflux. The early peak was abolished by the presence of 1 mumol/l desipramine, the late peak was abolished by 1 mumol/l tetrodotoxin (administered subsequently to the first peak). The administration of veratridine plus 1 mmol/l ouabain resulted in only the early peak of efflux. 2. The peak response to veratridine plus ouabain was increased by a very early administration of veratridine plus ouabain (after 40 min of wash-out instead of the usual 130 min) (i.e., when the relative size of the axoplasmic distribution compartment was increased). However, very high axoplasmic 3H-noradrenaline levels (after loading with 37 instead of the usual 0.2 mumol/l) reduced the height of the peak (when expressed as a FRL). 3. Substantially similar responses to veratridine plus ouabain were obtained after loading with 3H-noradrenaline, 3H-adrenaline or 3H-dopamine. 4. As the second peak of veratridine-induced release is ouabain-sensitive, it appears to be caused by exhaustion of neuronal ATP stores; this, in turn, raises the intravesicular pH and induces efflux of 3H-noradrenaline from the vesicles into the axoplasm. The first peak, on the other hand, represents outward transport of 3H-noradrenaline from the axoplasmic compartment. Evidently, a pronounced vesicular distribution of 3H-noradrenaline takes place even after inhibition by reserpine of the vesicular uptake. 5. In preparations with intact vesicular uptake (MAO and COMT inhibited) a plateau-response was obtained; in the presence of 10 mumol/l Ro 4-2184 (a reserpine-like compound) a peak response was restored after loading with 0.2 mumol/l 3H-noradrenaline, less so after loading with 37 mumol/l. 6. It is confirmed that veratridine (plus ouabain) exerts a reserpine-like effect when applied to tissues with intact vesicular uptake and intact MAO.
摘要
  1. 在大鼠输精管中研究了100μmol/L藜芦定对预加载的3H-去甲肾上腺素的神经元释放情况,该输精管的单胺氧化酶(MAO)、儿茶酚-O-甲基转移酶(COMT)和囊泡摄取均受到抑制。为防止3H-胺的任何胞吐释放,所有溶液均无钙。藜芦定诱导了氚外流的早期和晚期峰值。1μmol/L地昔帕明可消除早期峰值,1μmol/L河豚毒素(在第一个峰值后给药)可消除晚期峰值。给予藜芦定加1mmol/L哇巴因仅导致外流的早期峰值。2. 非常早期给予藜芦定加哇巴因(洗脱40分钟后而非通常的130分钟)(即当轴浆分布区室的相对大小增加时),对藜芦定加哇巴因的峰值反应增强。然而,非常高的轴浆3H-去甲肾上腺素水平(加载37μmol/L而非通常的0.2μmol/L后)会降低峰值高度(以FRL表示时)。3. 加载3H-去甲肾上腺素、3H-肾上腺素或3H-多巴胺后,对藜芦定加哇巴因的反应基本相似。4. 由于藜芦定诱导释放的第二个峰值对哇巴因敏感,似乎是由神经元ATP储备耗尽引起的;这反过来又提高了囊泡内pH值,并诱导3H-去甲肾上腺素从囊泡外流到轴浆中。另一方面,第一个峰值代表3H-去甲肾上腺素从轴浆区室的外向转运。显然,即使在利血平抑制囊泡摄取后,3H-去甲肾上腺素仍有明显的囊泡分布。5. 在囊泡摄取完整(MAO和COMT被抑制)的制剂中获得了平台反应;在存在10μmol/L Ro 4-2184(一种类似利血平的化合物)的情况下,加载0.2μmol/L 3H-去甲肾上腺素后恢复了峰值反应,加载37μmol/L后恢复程度较小。6. 已证实,当应用于囊泡摄取完整且MAO完整的组织时,藜芦定(加哇巴因)会产生类似利血平的作用。

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