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钆和镉对离体大鼠神经垂体电诱发的45钙释放的影响。

Effects of gadolinium and cadmium on the electrically evoked release of 45calcium from the isolated rat neurohypophysis.

作者信息

Racké K, Hering B, Hochgesand U

机构信息

Department of Pharmacology, University of Mainz, Federal Republic of Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1988 Mar;337(3):301-7. doi: 10.1007/BF00168843.

Abstract

Isolated neural lobes of the rat pituitary gland were fixed by their stalks to a platinum wire electrode. They were loaded with 45calcium and then superfused with radioactivity-free Krebs-solution. The efflux of 45calcium into the superfusion medium was determined. After 54-60 min of superfusion the spontaneous outflow of 45calcium was 2.03%/min of the tissue 45calcium. It was not affected by cadmium (Cd2+, 0.03-3 mmol/l), but reduced by 40% in the presence of 1 mmol/l gadolinium (Gd3+). Electrical stimulation with pulses of 15 Hz (3 times for 1 min with intervals of 1 min) evoked a 45calcium release of 14.4% of the tissue radioactivity. The evoked release of 45calcium was reduced by 80% in the presence of tetrodotoxin and by about 50% in the presence of gallopamil (D600, 30 mumol/l) or after omission of unlabelled calcium from the superfusion medium. Gd3+ concentration-dependently reduced the evoked release by maximally 75% at 3 mmol/l. However, it inhibited the evoked release of 45calcium less effectively than the release of vasopressin evoked by identical stimulation conditions. Cd2+ reduced the evoked release by maximally 55% at 300 mumol/l. The effect of Cd2+ on the evoked release of vasopressin was not tested because Cd2+ markedly increased the spontaneous outflow of vasopressin. When the stimulation was carried out for only 1 min at 15 Hz (i.e. 900 pulses) the evoked release of 45calcium was 10.6% of the tissue 45calcium and 100 mumol/l Cd2+ or 300 mumol/l Gd3+ caused a reduction of the evoked release similar to that observed when 3 periods of stimulation were applied.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

将大鼠垂体的孤立神经叶通过其柄固定在铂丝电极上。给它们加载45钙,然后用无放射性的Krebs溶液进行灌流。测定45钙向灌流培养基中的流出量。灌流54 - 60分钟后,45钙的自发流出量为组织45钙的2.03%/分钟。它不受镉(Cd2 +,0.03 - 3 mmol/l)影响,但在存在1 mmol/l钆(Gd3 +)时减少40%。以15 Hz的脉冲进行电刺激(每次1分钟,共3次,间隔1分钟)可引起45钙释放量为组织放射性的14.4%。在存在河豚毒素时,45钙的诱发释放减少80%,在存在加洛帕米(D600,30 μmol/l)时或从灌流培养基中省略未标记钙后减少约50%。Gd3 +浓度依赖性地将诱发释放最大减少75%(在3 mmol/l时)。然而,与相同刺激条件下诱发的血管加压素释放相比,它对45钙诱发释放的抑制作用较小。Cd2 +在300 μmol/l时最大可将诱发释放减少55%。未测试Cd2 +对血管加压素诱发释放的影响,因为Cd2 +显著增加了血管加压素的自发流出量。当以15 Hz仅刺激1分钟(即900个脉冲)时,45钙的诱发释放量为组织45钙的10.6%,100 μmol/l Cd2 +或300 μmol/l Gd3 +导致诱发释放减少,类似于施加3个刺激周期时观察到的情况。(摘要截断于250字)

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