首页> 外文期刊>Stress: the international journal on the biology of stress >Acute stress or systemic insulin injection increases flunitrazepam sensitive-GABAA receptor density in synaptosomes of chick forebrain: Modulation by systemic epinephrine.
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Acute stress or systemic insulin injection increases flunitrazepam sensitive-GABAA receptor density in synaptosomes of chick forebrain: Modulation by systemic epinephrine.

机译:急性应激或全身性胰岛素注射会增加鸡前脑突触体中的氟尼西epa敏感型GABAA受体密度:全身性肾上腺素的调节。

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Interactions between acute stress and systemic insulin and epinephrine on GABAA receptor density in the forebrain were studied. Here, 10 day-old chicks were intraperitoneally injected with insulin, epinephrine or vehicle and then immediately stressed by partial water immersion for 15 min and killed by decapitation. Non-stressed controls were similarly injected, then returned to their rearing boxes for 15 min and then killed. Forebrains were dissected and GABAA receptor density was measured ex vivo in synaptosomes by 3[H]-flunitrazepam binding assay. In non-stressed chicks, insulin at 1.25, 2.50 and 5.00 IU/kg of body weight (non-hypoglycemic doses) increased Bmax by 33, 53 and 44% compared to saline, respectively. A similar increase of 41% was observed in receptor density after stress. However, the insulin effect was not additive to the stress-induced increase suggesting that both effects occur through similar mechanisms. In contrast, epinephrine, at 0.25 and 0.5 mg/kg did not induce any changes in Bmax in non-stressed chicks. Nevertheless, after stress these doses increased the receptor density by about 13 and 27%, respectively. Similarly, the same epinephrine doses co-administered with insulin (2.50 IU/kg), increased the receptor density by about 20% compared to insulin alone. These results suggest that systemic epinephrine, perhaps by evoking central norepinephrine release, modulates the increase in forebrain GABAA receptor binding induced by both insulin and stress.
机译:研究了急性应激与全身性胰岛素和肾上腺素对前脑GABA A受体密度的相互作用。在这里,给10日龄的小鸡腹膜内注射胰岛素,肾上腺素或媒介物,然后立即通过部分浸入水中15分钟使其紧张,并因断头而处死。相似地注射非应激对照,然后返回其饲养箱15分钟,然后杀死。解剖前脑并通过3 [H]-氟硝西epa结合测定离体测定突触体中的GABAA受体密度。在非应激雏鸡中,与盐水相比,以1.25、2.50和5.00 IU / kg体重的胰岛素(非降糖剂量)分别将Bmax升高33%,53%和44%。观察到应激后受体密度类似增加了41%。但是,胰岛素的作用并不能加重压力引起的增加,表明这两种作用都是通过相似的机制发生的。相反,肾上腺素在0.25和0.5 mg / kg时未引起未受压小鸡的Bmax的任何变化。然而,在应激后,这些剂量分别使受体密度增加了约13%和27%。类似地,与单独的胰岛素相比,相同的肾上腺素剂量与胰岛素共同给药(2.50 IU / kg)可使受体密度增加约20%。这些结果表明,全身性肾上腺素可能通过引起中央去甲肾上腺素的释放来调节胰岛素和应激诱导的前脑GABAA受体结合的增加。

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