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大鼠出生后对糖剥夺的低反应性。

Hyporesponsiveness to glucoprivation during postnatal period in the rat.

作者信息

Gil-Ad I, Udeschini G, Cocchi D, Müller E E

出版信息

Am J Physiol. 1975 Aug;229(2):512-7. doi: 10.1152/ajplegacy.1975.229.2.512.

Abstract

2-Deoxy-D-glucose (2-DG), a glucose analogue, blocks glycolysis and induces intracellular glucoprivation. In the adult rat intraperitoneal administration of 2-DG or its injection into the lateral ventricle (IVT) of the brain induces hyperglycemia which is divorced from a rise in plasma insulin (IRI). In the present study, responsiveness to 2-DG-induced glucoprivation, after central or intraperitoneal injection of the drug, was studied in rats of 7, 14, 21, and 28 days of age and compared to that of the adult rat (50 days old). In 7-, 14-, 21-, and 28-day-old rats, the overall blood glucose (BG) response to IVT-injected 2-DG was equivalent to 4, 3.3, 17, and 33%, respectively, of the BG response present in the adult rat. Following intraperitoneal injection of 2-DG , the BG response evoked in the same age groups corresponded to 27, 31, 41, and 93%, respectively, of the adult response. Base-line plasma IRI levels were significantly lower in pups than in adults and increased progressively with age, but no difference was present in IRI levels between 2-DG-treated and control pups whether the 2-DG was given via the laterl ventricle or intraperitoneally. These results demonstrate the presence in the infant rat of clear-cut hyporesponsiveness to 2-DG-induced glucoprivation. The different response pattern between experiments involving central and peripheral 2-DG administration supports the existence of separate peripheral glucoreceptors for 2-DG and their earlier ontogenic activation. Since the infant mammal glucose is of minor relevance as an energy substrate, an interrelationship appears to be present between requirements for fuel(s) and homeostatic response to fuel deprivation.

摘要

2-脱氧-D-葡萄糖(2-DG)是一种葡萄糖类似物,可阻断糖酵解并引发细胞内葡萄糖缺乏。在成年大鼠中,腹腔注射2-DG或将其注入脑侧脑室(IVT)会引发高血糖,且这种高血糖与血浆胰岛素(IRI)升高无关。在本研究中,对7、14、21和28日龄的大鼠进行中枢或腹腔注射该药物后,研究了其对2-DG诱导的葡萄糖缺乏的反应性,并与成年大鼠(50日龄)进行比较。在7、14、21和28日龄的大鼠中,IVT注射2-DG后总体血糖(BG)反应分别相当于成年大鼠BG反应的4%、3.3%、17%和33%。腹腔注射2-DG后,相同年龄组引发的BG反应分别相当于成年大鼠反应的27%、31%、41%和93%。幼崽的基线血浆IRI水平显著低于成年大鼠,且随年龄逐渐升高,但无论2-DG是通过侧脑室还是腹腔给药,2-DG处理组和对照组幼崽的IRI水平均无差异。这些结果表明幼鼠对2-DG诱导的葡萄糖缺乏存在明显的低反应性。涉及中枢和外周给予2-DG的实验之间不同的反应模式支持存在针对2-DG的独立外周葡萄糖受体及其更早的个体发生激活。由于幼年哺乳动物的葡萄糖作为能量底物的相关性较小,因此在燃料需求与对燃料剥夺的稳态反应之间似乎存在相互关系。

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