首页> 美国卫生研究院文献>Journal of Young Pharmacists : JYP >Glucagon Secreting Cells Responds to Insulin Secretion In vitro Using Immunocytochemistry
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Glucagon Secreting Cells Responds to Insulin Secretion In vitro Using Immunocytochemistry

机译:胰高血糖素分泌细胞通过免疫细胞化学对胰岛素分泌进行体外反应

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摘要

In the present study, pancreas of rats were dissected and transferred to HEPES buffer (25 mM, pH 7.4). The control tissue pieces were kept in culture medium for one hour and the treated tissues were kept in same medium for 30 minutes and incubated with Insulin (10 nm and 100 nm) for another half hour, then tissues were transferred to Bouin‘s fixative (overnight at 40 ° Cc), cryosectioned (15 µm at -16 0 c) and subjected to immunocytochemical labeling with antibodies against Glucagon.Results:In the sections of control tissue, the Glucagon Immunoreactive Cells (GIC) were distinctly visible; on average 40-50 cells were counted in each islet. However in vitro treatment with 10 nm insulin caused 285.89 % increase in the GIC and was found to be highly significant (P< 0.001). Whereas in 100 nm Insulin treatment, 206.41% increase in GIC was seen, this was significant with the control but non-significant with 10 nm Insulin treatment
机译:在本研究中,解剖大鼠胰腺并将其转移至HEPES缓冲液(25 mM,pH 7.4)中。将对照组织块在培养基中放置1小时,将处理过的组织在相同培养基中放置30分钟,再与胰岛素(10 nm和100 nm)一起孵育半小时,然后将组织转移至Bouin's固定剂(结果:在对照组织切片中,清晰可见胰高血糖素免疫反应细胞(GIC);在40°C下过夜,在-16 0 c冷冻切片(在-16 0 c处15 µm)进行免疫细胞化学标记。每个胰岛平均计数40-50个细胞。然而,用10 nm胰岛素进行的体外治疗导致GIC升高285.89%,并且被发现具有显着意义(P <0.001)。在100 nm胰岛素治疗中,观察到GIC增加206.41%,这与对照组相比显着,但在10 nm胰岛素治疗中则无显着性

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