心房利钠因子(ANF)与促甲状腺素或生长抑素在甲状腺生长过程中的相互作用体外和离体研究。

Thyroidology Pub Date : 1994-12-01
P Biliński, A Lewiński, M Karbownik, M Klencki, E Wajs, J Kunert-Radek
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引用次数: 0

摘要

本研究的目的是研究心房利钠因子(ANF)对大鼠甲状腺叶生长过程的影响。体外实验初期,将甲状腺叶与大鼠ANF (Sigma)在含有3h -胸腺嘧啶(2微ci /ml)的RPMI 1640培养基中预孵育30 min,随后加入15%胎牛血清(FCS)、Hepes缓冲液和剩余被测物质[TSH 20 mIU/ml,生长抑素(SS) 10(-7)M]。在对照组和单独暴露于TSH的组中,未进行ANF预孵育。各实验组(对照组、单用TSH、单用ANF、ANF联合TSH或ANF联合SS)与3h -胸腺嘧啶孵育4小时。我们得到了以下结果:在检测浓度(10(-5)M, 10(-7)M, 10(-9)M)下,ANF都没有显著影响体外3h -胸腺嘧啶的掺入率。单独的TSH或与TSH联合的ANF都没有显著影响所讨论的过程。然而,我们观察到,与单独使用ANF相比,在甲状腺叶联合暴露于ANF (10(-7)M或10(-9)M)和SS (10(-7)M)后,3h -胸腺嘧啶摄取率增加。在离体实验中,将ANF单独或联合TSH或SS直接在甲状腺内进行显微注射。显微注射24小时后斩首处死,取甲状腺叶,用3h -胸腺嘧啶(2微ci /ml)孵育4小时。(摘要删节250字)
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Interactions between atrial natriuretic factor (ANF) and thyrotropin or somatostatin in their effects on thyroid growth processes; studies in vitro and ex vivo in vitro.

The goal of our present study has been to examine the effects of the atrial natriuretic factor (ANF) on the growth processes in rat thyroid lobes. In the initial in vitro experiment, thyroid lobes were preincubated with rat ANF (Sigma) for 30 min in RPMI 1640 medium with 3H-thymidine (2 microCi/ml), and later on 15% fetal calf serum (FCS), Hepes buffer and the remaining tested substances [TSH 20 mIU/ml, somatostatin (SS) 10(-7)M] were added. Preincubations with ANF were not conducted in the controls and in the group exposed to TSH alone. Incubations of all the examined groups (controls, TSH alone, ANF alone, ANF together with TSH or ANF together with SS) with 3H-thymidine were carried out for 4 hours. We obtained the following results: at none of the examined concentrations (10(-5)M, 10(-7)M, 10(-9)M), did ANF significantly affect the rate of 3H-thymidine incorporation in vitro. Neither did TSH alone nor ANF with TSH jointly significantly influence the process in question. However, we observed increased rates of the 3H-thymidine uptake, following the joint exposure of thyroid lobes to ANF (10(-7)M or 10(-9)M) and SS (10(-7)M), when compared to ANF alone. In the ex vivo in vitro experiment, direct intrathyroidal microinjections of ANF alone or jointly with TSH or SS, were carried out. Twenty four (24) hours after the microinjections, all the animals were sacrificed by decapitation, the thyroid lobes being collected and incubated for 4 hours with 3H-thymidine (2 microCi/ml).(ABSTRACT TRUNCATED AT 250 WORDS)

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