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肾上腺中2-[125I]碘褪黑素的结合位点。

Binding sites for 2-[125I]iodomelatonin in the adrenal gland.

作者信息

Brown G M, Pang C S, Pang S F

机构信息

Clarke Institute of Psychiatry, Toronto, Canada.

出版信息

Biol Signals. 1994 Mar-Apr;3(2):91-8. doi: 10.1159/000109530.

DOI:10.1159/000109530
PMID:7951652
Abstract

The existence of melatonin receptors in adrenal glands is suggested by effects on rodent adrenal function which follow pinealectomy or in vivo and in vitro melatonin treatment. In 1992, Persengiev and coworkers reported specific binding of 2-[125I]iodomelatonin to rat adrenal tissue. In order to study adrenal binding further we have done binding studies on adrenal membranes from ducks sacrificed at midlight. We observed binding of 2-[125I]iodomelatonin which was specific, rapid, saturable, stable, reversible and of high affinity. Scatchard plots were linear and Hill coefficients were close to unity supporting the existence of a single class of 2-[125I]iodomelatonin binding sites. On Scatchard analysis the Kd was in the physiological range (27.4 pmol/l) together with a Bmax of 3.38 fmol/mg protein. Sites were highly specific to melatonin and its two synthetic analogs, 2-iodomelatonin and 6-chloromelatonin in pharmacological studies. In autoradiographic studies on the chicken adrenal gland, one class of 2-[125I]iodomelatonin binding site was demonstrated with a Kd of 58.8 pmol/l and Bmax of 182 fmol/g tissue. Kinetic and pharmacological studies indicated that these sites are saturable, reversible, and of high specificity and affinity. These findings in the chicken are similar to those of the duck adrenal data obtained by radioreceptor assay. In preliminary studies, no significant difference was found between 2-[125I]iodomelatonin binding to the adrenal glands collected at midlight and middark. These high-affinity binding sites are similar to those reported in a wide variety of tissues and are consistent with the hypothesis of direct action of melatonin on the adrenal gland.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

松果体切除术后或体内及体外褪黑素治疗对啮齿动物肾上腺功能产生的影响提示肾上腺中存在褪黑素受体。1992年,佩尔森吉耶夫及其同事报告了2-[¹²⁵I]碘褪黑素与大鼠肾上腺组织的特异性结合。为了进一步研究肾上腺结合情况,我们对处于光照中期处死的鸭子的肾上腺膜进行了结合研究。我们观察到2-[¹²⁵I]碘褪黑素的结合具有特异性、快速、可饱和、稳定、可逆且亲和力高的特点。斯卡查德图呈线性,希尔系数接近1,支持存在一类单一的2-[¹²⁵I]碘褪黑素结合位点。经斯卡查德分析,解离常数处于生理范围内(27.4皮摩尔/升),最大结合容量为3.38飞摩尔/毫克蛋白质。在药理学研究中,这些位点对褪黑素及其两种合成类似物2-碘褪黑素和6-氯褪黑素具有高度特异性。在鸡肾上腺的放射自显影研究中,证实存在一类2-[¹²⁵I]碘褪黑素结合位点,解离常数为58.8皮摩尔/升,最大结合容量为182飞摩尔/克组织。动力学和药理学研究表明,这些位点是可饱和、可逆的,且具有高度特异性和亲和力。鸡的这些发现与通过放射受体测定法获得的鸭肾上腺数据相似。在初步研究中,未发现处于光照中期和黑暗中期收集的肾上腺对2-[¹²⁵I]碘褪黑素的结合有显著差异。这些高亲和力结合位点与在多种组织中报道的位点相似,与褪黑素对肾上腺直接作用的假说一致。(摘要截短于250字)

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Binding sites for 2-[125I]iodomelatonin in the adrenal gland.肾上腺中2-[125I]碘褪黑素的结合位点。
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