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ICI 182,780可穿透脑和下丘脑组织,全身给药后在脑中具有功能效应。

ICI 182,780 penetrates brain and hypothalamic tissue and has functional effects in the brain after systemic dosing.

作者信息

Alfinito Peter D, Chen Xiaohong, Atherton James, Cosmi Scott, Deecher Darlene C

机构信息

Women's Health and Musculoskeletal Biology, Wyeth Research, RN 3164, 500 Arcola Road, Collegeville, Pennsylvania 19426, USA.

出版信息

Endocrinology. 2008 Oct;149(10):5219-26. doi: 10.1210/en.2008-0532. Epub 2008 Jul 3.

Abstract

Previous reports suggest the antiestrogen ICI 182,780 (ICI) does not cross the blood-brain barrier (BBB). However, this hypothesis has never been directly tested. In the present study, we tested whether ICI crosses the BBB, penetrates into brain and hypothalamic tissues, and affects known neuroendocrine functions in ovariectomized rats. Using HPLC with mass spectrometry, ICI (1.0 mg/kg.d, 3 d) was detected in plasma and brain and hypothalamic tissues for up to 24 h with maximum concentrations of 43.1 ng/ml, and 31.6 and 38.8 ng/g, respectively. To evaluate antiestrogenic effects of ICI in the brain after systemic dosing, we tested its ability to block the effect of 17 alpha-ethinyl estradiol (EE) (0.3 mg/kg, 8 d) on tail-skin temperature abatement in the morphine-dependent model of hot flush and on body weight change. In the morphine-dependent model, EE abated 64% of the naloxone-induced tail-skin temperature increase. ICI pretreatment (1.0, 3.0 mg/kg.d) dose dependently inhibited this effect. ICI (3.0 mg/kg.d) alone showed estrogenic-like actions, abating 30% the naloxone-induced flush. In body weight studies, EE-treated rats weighed 58.5 g less than vehicle-treated rats after 8 d dosing. This effect was partially blocked by ICI (3.0 mg/kg.d) pretreatment. Similar to EE treatment, rats receiving 1.0 or 3.0 mg/kg.d ICI alone showed little weight gain compared with vehicle-treated controls. Thus, ICI crosses the BBB, penetrates into brain and hypothalamic tissues, and has both antiestrogenic and estrogenic-like actions on neuroendocrine-related functions.

摘要

先前的报告表明,抗雌激素药物ICI 182,780(ICI)无法穿过血脑屏障(BBB)。然而,这一假设从未得到直接验证。在本研究中,我们检测了ICI是否能穿过血脑屏障、渗透至脑和下丘脑组织,并影响去卵巢大鼠已知的神经内分泌功能。采用高效液相色谱-质谱联用技术,在血浆、脑和下丘脑组织中检测到ICI(1.0毫克/千克·天,共3天),长达24小时,其最大浓度分别为43.1纳克/毫升、31.6纳克/克和38.8纳克/克。为了评估全身给药后ICI在脑中的抗雌激素作用,我们检测了其在吗啡依赖的潮热模型中阻断17α-乙炔雌二醇(EE)(0.3毫克/千克,共8天)对尾皮温度降低作用以及对体重变化的能力。在吗啡依赖模型中,EE减轻了64%的纳洛酮诱导的尾皮温度升高。ICI预处理(1.0、3.0毫克/千克·天)呈剂量依赖性地抑制了这一作用。单独使用ICI(3.0毫克/千克·天)表现出类似雌激素的作用,减轻了30%的纳洛酮诱导的潮热。在体重研究中,给药8天后,接受EE治疗的大鼠比接受赋形剂治疗的大鼠体重轻58.5克。ICI(3.0毫克/千克·天)预处理部分阻断了这一作用。与EE治疗相似,单独接受1.0或3.0毫克/千克·天ICI治疗的大鼠与接受赋形剂治疗的对照组相比体重增加很少。因此,ICI能穿过血脑屏障,渗透至脑和下丘脑组织,并对神经内分泌相关功能具有抗雌激素和类似雌激素的作用。

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