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通过负离子质量碎片分析法测定氟西汀引起的脑内神经甾体含量变化。

Fluoxetine-elicited changes in brain neurosteroid content measured by negative ion mass fragmentography.

作者信息

Uzunov D P, Cooper T B, Costa E, Guidotti A

机构信息

Department of Psychiatry, University of Illinois at Chicago 60612, USA.

出版信息

Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12599-604. doi: 10.1073/pnas.93.22.12599.

Abstract

Fluoxetine administered intraperitoneally to sham-operated or adrenalectomized/castrated (ADX/CX) male rats dose-dependently (2.9-58 mumol/kg i.p.) increased the brain content of the neurosteroid 3 alpha-hydroxy-5 alpha-pregnan-20-one (allopregnanolone, 3 alpha, 5 alpha-TH PROG). The increase of brain 3 alpha, 5 alpha-TH PROG content elicited by 58 mumol/kg fluoxetine lasted more than 2 hr and the range of its extent was comparable in sham-operated (approximately 3-10 pmol/g) and ADX/CX rats (2-9 pmol/g) and was associated with a decrease (from 2.8 to 1.1 pmol/g) in the 5 alpha-pregnan-3,20-dione (5 alpha-dihydroprogesterone, 5 alpha-DH PROG) content. The pregnenolone, progesterone, and dehydroepiandrosterone content failed to change in rats receiving fluoxetine. The extent of 3 alpha, 5 alpha-TH PROG accumulation elicited by fluoxetine treatment differed in various brain regions, with the highest increase occurring in the olfactory bulb. Importantly, fluoxetine failed to change the 3 alpha, 5 alpha-TH PROG levels in plasma, which in ADX/CX rats were at least two orders of magnitude lower than in the brain. Two other serotonin re-uptake inhibitors, paroxetine and imipramine, in doses equipotent to those of fluoxetine in inhibiting brain serotonin uptake, were either significantly less potent than fluoxetine (paroxetine) or failed to increase (imipramine) 3 alpha, 5 alpha-TH PROG brain content. The addition of 10 microM of 5 alpha-DH PROG to brain slices of ADX/CX rats preincubated with fluoxetine (10 microM, 15 min) elicited an accumulation of 3 alpha, 5 alpha-TH PROG greater than in slices preincubated with vehicle. A fluoxetine stimulation of brain 3 alpha, 5 alpha-TH PROG biosynthesis might be operative in the anxiolytic and antidysphoric actions of this drug.

摘要

给假手术或肾上腺切除/阉割(ADX/CX)的雄性大鼠腹腔注射氟西汀,剂量依赖性地(2.9 - 58 μmol/kg腹腔注射)增加了神经甾体3α-羟基-5α-孕烷-20-酮(别孕烷醇酮,3α,5α-TH PROG)的脑内含量。58 μmol/kg氟西汀引起的脑内3α,5α-TH PROG含量增加持续超过2小时,其增加幅度在假手术大鼠(约3 - 10 pmol/g)和ADX/CX大鼠(2 - 9 pmol/g)中相当,并且与5α-孕烷-3,20-二酮(5α-双氢孕酮,5α-DH PROG)含量降低(从2.8降至1.1 pmol/g)相关。接受氟西汀的大鼠中孕烯醇酮、孕酮和脱氢表雄酮含量未发生变化。氟西汀治疗引起的3α,5α-TH PROG积累程度在不同脑区有所不同,嗅球中增加最为明显。重要的是,氟西汀未能改变血浆中3α,5α-TH PROG水平,在ADX/CX大鼠中,血浆中该水平比脑内至少低两个数量级。另外两种5-羟色胺再摄取抑制剂,帕罗西汀和丙咪嗪,在抑制脑内5-羟色胺摄取方面与氟西汀等效剂量时,要么效力明显低于氟西汀(帕罗西汀),要么未能增加(丙咪嗪)脑内3α,5α-TH PROG含量。在预先用氟西汀(10 μM,15分钟)孵育的ADX/CX大鼠脑片中加入10 μM的5α-DH PROG,引起的3α,5α-TH PROG积累比用溶剂孵育的脑片更大。氟西汀对脑内3α,5α-TH PROG生物合成的刺激作用可能在该药物的抗焦虑和抗烦躁作用中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5888/38038/6593d9af8cfb/pnas01526-0560-a.jpg

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