Jutkiewicz Emily M, Wood Susan K, Houshyar Hani, Hsin Ling-Wei, Rice Kenner C, Woods James H
Department of Pharmacology, University of Michigan Medical School, 1301 MSRB 3, Ann Arbor, MI 48109-0632, USA.
Psychopharmacology (Berl). 2005 Jul;180(2):215-23. doi: 10.1007/s00213-005-2164-z. Epub 2005 Feb 5.
Exposure to extreme stress has been suggested to produce long-term, detrimental alterations in the hypothalamic-pituitary-adrenal (HPA) axis leading to the development of mental disorders such as depression. Therefore, compounds that block the effects of stress hormones were investigated as potential therapeutics for depression.
In the present study, we compared the potential antidepressant-like effects of four CRF antagonists, antalarmin, CP154,526, R121919, and LWH234 (at 3, 10, and 30 mg/kg i.p., 60 min prior to the forced swim test) and the corresponding effect on swim-induced HPA activation to better elucidate the relation between HPA activity and antidepressant activity.
The antidepressant-like effects of the CRF antagonists and known antidepressants were determined in the rat forced swim test, and blood samples were obtained before and after swimming for the evaluation of adrenocorticotropin-releasing hormone (ACTH) levels.
Antalarmin, CP154,526, and R121919 did not produce antidepressant-like effects in the forced swim test although these compounds decreased swim-induced increases in ACTH to various extents. In contrast, LWH234 reduced immobility in the forced swim test, without altering the swim-stress-induced ACTH response. However, this compound antagonized restraint-induced ACTH release.
These data suggest that reducing stress-induced increases in HPA activity alone may not be sufficient to produce antidepressant-like activity; however, reductions in HPA activity may contribute to antidepressant actions of some treatments. In addition, it is proposed that CRF antagonists may alter differentially the HPA axis depending on the type of stressor used or behavioral measure evaluated.
有研究表明,暴露于极端压力会导致下丘脑 - 垂体 - 肾上腺(HPA)轴发生长期的有害改变,进而引发抑郁症等精神障碍。因此,人们对能够阻断应激激素作用的化合物作为抑郁症潜在治疗药物进行了研究。
在本研究中,我们比较了四种促肾上腺皮质激素释放因子(CRF)拮抗剂,即安他拉美、CP154526、R121919和LWH234(腹腔注射,剂量分别为3、10和30mg/kg,在强迫游泳试验前60分钟给药)的潜在抗抑郁样作用,以及它们对游泳诱导的HPA激活的相应影响,以更好地阐明HPA活性与抗抑郁活性之间的关系。
在大鼠强迫游泳试验中测定CRF拮抗剂和已知抗抑郁药的抗抑郁样作用,并在游泳前后采集血样以评估促肾上腺皮质激素释放激素(ACTH)水平。
安他拉美、CP154526和R121919在强迫游泳试验中未产生抗抑郁样作用,尽管这些化合物在不同程度上降低了游泳诱导的ACTH升高。相比之下,LWH234减少了强迫游泳试验中的不动时间,且未改变游泳应激诱导的ACTH反应。然而,该化合物拮抗了束缚诱导的ACTH释放。
这些数据表明,仅降低应激诱导的HPA活性增加可能不足以产生抗抑郁样活性;然而,HPA活性的降低可能有助于某些治疗的抗抑郁作用。此外,有人提出CRF拮抗剂可能根据所使用的应激源类型或所评估的行为指标不同程度地改变HPA轴。