Anderson D L, Nelson J C, Haviland M G, MacMurray J P, Cummings M A, McGhee W H, Hubbard R W
Department of Psychiatry, Loma Linda University School of Medicine, CA 92350.
Psychiatry Res. 1992 Aug;43(2):121-8. doi: 10.1016/0165-1781(92)90126-n.
Thyroid stimulating hormone (TSH) and prolactin (PRL) responses to thyrotropin releasing hormone (TRH) stimulation are sometimes blunted in alcoholic subjects; however, the mechanisms involved in these phenomena have not been established. We hypothesized that elevations in free thyroid concentrations might be related to these abnormal responses and then tested that hypothesis in a sample of nondepressed alcoholic inpatients (n = 21). Four alcoholic patients had delta max TSH responses that were < 7 mIU/l; three had PRL responses at or below 8 micrograms/l. Baseline TSH was the only significant predictor of peak TSH; however, free thyroxine (FT4) and baseline TSH both were significant predictors of peak PRL. The average baseline FT4 concentration in alcoholic patients was significantly higher than that in healthy control subjects (n = 10). Our data, thus, suggest that small elevations of FT4 play a role in the inhibition of TSH and PRL responses to TRH among nondepressed, abstinent alcoholic patients.
在酒精摄入者中,促甲状腺激素(TSH)和催乳素(PRL)对促甲状腺激素释放激素(TRH)刺激的反应有时会减弱;然而,这些现象背后的机制尚未明确。我们推测游离甲状腺素浓度升高可能与这些异常反应有关,随后在一组未患抑郁症的酒精性疾病住院患者(n = 21)中对这一假设进行了验证。4名酒精性疾病患者的TSH最大变化量(delta max TSH)反应< 7 mIU/l;3名患者的PRL反应等于或低于8微克/升。基线TSH是TSH峰值的唯一显著预测因素;然而,游离甲状腺素(FT4)和基线TSH都是PRL峰值的显著预测因素。酒精性疾病患者的平均基线FT4浓度显著高于健康对照者(n = 10)。因此,我们的数据表明,在未患抑郁症、已戒酒的酒精性疾病患者中,FT4的小幅升高在抑制TSH和PRL对TRH的反应中发挥了作用。