Department of Legal Medicine, Osaka City University Medical School, Osaka, Japan.
Forensic Autopsy Section, Medico-legal Consultation and Postmortem Investigation Support Center (MLCPI-SC), Osaka, Japan.
PLoS One. 2020 Feb 18;15(2):e0218910. doi: 10.1371/journal.pone.0218910. eCollection 2020.
We previously showed that postmortem serum levels of adrenocorticotropic hormone (ACTH) were significantly higher in cases of hypothermia (cold exposure) than other causes of death. This study examined how the human hypothalamic-pituitary-adrenal axis, and specifically cortisol, responds to hypothermia. Human samples: Autopsies on 205 subjects (147 men and 58 women; age 15-98 years, median 60 years) were performed within 3 days of death. Cause of death was classified as either hypothermia (cold exposure, n = 14) or non-cold exposure (controls; n = 191). Cortisol levels were determined in blood samples obtained from the left and right cardiac chambers and common iliac veins using a chemiluminescent enzyme immunoassay. Adrenal gland tissues samples were stained for cortisol using a rabbit anti-human polyclonal antibody. Cell culture: AtT20, a mouse ACTH secretory cell line, and Y-1, a corticosterone secretory cell line derived from a mouse adrenal tumor, were analyzed in mono-and co-culture, and times courses of ACTH (in AtT20) and corticosterone (in Y-1) secretion were assessed after low temperature exposure mimicking hypothermia and compared with data for samples collected postmortem for other cases of death. However, no correlation between ACTH concentration and cortisol levels was observed in hypothermia cases. Immunohistologic analyses of samples from hypothermia cases showed that cortisol staining was localized primarily to the nucleus rather than the cytoplasm of cells in the zona fasciculata of the adrenal gland. During both mono-culture and co-culture, AtT20 cells secreted high levels of ACTH after 10-15 minutes of cold exposure, whereas corticosterone secretion by Y-1 cells increased slowly during the first 15-20 minutes of cold exposure. Similar to autopsy results, no correlation was detected between ACTH levels and corticosterone secretion, either in mono-culture or co-culture experiments. These results suggested that ACTH-independent cortisol secretion may function as a stress response during cold exposure.
我们之前的研究表明,低温(暴露于寒冷环境中)导致的尸检血清促肾上腺皮质激素(ACTH)水平明显高于其他死亡原因。本研究探讨了人类下丘脑-垂体-肾上腺轴,特别是皮质醇,对低温的反应。
对 205 例死亡 3 天内的尸检标本(男性 147 例,女性 58 例;年龄 15-98 岁,中位数 60 岁)进行了研究。死亡原因分为低温(暴露于寒冷环境,n=14)或非低温暴露(对照组,n=191)。使用化学发光酶免疫测定法,从左、右心房和髂总静脉采集血样,测定皮质醇水平。用兔抗人多克隆抗体对肾上腺组织样本进行皮质醇染色。
分析了 AtT20(一种分泌 ACTH 的小鼠细胞系)和 Y-1(一种源自小鼠肾上腺肿瘤的分泌皮质酮的细胞系)在单核和共培养中的情况,并在低温暴露(模拟低温)后评估了 ACTH(在 AtT20 中)和皮质酮(在 Y-1 中)的分泌时程,并与其他死亡病例的尸检样本数据进行了比较。然而,在低温病例中,并未观察到 ACTH 浓度与皮质醇水平之间的相关性。低温病例样本的免疫组织化学分析表明,皮质醇染色主要定位于肾上腺束状带细胞的细胞核,而不是细胞质。在单核和共培养中,AtT20 细胞在低温暴露 10-15 分钟后分泌大量 ACTH,而 Y-1 细胞的皮质酮分泌在低温暴露的最初 15-20 分钟内缓慢增加。与尸检结果类似,无论是在单核培养还是共培养实验中,均未检测到 ACTH 水平与皮质酮分泌之间的相关性。这些结果表明,ACTH 非依赖性皮质醇分泌可能在低温暴露期间作为应激反应发挥作用。