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尼古丁和睡眠剥夺:对大鼠疼痛敏感性和免疫调节的影响。

Nicotine and sleep deprivation: impact on pain sensitivity and immune modulation in rats.

机构信息

Department of Psychobiology, Universidade Federal de São Paulo, São Paulo, Brazil.

Department of Psychiatry and Human Behavior, University of Mississippi Medical Center, Jackson, USA.

出版信息

Sci Rep. 2018 Sep 14;8(1):13837. doi: 10.1038/s41598-018-32276-7.

Abstract

Repeated nicotine administration has been associated with increased paradoxical sleep in rats and antinociceptive properties, whereas paradoxical sleep deprivation (PSD) elicits pronociceptive and inflammatory responses. Thus, we aimed to evaluate the effect of repeated nicotine administration and its withdrawal combined with PSD on pain sensitivity and inflammatory markers. Sixty adult male Wistar rats were subjected to repeated injections of saline (SAL) or nicotine (NIC) for 12 days or 7 days of nicotine followed by acute mecamylamine administration on day 8 to precipitate nicotine abstinence (ABST). On day 9, the animals were submitted to PSD for 72 h or remained in control condition (CTRL); on day 12, thermal pain threshold was assessed by the hot plate test. PSD significantly decreased the latency to paw withdrawal in all groups compared to their respective controls. ABST-PSD animals presented higher levels of interleukin (IL)-6 compared to all groups, except ABST-CTRL. After adjustment for weight loss, IL-6, IL-4 and tumor necrosis factor alpha, ABST-PSD was associated with the lowest pain threshold. Nicotine and IL-4 levels were predictors of higher pain threshold. Hyperalgesia induced by PSD prevailed over the antinociceptive action of nicotine, while the association between PSD and ABST synergistically increased IL-6 concentrations and decreased pain threshold.

摘要

重复给予尼古丁会导致大鼠的异相睡眠增加和镇痛作用,而异相睡眠剥夺(PSD)会引发痛觉敏化和炎症反应。因此,我们旨在评估重复给予尼古丁及其戒断与 PSD 联合对疼痛敏感性和炎症标志物的影响。将 60 只成年雄性 Wistar 大鼠分为盐水(SAL)组或尼古丁(NIC)组,连续 12 天给予 SAL 或 NIC 注射,或连续 7 天给予 NIC 注射,然后在第 8 天给予美加明以诱发尼古丁戒断(ABST)。第 9 天,动物进行 72 小时 PSD 或保持对照条件(CTRL);第 12 天,通过热板试验评估热痛阈值。与各自的对照组相比,PSD 显著降低了所有组的爪子回缩潜伏期。与所有组相比,ABST-PSD 组的白细胞介素(IL)-6 水平更高,除了 ABST-CTRL 组。在调整体重减轻、IL-6、IL-4 和肿瘤坏死因子α后,ABST-PSD 与最低的痛阈值相关。尼古丁和 IL-4 水平是较高痛阈值的预测因子。PSD 引起的痛觉过敏超过了尼古丁的镇痛作用,而 PSD 和 ABST 的联合作用则协同增加了 IL-6 浓度并降低了痛阈值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1161/6138689/2dfb7ee24f06/41598_2018_32276_Fig1_HTML.jpg

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