Pham Grace S, Mathis Keisa W
Department of Physiology and Anatomy, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.
Brain Sci. 2018 Oct 4;8(10):184. doi: 10.3390/brainsci8100184.
Crosstalk between the brain and innate immune system may be dysregulated in systemic lupus erythematosus (SLE), a chronic autoimmune disease that presents with dysautonomia and aberrant inflammation. The hypothalamic-pituitary-adrenal (HPA) axis is an endogenous neuro-endocrine-immune pathway that can regulate inflammation following activation of vagal afferents. We hypothesized that chronic inflammatory processes in SLE are in part due to HPA axis dysfunction, at the level of either the afferent vagal-paraventricular nuclei (PVN) interface, the anterior pituitary, and/or at the adrenal glands. To study this, we challenged female control and SLE mice with lipopolysaccharide (LPS) and measured c-Fos expression as an index of neuronal activation, plasma adrenocorticotrophic hormone (ACTH) as an index of anterior pituitary function, and plasma corticosterone as an index of adrenal function. We found that c-Fos expression in the PVN, and plasma ACTH and corticosterone were comparable between unchallenged SLE and control mice. PVN c-Fos was increased similarly in control and SLE mice three hours after LPS challenge; however, there were no changes in plasma ACTH amongst any experimental groups post inflammatory challenge. Plasma corticosterone was markedly increased in LPS-challenged SLE mice compared to their vehicle-treated counterparts, but not in controls. Paradoxically, following LPS challenge, brain and spleen TNF-α were elevated in LPS-challenged SLE mice despite heightened plasma corticosterone. This suggests that, despite normal c-Fos expression in the PVN and activation of the HPA axis following LPS challenge, this cumulative response may not adequately defend SLE mice against inflammatory stimuli, leading to abnormally heightened innate immune responses and peripheral inflammation.
大脑与先天免疫系统之间的串扰在系统性红斑狼疮(SLE)中可能失调,这是一种慢性自身免疫性疾病,伴有自主神经功能障碍和异常炎症。下丘脑-垂体-肾上腺(HPA)轴是一条内源性神经-内分泌-免疫途径,可在迷走神经传入纤维激活后调节炎症。我们假设,SLE中的慢性炎症过程部分归因于HPA轴功能障碍,其发生在传入迷走神经-室旁核(PVN)界面、垂体前叶和/或肾上腺水平。为了研究这一点,我们用脂多糖(LPS)刺激雌性对照小鼠和SLE小鼠,并测量c-Fos表达作为神经元激活指标、血浆促肾上腺皮质激素(ACTH)作为垂体前叶功能指标以及血浆皮质酮作为肾上腺功能指标。我们发现,未受刺激的SLE小鼠和对照小鼠之间,PVN中的c-Fos表达、血浆ACTH和皮质酮水平相当。LPS刺激后3小时,对照小鼠和SLE小鼠的PVN中c-Fos同样增加;然而,炎症刺激后任何实验组的血浆ACTH均无变化。与接受赋形剂处理的SLE小鼠相比,LPS刺激的SLE小鼠血浆皮质酮显著增加,但对照小鼠未出现这种情况。矛盾的是,LPS刺激后,尽管血浆皮质酮升高,但LPS刺激的SLE小鼠的大脑和脾脏TNF-α却升高。这表明,尽管LPS刺激后PVN中c-Fos表达正常且HPA轴激活,但这种累积反应可能无法充分保护SLE小鼠免受炎症刺激,导致先天免疫反应和外周炎症异常增强。