Gadek-Michalska A, Spyrka J, Bugajski J
Department of Physiology, Institute of Pharmacology, Polish Academy of Sciences, 12 Smetna Street, 31-343 Kraców, Poland.
J Physiol Pharmacol. 2005 Jun;56(2):287-98.
The role of prostaglandins and nitric oxide (NO), generated after peripheral lipopolysaccharide (LPS) administration, in the adaptation of hypothalamic-pituitary-adrenal (HPA) axis under stressful circumstances remains to be elucidated. The aim of the present study was to assess the effect of chronic repetitive restraint or social crowding stress on the involvement of nitric oxide and prostaglandins in the LPS-induced pituitary-adrenocortical response. Male Wistar rats were restrained in metal tubes 2 x 10 min/day or crowded in cages for 7 days prior to treatment. All compounds were injected i.p., cyclooxygenase (COX) and nitric oxide synthase (NOS) inhibitors 15 min before LPS. Two hrs after injection LPS induced a significant increase in ACTH and corticosterone secretion. Repeated restraint impaired more potently than crowding stress the LPS-induced HPA-response. Indomethacin, a non-selective COX inhibitor, considerably reduced the LPS-induced HPA response in non-stressed rats and to a lesser extent diminished this response in repeatedly restrained or crowded rats. Neuronal NOS inhibitor, Nomega-nitro-L-arginine decreased the LPS-induced HPA response, more potently in control than crowded rats. Aminoguanidine, an iNOS inhibitor, diminished the LPS-elicited ACTH response in crowded rats. These results indicate that prostaglandins and NO generated by neuronal and inducible NOS are involved in the LPS-induced HPA axis response under basal conditions and during its adaptation to chronic social stress circumstances.
外周给予脂多糖(LPS)后产生的前列腺素和一氧化氮(NO)在应激情况下对下丘脑-垂体-肾上腺(HPA)轴适应性的作用仍有待阐明。本研究的目的是评估慢性重复性束缚或社会拥挤应激对一氧化氮和前列腺素参与LPS诱导的垂体-肾上腺皮质反应的影响。雄性Wistar大鼠在治疗前每天被束缚在金属管中2×10分钟或在笼中拥挤7天。所有化合物均经腹腔注射,环氧合酶(COX)和一氧化氮合酶(NOS)抑制剂在注射LPS前15分钟给药。注射LPS两小时后,促肾上腺皮质激素(ACTH)和皮质酮分泌显著增加。重复性束缚比拥挤应激更有效地削弱了LPS诱导的HPA反应。非选择性COX抑制剂吲哚美辛在非应激大鼠中显著降低了LPS诱导的HPA反应,在重复性束缚或拥挤的大鼠中则在较小程度上减弱了这种反应。神经元型NOS抑制剂Nω-硝基-L-精氨酸降低了LPS诱导的HPA反应,在对照组大鼠中比在拥挤大鼠中更有效。诱导型NOS抑制剂氨基胍减弱了拥挤大鼠中LPS引发的ACTH反应。这些结果表明,由神经元型和诱导型NOS产生的前列腺素和NO在基础条件下及其适应慢性社会应激情况期间参与了LPS诱导的HPA轴反应。