机构地区:[1]成都医学院体温与炎症四川省高校重点实验室,四川成都610500
出 处:《吉林大学学报(医学版)》2022年第6期1375-1381,共7页Journal of Jilin University:Medicine Edition
基 金:国家自然科学基金项目(31771289,32100926);成都医学院校基金项目(CYTD19-04);成都医学院研究生创新项目(YCX2021-08)。
摘 要:目的:探讨毁损臂旁外侧核(LPB)对大鼠脂多糖(LPS)致热反应的影响,阐明LPB是否参与LPS致热反应过程。方法:将12只雄性SD大鼠随机分为对照组和LPB毁损组,每组6只。采用核团注射的方法在LPB毁损组大鼠LPB局部注射鹅膏氨酸进行化学毁损,对照组大鼠注入等量生理盐水,恢复至少1周,腹腔植入监测体核温度(T_(core))所需的无线遥测发射子。采用无线遥控测温的方法监测2组大鼠腹腔注射生理盐水或LPS后不同时间点T_(core)和活动度,采用免疫荧光染色和尼氏染色法检测2组大鼠LPB中的NeuN和尼氏小体的分布。结果:对照组大鼠腹腔注射LPS(100μg·kg^(-1))后诱导出典型的双相发热,在腹腔注射LPS后1.5 h开始升温,2.5 h(1相)T_(core)首次达到峰值,3.5 h再次升温且5.5 h(2相)T_(core)第2次达到峰值;LPS毁损组大鼠腹腔注射LPS后也出现发热反应,5.5 h时T_(core)较基础T_(core)明显升高(P<0.05);与对照组比较,LPB毁损组大鼠发热反应明显减弱,腹腔注射LPS后2.5和5.5 h时T_(core)升高幅度均低于对照组(P<0.05)。对照组和LPS毁损组大鼠腹腔注射生理盐水或LPS后活动度均较注射前增加,但组间比较差异无统计学意义(P>0.05)。对照组大鼠LPB中分布大量NeuN免疫阳性神经元,尼氏小体大而数量多,细胞形态完整,边缘清晰;LPB毁损组大鼠头尾方向前、中和后3个水平的LPB毁损区域几乎未见NeuN免疫阳性神经元,神经元胞体缺失,尼氏小体大量消失。结论:LPB化学毁损模型部分消除了LPS的致热反应,表明LPB在LPS致热反应过程中起一定作用。Objective:To investigate the effect of lateral parabrachial(LPB)chemical lesion on the fever induced by lipopolysaccharide(LPS),and to clarify whether LPB was involved in the fever induced by LPS.Methods:Twelve adult male SD rats were randomly divided into control group and LPB-lesion group(n=6).The rats in LPB-lesion group were bilaterally injected with ibotenic acid into LPB by nuclear injection to induce chemical lession,and the rats in control group were injected with the equal amount of saline into LPB.The rats were survived for at least 1 week and then were implantated with telemetry transmitter for monitoring the body core temperature(T_(core))in the abdominal cavity.The T_(core) and activities of the rats in two groups at different time points after intraperitoneal injection of normal saline or LPS were monitored by radiotelemetry,and the distributions of NeuN and Nissl bodies in LPB of the rats in two groups were detected by immunofluorescence staining and Nissl staining.Results:The rats in control group were induced the typically biphasic fever after intraperitoneal injection of LPS(100μg·kg^(-1)),and the T_(core) started to rise 1.5 h after intraperitoneal injection of LPS,firstly reached its peak at 2.5 h(the first phase),started to rise again at 3.5 h and reached its peak again at 5.5 h(the second phase)after injection of LPS;the rats in LPB-lesion group also had fever reaction after intraperitoneal injection of LPS.At 5.5 h,the T_(core) was significantly higher than the basic T_(core)(P<0.05);compared with control group,the fever reaction of the rats in LPB-lesion group was significantly weakened,and the increasing of T_(core) at 2.5 and 5.5 h after intraperitoneal injection of LPS was lower than that in control group(P<0.05).After intraperitoneal injection of normal saline or LPS,the activities of the rats in control group and LPB-lesion group were increased temporarily compared with those before injection,but there were no significant differences between two groups(P>0.05).A large number of NeuN
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