CAJ | 학술논문

目的探讨在创伤后应激障碍(PTSD)状态下脊髓谷氨酸转运体-1(GLT-1)表达的改变及GLT-1激动剂头孢曲松钠(CTX)抗内脏伤害性刺激的作用.方法 SD大鼠分为5组:生理盐水对照组、PTSD内脏高敏感模型组、CTX预处理组、PTSD+CTX组及PTSD+CTX+二氢卡因酸盐(DHK)组.每组7只鼠用于内脏敏感性测定,均最终完成试验;每组10只鼠用于GLT-1免疫荧光检测,最终分别有8、9、8、10、7只完成试验.采用腹腔注射卵清蛋白(OVA)基础致敏联合连续单一应激(SPS)建立PTSD内脏高敏感大鼠模型;建模后7d采用结直肠扩张(CRD)-内脏运动反射(VMR)评估PTSD状态下内脏敏感性改变;采用CTX选择性诱发编码GLT-1的基因转录及上调GLT-1的表达;采用免疫荧光及激光共聚焦显微技术研究脊髓GLT-1蛋白表达水平的变化.结果与正常对照组比较,CTX组大鼠脊髓背角GLT-1表达水平较高,吸光度(A)值显著高于正常对照组(141.38±2.91比106.25±3.32,P=0.001),而PTSD组则明显低于正常对照组(86.11±2.73比106.25±3.32,P=0.001);PTSD+ CTX组GLT-1的表达亦高于PTSD组(98.70±3.19比86.11±2.73,P=0.004).在20、40、60、80 mmHg(1 mmHg =0.133 kPa)压力下行CRD,术后7 d PTSD组在各压力水平下的VMR曲线下面积(AUCVMR)均显著高于正常对照组(P值均＜0.05);PTSD+ CTX组在各压力水平的AUCVMR明显低于PTSD组(P值均＜0.01);在80 mmHg行伤害性内脏刺激时,GLT-1抑制剂DHK可逆转CTX的抗伤害刺激效应(P =0.002).在40、60、80 mmHg下行CRD时,CTX组的AUCvMR明显低于正常对照组(P值均＜0.05).结论腹腔注射OVA基础致敏联合SPS可成功建立PTSD内脏高敏感大鼠模型.在PTSD内脏高敏感状态下,CTX可通过上调脊髓GLT-1的表达发挥抗内脏伤害性刺激的作用,可能成为防止或抑制PTSD状态下内脏高敏感性-痛觉敏化新的靶点之一.
목적 탐토재창상후응격장애(PTSD)상태하척수곡안산전운체-1(GLT-1)표체적개변급GLT-1격동제두포곡송납(CTX)항내장상해성자격적작용.방법 SD대서분위5조:생리염수대조조、PTSD내장고민감모형조、CTX예처리조、PTSD+CTX조급PTSD+CTX+이경잡인산염(DHK)조.매조7지서용우내장민감성측정,균최종완성시험;매조10지서용우GLT-1면역형광검측,최종분별유8、9、8、10、7지완성시험.채용복강주사란청단백(OVA)기출치민연합련속단일응격(SPS)건립PTSD내장고민감대서모형;건모후7d채용결직장확장(CRD)-내장운동반사(VMR)평고PTSD상태하내장민감성개변;채용CTX선택성유발편마GLT-1적기인전록급상조GLT-1적표체;채용면역형광급격광공취초현미기술연구척수GLT-1단백표체수평적변화.결과 여정상대조조비교,CTX조대서척수배각GLT-1표체수평교고,흡광도(A)치현저고우정상대조조(141.38±2.91비106.25±3.32,P=0.001),이PTSD조칙명현저우정상대조조(86.11±2.73비106.25±3.32,P=0.001);PTSD+ CTX조GLT-1적표체역고우PTSD조(98.70±3.19비86.11±2.73,P=0.004).재20、40、60、80 mmHg(1 mmHg =0.133 kPa)압력하행CRD,술후7 d PTSD조재각압력수평하적VMR곡선하면적(AUCVMR)균현저고우정상대조조(P치균＜0.05);PTSD+ CTX조재각압력수평적AUCVMR명현저우PTSD조(P치균＜0.01);재80 mmHg행상해성내장자격시,GLT-1억제제DHK가역전CTX적항상해자격효응(P =0.002).재40、60、80 mmHg하행CRD시,CTX조적AUCvMR명현저우정상대조조(P치균＜0.05).결론 복강주사OVA기출치민연합SPS가성공건립PTSD내장고민감대서모형.재PTSD내장고민감상태하,CTX가통과상조척수GLT-1적표체발휘항내장상해성자격적작용,가능성위방지혹억제PTSD상태하내장고민감성-통각민화신적파점지일.
Objective To investigate the expression of glutamate transporter 1 (GLT-1) and determine the effect of GLT-1 overexpression on the viscemmotor response (VMR) to colorectal distention (CRD) following exposure to post-traumatic stress disorder (PTSD)-like stress.Methods A beta-lactam antibiotic,ceftriaxone (CTX) was used to selectively induce transcription of the gene encoding GLT-1 and upregulate GLT-1 expression as an agonist.SD rats were divided into five groups,including control group,PTSD group,CTX-treated group,PTSD + CTX group,PTSD + CTX + dihydrokainate (DHK) group.Seven rats in each VMR-CRD group eventually completed the study.Ten rats in each group were used to test immunofluorescence of GLT-1,however,8,9,8,10,7 rats completed the test respectively.The animal model of PTSD was established using basal ovalbumin (OVA)-sensitization combined with single-prolonged stress model (SPS).The alteration of visceral sensitivity following exposure to PTSD-like stress was evaluated by measuring the VMR to CRD.Spinal GLT-1 expression was evaluated by immunofluorescence using confocal laser scanning microscopy.Results By immunofluorescence analysis,CTX-treated rats exhibited an increased GLT-1 expression in spinal cord compared with the control group (absorbance:141.38 ± 2.91 vs 106.25 ± 3.32,P =0.001).Absorbance of GLT-1 in spinal cord was significantly decreased in PTSD rats,compared with the control rats (86.11 ± 2.73 vs 106.25 ± 3.32,P =0.001).GLT-1 expression in PTSD rats treated with CTX was significantly increased compared with PTSD group (98.70 ± 3.19 vs 86.11 ± 2.73,P =0.004).VMR to CRD significantly elevated in PTSD group compared with the control group at 20,40,60 and 80 mmHg (all P ＜ 0.05,1 mmHg =0.133 kPa).VMR significantly declined in PTSD rats treated with CTX when compared with the vehicle at graded CRD pressure (all P ＜ 0.01),however,one-hour pretreatment with selective GLT-1 antagonist dihydrokainate reversed the blunted VMR to CRD produced by CTX (P =0.002).VMR significantly decreased in CTX group compared with the control group at 40,60 and 80 mmHg (all P ＜ 0.05).Conclusions The study suggests that the PTSD alters visceral sensitivity and GLT-1 overexpression mediated the analgesic effect of CTX following exposure to PTSD-like stress,identifying a specific molecular mechanism for visceral hypersensitivity which may pave the way for novel therapeutic strategies for PTSD-like conditions.