期刊文献+

祛瘀化痰二仙汤对老龄高尿酸血症大鼠阴茎海绵体NLRP3炎症小体的影响

Effect of Quyuhuatanerxian Decoction on NLRP3 Inflammatory Bodies of Penile Cavernosum in Aged Hyperuricemic Rats
下载PDF
导出
摘要 目的:探讨祛瘀化痰二仙汤对老龄高尿酸血症大鼠阴茎勃起功能保护作用的可能机制。方法:将75只18月龄雄性SD大鼠分为正常组(N组)、模型组(M组)、祛瘀化痰二仙汤高剂量组、中剂量组、低剂量组(Qh组、Qm组、Ql组),每组15只。除正常组外,其余各组大鼠均建立高尿酸血症大鼠模型,并采用阿扑吗啡(APO)实验筛选勃起功能障碍(ED)大鼠。N组和M组均给予蒸馏水[10 ml/(kg·d)],Qh组[1.296 g/(kg·d)]、Qm组[0.648 g/(kg·d)]、Ql组[0.324 g/(kg·d)],每天给予药液灌胃1次,共12周。腹腔注射麻醉,检测大鼠阴茎海绵体阴茎海绵体内压(ICP)/平均动脉压(MAP)水平;处死大鼠后酶联免疫吸附法(ELISA)检测阴茎海绵体组织匀浆中一氧化氮(NO)、内皮素-1(ET-1)、白介素-1β(IL-1β)、白介素-18(IL-18)含量,蛋白免疫印迹法检测大鼠阴茎海绵体组织匀浆中核苷酸结合寡聚化结构域样受体蛋白3(NLRP3)、凋亡相关斑点样蛋白(ASC)、半胱氨酸蛋白酶-1(Caspase-1)蛋白含量。结果:与N组比较,M组大鼠阴茎海绵体组织NO、ICP/MAP水平显著降低(P<0.05),而尿酸(UA)、NLRP3、ASC、Caspase-1、ET-1、IL-1β、IL-18水平均显著升高(P<0.05);与M组比较,Qh组阴茎海绵体组织NO、ICP/MAP水平显著升高(P<0.05),而UA、NLRP3、ASC、Caspase-1、ET-1、IL-1β、IL-18水平均显著降低(P<0.05)。结论:祛瘀化痰二仙汤可有效减轻高尿酸血液ED大鼠阴茎海绵体血管内皮功能损伤,改善勃起功能,其原因可能与其抑制阴茎海绵体组织NLRP3炎症小体介导的炎症反应有关。 Objective:To explore the possible mechanism of the protective effect of Quyuhuatanerxian decoction on erectile function in aged hyperuricemia rats.Methods:Seventy-five 18-month-old male SD rats were screened,were divided into normal group(N group),model group(M group),and Quyuhuatanerxian decoction high-dose group(Qh group),medium-dose group(Qm group),low-dose group(Ql group),with a total of 5 groups of 15 rats each.Except for the normal group,high uric acid ED model was established in all the groups.Erectile dysfunction(ED)rats were screened by apomorphine(APO)test.After successful modeling,distilled water was given in groups N group and M group[10 ml/(kg·d)];Qh group[1.296 g/(kg·d)],Qm group[0.648 g/(kg·d)],and Ql group[0.324 g/(kg·d)].The liquid was given intragastric once a day for 12 weeks.The rats were anesthetized by intraperitoneal injection,and the intracranial pressure(ICP)/mean arterial pressure(MAP)levels of the rat penis sponge were measured.The contents of nitric oxide(NO),endothelin-1(ET-1),interleukin-1β(IL-1β)and interleukin-18(IL-18)in the homogenate of cavernous tissue of the rats were determined by enzyme-linked immunosorbent assay(ELISA).The contents of nucleotide binding oligomeric domain-likereceptor protein 3(NLRP3),apoptosis-associated speck like protein(ASC)and Cysteine proteinase-1(Caspase-1)protein in the homogenate of rat cavernous tissue were determined by western blotting.Results:Compared with the N group,the expression levels of NO and ICP/MAP in penile corpus cavernosum tissues of rats in the M group were significantly decreased(P<0.05),while the expression levels of uric acid(UA),NLRP3,ASC,caspase-1,ET-1,IL-1a,IL-18,were significantly increased(P<0.05);Compared with the M group,the expression levels of NO and ICP/MAP in the corpus cavernosum of penis of Qh group were significantly increased(P<0.05),while the expression levels of UA,NLRP3,ASC,Caspase-1,ET-1,IL-1β,and IL-18 were significantly decreased(P<0.05).Conclusion:Quyuhuatanerxian decoction can effectively reduce vascular endothelial function impairment and improve erectile function in the penile corpus cavernosum of rats with hyperuricemic ED,which may be related to its inhibition of NLRP3 inflammasome mediated inflammatory response in the cavernous tissue of penis.
作者 谢红 金航 陈兰 陈智超 葛平玉 杨闽能 XIE Hong;JING Hang;CHEN Lan;CHEN Zhi-chao;GE Ping-yu;YANG Min-neng(Guizhou University of Traditional Chinese Medicine,Guiyang550025;The First Affiliated Hospital of Guizhou University of Chinese Medicine,Guiyang550001;Dejiang County National Hospital of Traditional Chinese Medicine of Guizhou Province,Dejiang565200)
出处 《实用中西医结合临床》 2023年第3期1-5,共5页 Practical Clinical Journal of Integrated Traditional Chinese and Western Medicine
基金 贵州省科学技术厅基础研究计划项目[编号:黔科合基础-ZK(2021)一般507]。
关键词 高尿酸血症 勃起功能障碍 大鼠 祛瘀化痰二仙汤 NLRP3 血管内皮功能 Hyperuricemia Erectile dysfunction Rats Quyuhuatanerxian decoction NLRP3 Vascular endothelial function
  • 相关文献

参考文献12

二级参考文献81

  • 1周素平,杨成明.炎症和心力衰竭[J].心血管病学进展,2007,28(3):493-496. 被引量:25
  • 2李红,张美玲,张兆芳,欧秀梅,周莹.大叶车前子粗多糖胶囊对小鼠急性毒性的试验[J].甘肃中医学院学报,2007,24(3):18-19. 被引量:8
  • 3Martinon F,P:trilli V, Mayor A. Gout-associated uric acid crystals activate the NALP3 inflammasome[J].Nature, 2006,440 (7081) : 237-241.
  • 4Gustafsson D, Unwin R. The pathophysiology of hyperuricae- mia and its possible relationship to cardiovascular disease,mor-bidity and mortality[J]. BMC Nephrology, 2013,14 : 164.
  • 5Zhou R, Tardivel A, Thorens B, et al. Thioredoxin-interacting protein links oxidative stress to inflammasome activation[J]. Nat Immunoh 2010,11(2) : 136-140.
  • 6Stienstra R,Joosten L A,Koenen T,et al. The inflammasome- mediated caspase-1 activation controls adipocyte differentiation and insulin sensitivity[J]. Cell Metab,2010,12(6) :593-605.
  • 7Vandanmagsar B, Youm Y H, Ravussin A, et al. The NLRP3 inflammasome instigates obesity-induced inflammation and in- sulin resistance[J].Nat Med, 2011,17(2) : 179-188.
  • 8Wen H,Gris D, Lei Y,et al. Fatty acid-induced NLRP3-ASC inflammasome activation interferes with insulin signaling[J]. Nat Irnmunol,2011,12(5) :408-415.
  • 9Stienstra R,van Diepen J A, Tack CJ,et al. Inflammasome is a cen- tral player in the induction of obesity and insulin resistance[J]. Proc Natl Acad Sci USA,2011,108(37) :15324-15329.
  • 10Mandrup Poulsen T, Pickersgill L, Donath M Y. Blockade of interleukin 1 in type 1 diabetes mellitus[J]. Nat Rev Endocri- nol,2010,6(3) :158-166.

共引文献76

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部