中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

大黄灵仙方对胆固醇结石豚鼠模型胆囊Cajal间质细胞中scf/c-kit信号通路的影响

肖丽君 甘苡榕 刘春丽 李承积 杨文 庞浇安 滕金豪 俞渊

引用本文:
Citation:

大黄灵仙方对胆固醇结石豚鼠模型胆囊Cajal间质细胞中scf/c-kit信号通路的影响

DOI: 10.3969/j.issn.1001-5256.2023.02.019
基金项目: 

广西自然科学基金项目 (2020GXNSFAA238012);

2021年“岐黄工程”高层次人才团队培育项目 (2021006);

2020年广西中医药大学第一附属医院院级博士启动基金项目 (2020BS004);

广西中医药大学2021年研究生教育创新计划项目 (YCXJ2021068)

伦理学声明:本研究方案于2021年5月25日经由广西中医药大学第一附属医院实验动物伦理委员会审批,批号:DW20191017-023,符合实验室动物管理与使用准则。
利益冲突声明:本研究不存在研究者、伦理委员会成员以及与公开研究成果有关的利益冲突。
作者贡献声明:肖丽君负责课题设计,资料分析,拟定写作思路,撰写论文;甘苡榕参与资料分析,修改论文;刘春丽、李承积、杨文、庞浇安、滕金豪负责文献检索,收集数据及数据统计分析;俞渊负责指导撰写文章并最后定稿。
详细信息
    通信作者:

    俞渊,doctoryuyuan@163.com(ORCID:0000-0001-9662-8959)

Effect of Dahuang Lingxian prescription on the scf/c-kit signaling pathway in gallbladder interstitial cells of Cajal in a guinea pig model of cholesterol gallstone

Research funding: 

Guangxi Natural Science Foundation Project (2020GXNSFAA238012);

2021 "Qihuang Project" High Level Talent Team Training Project (2021006);

2020 Hospital-level Doctoral Start-up Fund Project of the First Affiliated Hospital of Guangxi University of Traditional Chinese Medicine (2020BS004);

2021 Postgraduate Education Innovation Plan Project of Guangxi University of traditional Chinese medicine (YCXJ2021068)

More Information
  • 摘要:   目的  观察在大黄灵仙方的调控下干细胞生长因子(scf)、酪氨酸激酶受体(c-kit)的表达水平,探讨其影响胆囊动力学改变的可能机制,为大黄灵仙方预防胆石症的发生及复发提供理论依据。  方法  将45只SPF级健康雄性豚鼠随机分为正常组、模型组、中药组,其中正常组予正常饲料喂养,模型组、中药组予高脂致石饲料喂养,喂养8周后分别从各组中随机抽取5只豚鼠,肉眼观察下结石形成超过4只,则判断为模型建立成功。造模成功后中药组予大黄灵仙方灌胃,模型组予等体积生理盐水灌胃,连续灌胃给药8周后取豚鼠胆囊组织,HE染色观察观察胆囊组织的病理学改变,Western blot测定胆囊组织中TNFα的表达水平,免疫组化测定胆囊平滑肌组织中scf、c-kit的蛋白表达水平。符合正态分布的计量资料多组间比较采用单因素方差分析,进一步两两比较采用LSD多重比较法。  结果  HE染色显示模型组胆囊组织炎症明显,中药组胆囊组织内炎症程度较模型组明显减轻。Western blot结果表明在模型组中,胆囊组织中TNFα的表达水平最高,中药组次之,正常组最低(P值均<0.05);免疫组化结果表明豚鼠胆囊平滑肌组织中scf、c-kit蛋白在正常组、中药组中的表达水平显著高于模型组(P值均<0.05)。  结论  大黄灵仙方能增强胆囊动力功能,其作用机制可能与上调胆囊Cajal间质细胞中的scf、c-kit信号通路有关。

     

  • 图  1  豚鼠体质量的变化情况

    Figure  1.  Changes in body mass of guinea pigs

    图  2  各组豚鼠胆囊组织的病理情况(HE染色,×200)

    注:a,正常组;b,模型组;c,中药组。

    Figure  2.  Pathological changes of gallbladder tissues of guinea pigs in each group (HE staining, ×200)

    图  3  大黄灵仙方干预下TNFα的表达情况

    Figure  3.  Expression of TNFα under the intervention of Dahuang lingxian formula

    图  4  大黄灵仙方对TNFα表达水平的影响

    Figure  4.  Effect of Dahuang lingxian formula on TNFα expression

    图  5  大黄灵仙方干预下TNF、scf、c-kit的表达情况(免疫组化,×100)

    Figure  5.  Expression of TNFα, scf and c-kit under the intervention of Dahuang lingxian formula (immunohisto-chemistry, ×100)

    表  1  大黄灵仙方对TNFα、scf、c-kit表达水平的影响

    Table  1.   Effect of Dahuang Lingxian formula on the expression of TNFα, scf and c-kit

    组别 TNFα c-kit SCF
    正常组 3.48±1.791)2) 29.35±8.971)2) 28.11±5.631)2)
    模型组 26.42±3.87 13.32±2.01 15.46±3.14
    中药组 17.35±2.751) 21.11±2.721) 23.08±6.411)
    F 108.91 14.70 10.28
    P <0.05 <0.05 <0.05
    注:与模型组比较,1)P<0.05;与中药组比较,2)P<0.05。
    下载: 导出CSV
  • [1] STINTON LM, SHAFFER EA. Epidemiology of gallbladder disease: cholelithiasis and cancer[J]. Gut Liver, 2012, 6(2): 172-187. DOI: 10.5009/gnl.2012.6.2.172.
    [2] SHABANZADEH DM. Incidence of gallstone disease and complications[J]. Curr Opin Gastroenterol, 2018, 34(2): 81-89. DOI: 10.1097/MOG.0000000000000418.
    [3] LAMBERTS MP. Indications of cholecystectomy in gallstone disease[J]. Curr Opin Gastroenterol, 2018, 34(2): 97-102. DOI: 10.1097/MOG.0000000000000419.
    [4] PENG YY, TAN YY. Analysis of the role of Cajal interstitial cells in the formation of gallstones[J]. Labeled Immunoassays Clin Med, 2016, 23(7): 817-819. DOI: 10.11748/bjmy.issn.1006-1703.2016.07.028.

    彭雅亚, 谭宇彦. Cajal间质细胞在胆囊结石形成中的作用分析[J]. 标记免疫分析与临床, 2016, 23(7): 817-819. DOI: 10.11748/bjmy.issn.1006-1703.2016.07.028.
    [5] ZHAO JN, FAN Y, WU SD. Advances in the relationship between Cajal-like interstitial cells of the gallbladder and cholesterol stone formation in the gallbladder[J]. Med Recapitulate, 2019, 25(21): 4180-4184, 4190. DOI: 10.3969/j.issn.1006-2084.2019.21.004.

    赵健楠, 范莹, 吴硕东. 胆囊Cajal样间质细胞与胆囊胆固醇结石形成关系的研究进展[J]. 医学综述, 2019, 25(21): 4180-4184, 4190. DOI: 10.3969/j.issn.1006-2084.2019.21.004.
    [6] XU JH, FAN Y. Effect of cholesterol on Cajal-like interstitial cells of guinea pig gallbladder isolated and cultured in vitro[J]. Chin J Clin Res, 2019, 32(11): 1457-1461. DOI: 10.13429/j.cnki.cjcr.2019.11.001.

    许金煌, 范莹. 胆固醇对体外分离培养的豚鼠胆囊Cajal样间质细胞的影响[J]. 中国临床研究, 2019, 32(11): 1457-1461. DOI: 10.13429/j.cnki.cjcr.2019.11.001.
    [7] YU Y, YIN X, TANG QL, et al. Study on the regulation of NF-κB signaling pathway-related factor genes by Dahuang Lingxian formula to affect the inflammatory response of bile duct cells[J]. Lishizhen Med Mater Med Res, 2020, 31(5): 1034-1037. DOI: 10.3969/j.issn.1008-0805.2020.05.003.

    俞渊, 尹星, 唐乾利, 等. 大黄灵仙方调控NF-κB信号通路相关因子基因影响胆管细胞炎性反应的研究[J]. 时珍国医国药, 2020, 3(5): 1034-1037. DOI: 10.3969/j.issn.1008-0805.2020.05.003.
    [8] WANG QJ, TANG QL, YU Y, et al. Dahuang Lingxian formula capsule regulates TGF-β1 mRNA and Smad2 in bile duct endothelial cells[J]. Lishizhen Med Mater Med Res, 2014, 25(12): 2833-2835. DOI: 10.3969/j.issn.1008-0805.2014.12.006.

    王清坚, 唐乾利, 俞渊, 等. 大黄灵仙胶囊调节胆管内皮细胞TGF-β1mRNA、Smad2/3mRNA表达的实验研究[J]. 时珍国医国药, 2014, 25(12): 2833-2835. DOI: 10.3969/j.issn.1008-0805.2014.12.006.
    [9] FENG H, WANG F, WANG C. C-Kit expression in the gallbladder of guinea pig with chronic calculous cholecystitis and the effect of Artemisia capillaris Thunb on interstitial cells of Cajal[J]. Iran J Basic Med Sci, 2016, 19(7): 720-725.
    [10] CHEN Q. Experimental methodology of Chinese pharmacology[M]. Beijing: People's Health Publishing House, 1994: 215.

    陈奇. 中药药理学实验方法学[M]. 北京: 人民卫生出版社, 1994: 215.
    [11] ANSTÖTZ M, LEE SK, NEBLETT TI, et al. Experience-dependent regulation of Cajal-retzius cell networks in the developing and adult mouse hippocampus[J]. Cereb Cortex, 2018, 28(2): 672-687. DOI: 10.1093/cercor/bhx153.
    [12] ORTIZ-HIDALGO C, de LEON BOJORGE B, ALBORES-SAAVEDRA J. Stromal tumor of the gallbladder with phenotype of interstitial cells of Cajal: a previously unrecognized neoplasm[J]. Am J Surg Pathol, 2000, 24(10): 1420-1423. DOI: 10.1097/00000478-200010000-00013.
    [13] LAVOIE B, BALEMBA OB, NELSON MT, et al. Morphological and physiological evidence for interstitial cell of Cajal-like cells in the guinea pig gallbladder[J]. J Physiol, 2007, 579(Pt 2): 487-501. DOI: 10.1113/jphysiol.2006.122861.
    [14] PASTERNAK A, GAJDA M, GIL K, et al. Evidence of interstitial Cajal-like cells in human gallbladder[J]. Folia Histochem Cytobiol, 2012, 50(4): 581-585. DOI: 10.5603/19673.
    [15] CHEN L, YU B. Telocytes and interstitial cells of Cajal in the biliary system[J]. J Cell Mol Med, 2018, 22(7): 3323-3329. DOI: 10.1111/jcmm.13643.
    [16] FAUSSONE-PELLEGRINI MS, VANNUCCHI MG, LEDDER O, et al. Plasticity of interstitial cells of Cajal: a study of mouse colon[J]. Cell Tissue Res, 2006, 325(2): 211-217. DOI: 10.1007/s00441-006-0174-8.
    [17] MEI F, HAN J, HUANG Y, et al. Plasticity of interstitial cells of cajal: a study in the small intestine of adult Guinea pigs[J]. Anat Rec (Hoboken), 2009, 292(7): 985-993. DOI: 10.1002/ar.20928.
    [18] TORIHASHI S, NISHI K, TOKUTOMI Y, et al. Blockade of kit signaling induces transdifferentiation of interstitial cells of cajal to a smooth muscle phenotype[J]. Gastroenterology, 1999, 117(1): 140-148. DOI: 10.1016/s0016-5085(99)70560-3.
    [19] MEI F, ZHU J, GUO S, et al. An age-dependent proliferation is involved in the postnatal development of interstitial cells of Cajal in the small intestine of mice[J]. Histochem Cell Biol, 2009, 131(1): 43-53. DOI: 10.1007/s00418-008-0515-7.
    [20] HUIZINGA JD, THUNEBERG L, KLVPPEL M, et al. W/kit gene required for interstitial cells of Cajal and for intestinal pacemaker activity[J]. Nature, 1995, 373(6512): 347-349. DOI: 10.1038/373347a0.
    [21] ISOZAKI K, HIROTA S, NAKAMA A, et al. Disturbed intestinal movement, bile reflux to the stomach, and deficiency of c-kit-expressing cells in Ws/Ws mutant rats[J]. Gastroenterology, 1995, 109(2): 456-464. DOI: 10.1016/0016-5085(95)90333-x.
    [22] ISOZAKI K, HIROTA S. Gain-of-function mutations of receptor tyrosine kinases in gastrointestinal stromal tumors[J]. Curr Genomics, 2006, 7(8): 469-475. DOI: 10.2174/138920206779315755.
    [23] MA WW, LI CQ, YU HL, et al. The oxysterol 27-hydroxycholesterol increases oxidative stress and regulate Nrf2 signaling pathway in astrocyte cells[J]. Neurochem Res, 2015, 40(4): 758-766. DOI: 10.1007/s11064-015-1524-2.
    [24] CHUA NK, COATES HW, BROWN AJ. Cholesterol, cancer, and rebooting a treatment for athlete's foot[J]. Sci Transl Med, 2018, 10(437): eaat3741. DOI: 10.1126/scitranslmed.aat3741.
    [25] WAN JF, CHU SF, ZHOU X, et al. Ursodeoxycholic acid protects interstitial Cajal-like cells in the gallbladder from undergoing apoptosis by inhibiting TNF-α expression[J]. Acta Pharmacol Sin, 2018, 39(9): 1493-1500. DOI: 10.1038/aps.2017.206.
  • 加载中
图(5) / 表(1)
计量
  • 文章访问数:  694
  • HTML全文浏览量:  396
  • PDF下载量:  93
  • 被引次数: 0
出版历程
  • 收稿日期:  2022-07-13
  • 录用日期:  2022-08-18
  • 出版日期:  2023-02-20
  • 分享
  • 用微信扫码二维码

    分享至好友和朋友圈

目录

    /

    返回文章
    返回