天津医药
天津醫藥
천진의약
TIANJIN MEDICAL JOURNAL
2013年
8期
796-798
,共3页
李战永%孔德强%杨卓%张涛
李戰永%孔德彊%楊卓%張濤
리전영%공덕강%양탁%장도
硫化氢%神经胶质瘤%新生血管化,病理性%基质金属蛋白酶2%抗原,CD34%免疫组织化学%大鼠, Sprague-Dawley
硫化氫%神經膠質瘤%新生血管化,病理性%基質金屬蛋白酶2%抗原,CD34%免疫組織化學%大鼠, Sprague-Dawley
류화경%신경효질류%신생혈관화,병이성%기질금속단백매2%항원,CD34%면역조직화학%대서, Sprague-Dawley
hydrogen sulfide%glioma%neovascularization,pathologic%matrix metalloproteinase 2%antigens,CD34%im-munohistochemistry%rats,Sprague-Dawley
目的探讨外源性硫化氢(H2S)对大鼠恶性胶质瘤内血管新生的影响。方法成年雄性SD大鼠20只,随机分成肿瘤组和肿瘤-H2S组,每组10只。2组大鼠均脑内注射C6细胞,1周后,肿瘤组腹腔注射生理盐水,肿瘤-H2S组腹腔注射外源性H2S,即硫氢化钠(NaHS)溶液。均正常饲养,3周后断头取脑。组织病理学观察瘤体结构以及瘤内微血管生成情况,免疫组化评估瘤体内CD34及基质金属蛋白酶(MMP)-2的表达情况;并计数瘤内微血管密度(MVD)。结果肿瘤组与肿瘤-H2S组大鼠脑内均可见明显的肿瘤组织;与对侧正常脑组织相比,瘤内毛细血管明显增多;肿瘤-H2S组瘤体内有更多的CD34和MMP-2表达,肿瘤-H2S组瘤内MVD明显高于肿瘤组(均P<0.01)。结论外源性H2S能促进大鼠恶性胶质瘤内的血管新生,其机制可能与H2S促进瘤体内MMP-2的表达有关。
目的探討外源性硫化氫(H2S)對大鼠噁性膠質瘤內血管新生的影響。方法成年雄性SD大鼠20隻,隨機分成腫瘤組和腫瘤-H2S組,每組10隻。2組大鼠均腦內註射C6細胞,1週後,腫瘤組腹腔註射生理鹽水,腫瘤-H2S組腹腔註射外源性H2S,即硫氫化鈉(NaHS)溶液。均正常飼養,3週後斷頭取腦。組織病理學觀察瘤體結構以及瘤內微血管生成情況,免疫組化評估瘤體內CD34及基質金屬蛋白酶(MMP)-2的錶達情況;併計數瘤內微血管密度(MVD)。結果腫瘤組與腫瘤-H2S組大鼠腦內均可見明顯的腫瘤組織;與對側正常腦組織相比,瘤內毛細血管明顯增多;腫瘤-H2S組瘤體內有更多的CD34和MMP-2錶達,腫瘤-H2S組瘤內MVD明顯高于腫瘤組(均P<0.01)。結論外源性H2S能促進大鼠噁性膠質瘤內的血管新生,其機製可能與H2S促進瘤體內MMP-2的錶達有關。
목적탐토외원성류화경(H2S)대대서악성효질류내혈관신생적영향。방법성년웅성SD대서20지,수궤분성종류조화종류-H2S조,매조10지。2조대서균뇌내주사C6세포,1주후,종류조복강주사생리염수,종류-H2S조복강주사외원성H2S,즉류경화납(NaHS)용액。균정상사양,3주후단두취뇌。조직병이학관찰류체결구이급류내미혈관생성정황,면역조화평고류체내CD34급기질금속단백매(MMP)-2적표체정황;병계수류내미혈관밀도(MVD)。결과종류조여종류-H2S조대서뇌내균가견명현적종류조직;여대측정상뇌조직상비,류내모세혈관명현증다;종류-H2S조류체내유경다적CD34화MMP-2표체,종류-H2S조류내MVD명현고우종류조(균P<0.01)。결론외원성H2S능촉진대서악성효질류내적혈관신생,기궤제가능여H2S촉진류체내MMP-2적표체유관。
Objective To investigate the stimulating effect of exogenous hydrogen sulfide (H2S) on angiogenesis in glioblastoma (GBM). Methods Twenty adult Sprague-Dawley (SD) rats were randomly divided into two groups, glioma group (C6 glioma cell intracerebral implantation, n=10) and glioma-H2S group (C6 glioma cell intracerebral implantation and sodium hydrosulfide (NaHS) intraperitoneal injection, n=10). The tumor-bearing rat model was established by intracerebral injection of rat C6 glioma cells. After one week, normal saline was injected in glioma group and NaHS was injected in glio-ma-H2S group. Food and water were freely available during all phases of the experiment. After three weeks, rats were decapi-tated and brains were removed. HE staining was performed to show tumor structure and intratumoral angiogenesis. The immu-nohistochemical analysis was used to detect the expressions of CD34 and MMP-2, respectively. The microvessel density (MVD) in GBM was also measured. Results HE staining showed that the implanted tumors were predominantly spheroid with clear border and no capsule could be detected. The neovascular proliferations were observed in tumors. There were high-er expressions of CD34 and MMP-2 in glioma-H2S group. The value of MVD was significantly higher in glioma-H2S group than that of glioma group (P<0.01). Conclusion Exogenous H2S serves as a stimulator of angiogenesis in the development of rat GBM, which may be related with the increased MMP-2 expression promoted by H2S.