解剖学报
解剖學報
해부학보
ACTA ANATOMICA SINICA
2010年
2期
276-280
,共5页
常青%钱晓菁%许增禄%张成侠
常青%錢曉菁%許增祿%張成俠
상청%전효정%허증록%장성협
棉酚%甾体激素%精母细胞%吞噬%体视学%大鼠
棉酚%甾體激素%精母細胞%吞噬%體視學%大鼠
면분%치체격소%정모세포%탄서%체시학%대서
Gossypol%Steroid hormone%Spermatocyte%Phagocytosis%Stereology%Rat
目的 探讨低剂量棉酚和甾体激素联合用药对睾丸精母细胞数量、凋亡和支持细胞吞噬作用的影响.方法 本实验采用大鼠喂服棉酚与甾体激素联合用药方式[棉酚12.5mg/(kg·d)+去氧孕烯125μg/(kg·d)+炔雌醇25μg/(kg·d)+十一酸睾丸酮100mg/(kg·d)],与单独喂服相同剂量的棉酚或激素的大鼠及喂服载体溶剂的大鼠相对照,用药4、6和8周取睾丸组织,应用体视学、原位缺口末端标记(TUNEL)和油红O染色的方法 ,观察精母细胞和球形精子细胞数量、凋亡和支持细胞吞噬作用. 结果 联合用药中,甾体激素成分可明显减少精母细胞和球形精子细胞的数量,精母细胞凋亡增加并同时伴有生精上皮油红O染色的增强. 结论 精母细胞凋亡并被支持细胞吞噬是联合用药抗生育机制之一.
目的 探討低劑量棉酚和甾體激素聯閤用藥對睪汍精母細胞數量、凋亡和支持細胞吞噬作用的影響.方法 本實驗採用大鼠餵服棉酚與甾體激素聯閤用藥方式[棉酚12.5mg/(kg·d)+去氧孕烯125μg/(kg·d)+炔雌醇25μg/(kg·d)+十一痠睪汍酮100mg/(kg·d)],與單獨餵服相同劑量的棉酚或激素的大鼠及餵服載體溶劑的大鼠相對照,用藥4、6和8週取睪汍組織,應用體視學、原位缺口末耑標記(TUNEL)和油紅O染色的方法 ,觀察精母細胞和毬形精子細胞數量、凋亡和支持細胞吞噬作用. 結果 聯閤用藥中,甾體激素成分可明顯減少精母細胞和毬形精子細胞的數量,精母細胞凋亡增加併同時伴有生精上皮油紅O染色的增彊. 結論 精母細胞凋亡併被支持細胞吞噬是聯閤用藥抗生育機製之一.
목적 탐토저제량면분화치체격소연합용약대고환정모세포수량、조망화지지세포탄서작용적영향.방법 본실험채용대서위복면분여치체격소연합용약방식[면분12.5mg/(kg·d)+거양잉희125μg/(kg·d)+결자순25μg/(kg·d)+십일산고환동100mg/(kg·d)],여단독위복상동제량적면분혹격소적대서급위복재체용제적대서상대조,용약4、6화8주취고환조직,응용체시학、원위결구말단표기(TUNEL)화유홍O염색적방법 ,관찰정모세포화구형정자세포수량、조망화지지세포탄서작용. 결과 연합용약중,치체격소성분가명현감소정모세포화구형정자세포적수량,정모세포조망증가병동시반유생정상피유홍O염색적증강. 결론 정모세포조망병피지지세포탄서시연합용약항생육궤제지일.
Objective To investigate effects of combined regimen of low dose gossypol with steroid hormones on apoptosis of spermatocyte and phagocytosis of sertoli cells. Methods Adult male rats were divided into four groups randomly, group GH: rats were fed orally with gossypol(GA) [ 12.5mg / (kg·d) ] and desogestrel(DSG)[125μg/(kg·d) ]/ethinyloestradil(E)[25μg/ (kg·d) ]/testosterone undecanoate(TU)[100mg/(kg·d) ]; group G: a single does of GA[12.5mg/(kg·d ) ] was given; group H: DSG[125μg/(kg·d) ]/E[25μg/(kg·d) ]/TU[100mg/(kg·d) ] were administered; group C: rats only received vehicle(1% methyl cellulose). Testes from all the rats were removed at 4, 6 and 8 weeks after treatment for counting of spermatocyte and round spermatid using stereological assay, and for detecting apoptosis of spermatocyte and phagocytosis of sertoli cell by TUNEL and oil red O staining respectively. Results In GH group, the number of spermatocyte and round spermatid were reduced, while apoptosis of spermatocyte and staining of oil red O in seminiferous epithelium increased significantly. All changes were caused by steroid hormones in the combined regimen. Conclusion Induction of apoptosis of spermatocyte and then being phagocytosed by Sertoli cell is one of antifertility mechanisms of the combined regimen.