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纸质出版日期:2017
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耿利华, 谈勇. 坤泰胶囊对卵巢储备功能下降大鼠卵巢凋亡调控蛋白Bcl-2,Bax表达的影响[J]. 中国实验方剂学杂志, 2017,23(8):138-143.
GENG Li-hua, TAN Yong. Effect of Kuntai Capsule on Expressions of Bcl-2 and Bax Protein in Rats Ovaries with Decreasing Ovarian Reserve[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(8): 138-143.
耿利华, 谈勇. 坤泰胶囊对卵巢储备功能下降大鼠卵巢凋亡调控蛋白Bcl-2,Bax表达的影响[J]. 中国实验方剂学杂志, 2017,23(8):138-143. DOI: 10.13422/j.cnki.syfjx.2017080138.
GENG Li-hua, TAN Yong. Effect of Kuntai Capsule on Expressions of Bcl-2 and Bax Protein in Rats Ovaries with Decreasing Ovarian Reserve[J]. Chinese journal of experimental traditional medical formulae, 2017, 23(8): 138-143. DOI: 10.13422/j.cnki.syfjx.2017080138.
目的:探讨坤泰胶囊对去氧乙烯基环己烯(4-vinylcyclohexene diepoxide,VCD)所致卵巢储备功能下降(decreasing ovarian reserve,DOR)大鼠凋亡调控蛋白B细胞淋巴瘤/白血病-2原癌基因(Bcl-2),Bcl-2相关X蛋白(Bax)表达的影响,研究该药的作用机制。方法: SD雌性大鼠连续腹腔注射VCD(80 mg·kg-1)15 d,建立与人类相似的生理性卵巢储备功能下降模型。将动物分为正常组,模型组,坤泰胶囊高、中、低剂量组(1.89,0.63,0.21 g·kg-1),补佳乐(戊酸雌二醇,0.13 mg·kg-1)组,于造模第1天开始灌胃给药,每天1次,连续45 d。酶联免疫吸附测定(ELISA)法检测大鼠血清激素卵泡刺激素(FSH),黄体生成素(LH)及雌二醇(E2)水平,苏木素-伊红(HE)染色观察卵巢、子宫的病理组织变化,蛋白质免疫印迹(Western blot)法检测卵巢组织Bcl-2,Bax蛋白的表达。结果:与正常组比较,模型组FSH与LH明显升高,E2明显降低(P<0.05);模型组卵巢、子宫体积明显缩小,原始卵泡与初级卵泡数目明显减少,子宫内膜变薄,腺体数目减少;模型组大鼠卵巢Bcl-2蛋白表达明显减少,Bax蛋白表达明显增加(P<0.05),Bcl-2/Bax显著下降(P<0.01)。与模型组比较,坤泰胶囊高、中、低剂量组FSH明显降低,E2明显升高(P<0.05);补佳乐组FSH,LH明显降低,E2明显升高(P<0.05)。各给药组卵巢、子宫体积增大,原始卵泡与初级卵泡数目增多,子宫内膜变厚,腺体数目增加,改善程度顺序依次为坤泰胶囊低、中、高剂量组、补佳乐组。坤泰胶囊高、中、低剂剂量组及补佳乐组大鼠卵巢Bcl-2蛋白表达明显增加(P < 0.05,P < 0.01);坤泰胶囊高、中、低剂量组及补佳乐药组大鼠卵巢Bax蛋白表达减少(P<0.05);坤泰胶囊高、中、低剂量组及补佳乐组大鼠卵巢Bcl-2/Bax升高(P < 0.05,P < 0.01)。结论:坤泰胶囊可能通过上调卵巢Bcl-2蛋白表达及下调Bax蛋白表达,抑制卵泡的凋亡,从而改善卵巢功能。
Objective: To study the effect of Kuntai capsule on expressions of B-cell lymphoma/leukemia 2 (Bcl-2) and Bcl-2 associated X protein (Bax) protein in rats with decreasing ovaries reserve (DOR) induced by 4-vinylcyclohexene diepoxide (VCD). Method: The model of DOR of Sprague-Dawley female rats was established through intraperitoneal injection with 80 mg·kg-1 of VCD for continuously 15 days. Since the 1st day of modeling
the SD rats were orally administered with drugs for 45 days. They were divided into the normal group
the model control group
high
middle and low-dose Kuntai capsule groups (1.89
0.63
0.21 g·kg-1)
and Estradio Valerate group (0.13 mg·kg-1). follicle-stimulating (FSH)
lactogenic hormone (LH)
estradiol (E2) were detected by ELISA method. HE staining was used to observed histopathologic changes in ovary and uterus. Expression levels of Bcl-2 and Bax protein in rats ovarian were detected by Western blot method. Result: Compared to the normal group
FSH
LH of the model control group increased strikingly
and E2 decreased (P<0.05). Ovarian and uterus were shrunk remarkably. The numbers of primordial follicles and primary follicles reduced obviously. The endometrium became thin. The expression of Bcl-2 protein of model group decreased obviously
whereas the expression of Bax protein of model group increased (P<0.05)
Bcl-2/Bax ratio of model group decreased sharply (P<0.01). Compared with the model group
FSH of high
middle and low-dose Kuntai capsule group decreased
while E2 increased (P<0.05). FSH
LH of Estradio Valerate group decreased
while E2 increased(P<0.05). After intragastric administration
the volume of ovaries and uteruses of Kuntai capsule group and Estradio Valerate group increased
and the numbers of primordial follicles and primary follicles increased. The endometrium became thick. The order of alleviation degree from low to high was low
middle and high-dose Kuntai capsule groups and Estradio Valerate group. The expression of Bcl-2 protein of high
middle and low-dose Kuntai capsule groups and Estradio Valerate group significantly increased (P < 0.05
P < 0.01); The expression of Bax protein of high
middle and low-dose Kuntai capsule groups and Estradio Valerate group significantly decreased (P<0.05). Bcl-2/Bax ratio of high
middle and low-dose Kuntai capsule groups and Estradio Valerate group increased (P < 0.05
P < 0.01). Conclusion: Kuntai capsule can improve the function of ovaries by up-regulating the expression of Bcl-2 protein and down-regulating the expression of Bax protein in ovarian.
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