Jian-Pi-Yi-Shen decoction inhibits mitochondria-dependent granulosa cell apoptosis in a rat model of POF

被引:0
|
作者
Jiang, Xiao-Lin [1 ,2 ]
Tai, He [3 ,4 ]
Kuang, Jin-Song [5 ]
Zhang, Jing-Yi [6 ]
Cui, Shi-Chao [7 ]
Lu, Yu-Xuan [8 ]
Qi, Shu-Bo [2 ]
Zhang, Shi-Yu [2 ]
Li, Shun -Min [1 ]
Chen, Jian-Ping [4 ]
Meng, Xian-Sheng [3 ]
机构
[1] Guangzhou Univ Tradit Chinese Med, Affiliated Hosp 4, Shenzhen Tradit Chinese Med Hosp, Dept Nephrol, Shenzhen, Peoples R China
[2] Liaoning Univ Tradit Chinese Med, Key Lab Minist Educ Tradit Chinese Med Viscera Sta, Shenyang, Peoples R China
[3] Liaoning Univ Tradit Chinese Med, Coll Pharm, Dalian, Peoples R China
[4] Chinese Peoples Armed Police Forces, Dept Internal Med, Liaoning Prov Corps Hosp, Shenyang, Peoples R China
[5] Fourth Peoples Hosp Shenyang, Dept Endocrinol & Metab, Shenyang, Peoples R China
[6] Gen Hosp Northern Theater Command, Dept Pharm, Shenyang, Peoples R China
[7] Guangdong Prov Fertil Hosp, Guangdong Prov Reprod Sci Inst, NHC Key Lab Male Reprod & Genet, Guangzhou, Peoples R China
[8] Chinese Capital Med Univ, Coll Basic Med Sci, Beijing, Peoples R China
来源
AGING-US | 2022年 / 14卷 / 20期
基金
中国国家自然科学基金;
关键词
Jian-Pi-Yi-Shen; premature ovarian failure; mitochondrial dysfunction; granulosa cell; apoptosis; PREMATURE OVARIAN FAILURE; ENDOPLASMIC-RETICULUM; EXPRESSION; DYNAMICS; SURVIVAL; FISSION; ATRESIA; GENES; DEATH; BCL-2;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As a widely applied traditional Chinese medicine (TCM), Jian-Pi-Yi-Shen (JPYS) decoction maybe applied in curing premature ovarian failure (POF) besides chronic kidney disease (CKD). In vivo experiments, 40 female SD (8-week-old) rats were randomized into four groups, namely, control group (negative control), POF model group, JPYS treatment group, and triptorelin treatment group (positive control). JPYS group was treated with JPYS decoction (oral, 11 g/kg) for 60 days, and the triptorelin group was treated with triptorelin (injection, 1.5 mg/kg) for 10 days before the administration of cyclophosphamide (CTX) (50 mg/kg body weight) to establish POF model. We examined apoptosis, mitochondrial function, and target gene (ASK1/JNK pathway and mitochondrial fusion/fission) expression. In vitro experiments, the KGN human granulosa cell line was used. Cells were pretreated with CTX (20, 40, and 60 mu g/mL) for 24 h, followed by JPYS-containing serum (2, 4, and 8 %) for 24 h. Thereafter, these cells were employed to assess apoptosis, mitochondrial function, and target gene levels of protein and mRNA. In vivo, JPYS alleviated injury and suppressed apoptosis in POF rats. In addition, JPYS improved ovarian function. JPYS inhibit apoptosis of granulosa cells through improving mitochondrial function by activating ASK1/JNK pathway. In vitro, JPYS inhibited KGN cell apoptosis through inhibited ASK1/JNK pathway and improved mitochondrial function. The effects of GS-49977 were similar to those of JPYS. During POF, mitochondrial dysfunction occurs in the ovary and leads to granulosa cell apoptosis. JPYS decoction improves mitochondrial function and alleviates apoptosis through ASK1/JNK pathway.
引用
收藏
页码:8321 / 8345
页数:25
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