Ginkgo biloba extract 761 reduces vascular permeability of the ovary and improves the symptom of ovarian hyperstimulation syndrome in a rat model

被引:9
作者
Zhang, Jie [1 ]
Huang, Jie [2 ]
He, Xinhuan [1 ]
Li, Ning [1 ]
Miao, Yu [3 ]
Li, Beiqing [1 ]
Shao, Xiaoguang [1 ]
Wang, Ningning [4 ]
机构
[1] Dalian Municipal Women & Childrens Med Ctr, Reprod & Genet Ctr, Dalian, Liaoning, Peoples R China
[2] Dalian Municipal Women & Childrens Med Ctr, Lab Dept, Dalian, Liaoning, Peoples R China
[3] Dalian Municipal Women & Childrens Med Ctr, Tradit Chinese Med Dept, Dalian, Liaoning, Peoples R China
[4] Dalian Med Univ, Sch Publ Hlth, Dept Food Nutr & Safety, 9 Lvshun South Rd, Dalian 116044, Liaoning, Peoples R China
关键词
Ginkgo biloba extract; EGb761; ovarian hyperstimulation syndrome; OHSS; vascular permeability; VEGF; VEGFR; ENDOTHELIAL GROWTH-FACTOR; PATHOPHYSIOLOGY;
D O I
10.1080/09513590.2022.2034147
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Ginkgo biloba extract (EGb) has been widely applied in the treatment of cerebrovascular and neurological diseases. However, the effect of EGb761 on ovarian hyperstimulation syndrome (OHSS), a vascular disorder and life-threatening complication of In Vitro Fertilization and Intracytoplasmic Sperm Injection therapy (IVF/ICSI), has not been evaluated. Materials and methods Forty female Wistar rats aged 22-days old (D22) were divided into eight groups: Control rats received intraperitoneal injection of saline for 5 consecutive days (D22-D26); OHSS model group received 10 IU equine chorionic gonadotropin (eCG) for 4 consecutive days (D22-D25) and 30 IU of human chorionic gonadotropin (hCG) on the 5th day (D26); Prophylactic treatment group received three doses of EGb761 (50, 100, and 200 mg/kg/d) one hour before injection of eCG (hCG) for 7 consecutive days; Therapeutic treatment group received three doses of EGb761 (50, 100, and 200 mg/kg/d) 48 h after injection of eCG (hCG) for 7 consecutive days. Results All three doses of EGb761 therapeutic medication significantly reduced ovarian mass index in the OHSS model (p <= .01). Further, the therapeutic treatment group exhibited improved vascular permeability, decreased estradiol and progesterone levels, lower corpus luteum, and higher follicle numbers compared with the OHSS model. Elevated protein expression of vascular endothelial growth factor (VEGF) and VEGF receptor (VEGFR) in both ovary and kidney of the OHSS model was restrained by EGb761 therapeutic treatment. Conclusions EGb761 therapeutic medication decreases vascular permeability in OHSS rat model by inhibiting VEGF and VEGFR expression, which may contribute to the treatment of OHSS.
引用
收藏
页码:318 / 323
页数:6
相关论文
共 18 条
[1]   What is the impact of short- and long-term supplementation of either cabergoline or clarithromycin on resolving rat ovarian hyperstimulation syndrome (OHSS) model? [J].
Atilgan, Remzi ;
Pala, Sehmus ;
Yavuzkir, Seyda ;
Baspinar, Melike ;
Yilmaz, Mustafa ;
Ilhan, Nevin .
JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2019, 39 (05) :687-694
[2]   Ovarian hyperstimulation: past, present, and future [J].
Feinberg, Eve C. .
FERTILITY AND STERILITY, 2016, 106 (06) :1330-1330
[3]   Administration of moderate and high doses of gonadotropins to female rats increases ovarian vascular endothelial growth factor (VEGF) and VEGF receptor-2 expression that is associated to vascular hyperpermeability [J].
Gömez, R ;
Simón, C ;
Remohí, J ;
Pellicer, A .
BIOLOGY OF REPRODUCTION, 2003, 68 (06) :2164-2171
[4]   Vascular endothelial growth factor receptor-2 activation induces vascular permeability in hyperstimulated rats, and this effect is prevented by receptor blockade [J].
Gómez, R ;
Simón, C ;
Remohí, J ;
Pellicer, A .
ENDOCRINOLOGY, 2002, 143 (11) :4339-4348
[5]   The pathophysiology of ovarian hyperstimulation syndrome: an unrecognized compartment syndrome [J].
Grossman, Lisa C. ;
Michalakis, Konstantinos G. ;
Browne, Hyacinth ;
Payson, Mark D. ;
Segars, James H. .
FERTILITY AND STERILITY, 2010, 94 (04) :1392-1398
[6]   The VEGF and PEDF levels in the follicular fluid of patients co-treated with LETROZOLE and gonadotropins during the stimulation cycle [J].
Haas, Jigal ;
Bassil, Rawad ;
Gonen, Noa ;
Meriano, Jim ;
Jurisicova, Andrea ;
Casper, Robert F. .
REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, 2018, 16
[7]   Resistance to Anti-Angiogenic Therapy in Cancer-Alterations to Anti-VEGF Pathway [J].
Itatani, Yoshiro ;
Kawada, Kenji ;
Yamamoto, Takamasa ;
Sakai, Yoshiharu .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (04)
[8]   Melatonin stimulates VEGF expression in human granulosa-lutein cells: A potential mechanism for the pathogenesis of ovarian hyperstimulation syndrome [J].
Li, Yiran ;
Fang, Lanlan ;
Zhang, Ruizhe ;
Wang, Sijia ;
Li, Yuxi ;
Yan, Yang ;
Yu, Yiping ;
Cheng, Jung-Chien ;
Sun, Ying-Pu .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2020, 518
[9]   Ovarian hyperstimulation syndrome: pathophysiology, staging, prediction and prevention [J].
Nastri, C. O. ;
Teixeira, D. M. ;
Moroni, R. M. ;
Leitao, V. M. S. ;
Martins, W. P. .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2015, 45 (04) :377-393
[10]   Polymorphisms of VEGF and VEGF receptors are associated with the occurrence of ovarian hyperstimulation syndrome (OHSS)-a retrospective case-control study [J].
Nouri, Kazem ;
Haslinger, Peter ;
Szabo, Ladislaus ;
Sator, Michael ;
Schreiber, Martin ;
Schneeberger, Christian ;
Pietrowski, Detlef .
JOURNAL OF OVARIAN RESEARCH, 2014, 7