Bishop C V, Lee D M, Slayden O D, Li X
Division of Reproductive & Developmental Sciences, Oregon National Primate Research Center, Beaverton, OR, 97006, USA.
Obstetrics & Gynecology, Oregon Health & Science University, Portland, OR, 97239, USA.
J Ovarian Res. 2017 Jul 6;10(1):41. doi: 10.1186/s13048-017-0340-5.
Ovarian hyperstimulation syndrome (OHSS) is a disorder associated with elevated serum VEGFA following chorionic gonadotropin (hCG) exposure in controlled ovarian stimulation (COS) cycles in women. In this study, we tested the effect of intravenous VEGFA neutralization on OHSS-like symptoms and vascular function in rhesus macaques during COS cycles.
Monkeys (n = 8) were treated with 3 COS protocols and assigned randomly to groups as follows: 1) COS alone (Control, n = 5); 2) COS + VEGF mAb Avastin 19 ± 5 h before hCG (Avastin pre-hCG; n = 6); 3) COS + Avastin 3-4 days post-hCG (Avastin post-hCG; n = 4); 4) COS + Simulated Early Pregnancy (SEP n = 3); or 5) COS + SEP + Avastin (SEP + Avastin n = 3). Follicles were aspirated 36 h post-hCG, fluid was collected from one follicle for analysis of steroid and vascular hormone content. Remaining follicles were aspirated, and luteinized granulosa cells (LGCs) cultured for 24 h. Ovarian/uterine vascular flow (VF) and blood volume (BV) were analyzed by contrast enhanced ultrasound (CEUS) before hCG bolus and 6-8 days post-hCG bolus/time of peak SEP response. Ovarian permeability to albumin was analyzed by Dynamic Contrast Enhanced-MRI (DCE-MRI) post-hCG.
Abdominal fluid was present in 4/5 Control, 2/6 Avastin pre-hCG, and 3/4 Avastin post-hCG females. Neutralization of VEGFA before hCG reduced ovarian VF, BV, and permeability to albumin (P < 0.05), while only ovarian VF and permeability were reduced in Avastin-post hCG group (P < 0.05). There was no effect of Avastin on ovarian vascular function during COS + SEP. VEGF levels in follicular fluid were reduced 78-fold by Avastin pre-hCG, and LGCs exposed to Avastin in vivo also released 4-fold less VEGF into culture media (P < 0.05). Culture medium of LGCs exposed to VEGFA neutralization in vivo had lower levels of P4 and ANGPT1, and an increased ratio of ANGPT2/1 (P < 0.05). Uterine VF was reduced by SEP + Avastin in the basalis/junctional zone (P < 0.05).
Avastin treatment before hCG prevents the development of symptoms associated with ovarian hyperstimulation syndrome. In vitro data suggest neutralization of VEGFA alters expression of other vascular factors typically induced by hCG in the luteinizing follicle. Neutralization of VEGFA action alters the vascular function of the basalis zone of the uterus during simulated early pregnancy, indicating a potential effect on embryo implantation.
卵巢过度刺激综合征(OHSS)是一种与女性控制性卵巢刺激(COS)周期中绒毛膜促性腺激素(hCG)暴露后血清血管内皮生长因子A(VEGFA)升高相关的疾病。在本研究中,我们测试了静脉注射VEGFA中和剂对恒河猴COS周期中OHSS样症状和血管功能的影响。
将猴子(n = 8)采用3种COS方案进行治疗,并随机分为以下几组:1)单纯COS(对照组,n = 5);2)在hCG前19±5小时给予COS + VEGF单克隆抗体阿瓦斯汀(阿瓦斯汀-hCG前;n = 6);3)在hCG后3 - 4天给予COS + 阿瓦斯汀(阿瓦斯汀-hCG后;n = 4);4)COS + 模拟早孕(SEP,n = 3);或5)COS + SEP + 阿瓦斯汀(SEP + 阿瓦斯汀,n = 3)。在hCG后36小时抽吸卵泡,从一个卵泡中收集液体用于分析类固醇和血管激素含量。抽吸剩余卵泡,并将黄体化颗粒细胞(LGCs)培养24小时。在hCG推注前以及hCG推注后6 - 8天/SEP反应峰值时间,通过对比增强超声(CEUS)分析卵巢/子宫血管流量(VF)和血容量(BV)。在hCG后通过动态对比增强磁共振成像(DCE - MRI)分析卵巢对白蛋白的通透性。
4/5的对照组、2/6的阿瓦斯汀-hCG前组和3/4的阿瓦斯汀-hCG后组雌性动物出现腹腔积液。hCG前中和VEGFA可降低卵巢VF、BV和对白蛋白的通透性(P < 0.05),而阿瓦斯汀-hCG后组仅卵巢VF和通透性降低(P < 0.05)。在COS + SEP期间,阿瓦斯汀对卵巢血管功能无影响。阿瓦斯汀-hCG前使卵泡液中的VEGF水平降低78倍,体内暴露于阿瓦斯汀的LGCs向培养基中释放的VEGF也减少4倍(P < 0.05)。体内暴露于VEGFA中和剂的LGCs培养基中孕酮(P4)和血管生成素1(ANGPT1)水平较低,且血管生成素2/1(ANGPT2/1)比值升高(P < 0.05)。SEP + 阿瓦斯汀使基底/交界区的子宫VF降低(P < 0.05)。
hCG前给予阿瓦斯汀可预防与卵巢过度刺激综合征相关症状的发生。体外数据表明,VEGFA的中和改变了通常由hCG在黄体化卵泡中诱导的其他血管因子的表达。VEGFA作用的中和改变了模拟早孕期间子宫基底区的血管功能,表明对胚胎着床有潜在影响。