Lebovic Dan I, Mwenda Jason M, Chai Daniel C, Mueller Michael D, Santi Allessandro, Fisseha Senait, D'Hooghe Thomas
Reproductive Endocrinology Division, Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Fertil Steril. 2007 Oct;88(4 Suppl):1108-19. doi: 10.1016/j.fertnstert.2006.12.072. Epub 2007 May 11.
To determine the effects of a thiazolidinedione (TZD) agonist of peroxisome proliferator-activated receptor (PPAR)-gamma, rosiglitazone, in a baboon model of established endometriosis.
Prospective, randomized, placebo-controlled study.
Experimental surgery laboratory at the Institute of Primate Research in Nairobi, Kenya.
ANIMAL(S): Endometriosis was induced using intrapelvic injection of eutopic menstrual endometrium in 12 female baboons with a normal pelvis that had undergone at least one menstrual cycle since the time of captivity.
INTERVENTION(S): Induction of endometriosis by laparoscopy was performed in 12 baboons with a normal pelvis. Endometrial tissue was extracted from each baboon by curettage, and a standard amount of endometrium was then seeded onto several peritoneal sites. About 34-68 days after the induction of laparoscopy, a pretreatment laparoscopy (baseline disease assessment) was performed in the baboons to record the extent of endometriotic lesions. The 12 baboons were randomized into three groups and treated from the day after the staging laparoscopy for a total duration of 30 days. They received phosphate-buffered saline tablets (n = 4, placebo control; placebo tablets once a day by mouth for 30 days), GnRH-antagonists (n = 4, active control; ganirelix acetate 125 microg/day for 30 days), or rosiglitazone (n = 4, test drug, 2 mg by mouth each day for 30 days). A third and final laparoscopy on day 30 after the start of treatment was performed to record the extent of endometriosis. The type of lesion (typical, red, white, or suspicious) was recorded. Biopsies were obtained to confirm the histological presence of endometriosis.
MAIN OUTCOME MEASURE(S): A videolaparoscopy was performed 30 days after treatment to document the number and surface area of endometriotic lesions as well as to calculate the revised American Society for Reproductive Medicine score and stage.
RESULT(S): The surface area of endometriotic lesions was statistically significantly lower in rosiglitazone-treated baboons when compared with the placebo group. Baboons treated with rosiglitazone or ganirelix had a greater negative relative change in surface area of peritoneal endometriotic lesions than controls. The overall weighted appearance of the lesion types suggests that rosiglitazone may deter the development of newer endometriotic lesions.
CONCLUSION(S): A PPAR-gamma ligand, rosiglitazone, effectively diminishes the burden of endometriosis disease in a baboon endometriosis model. This animal model holds promise that a TZD drug may be helpful in women with endometriosis.
在已建立的狒狒子宫内膜异位症模型中,确定过氧化物酶体增殖物激活受体(PPAR)-γ的噻唑烷二酮(TZD)激动剂罗格列酮的作用。
前瞻性、随机、安慰剂对照研究。
肯尼亚内罗毕灵长类动物研究所的实验外科实验室。
对12只骨盆正常且自圈养以来至少经历过一个月经周期的雌性狒狒,通过盆腔内注射在位月经子宫内膜诱导子宫内膜异位症。
对12只骨盆正常的狒狒进行腹腔镜下子宫内膜异位症诱导。通过刮宫从每只狒狒中提取子宫内膜组织,然后将标准量的子宫内膜接种到几个腹膜部位。在腹腔镜诱导后约34 - 68天,对狒狒进行预处理腹腔镜检查(基线疾病评估),以记录子宫内膜异位病变的程度。12只狒狒被随机分为三组,从分期腹腔镜检查后的第二天开始治疗,共持续30天。它们分别接受磷酸盐缓冲盐片(n = 4,安慰剂对照;安慰剂片每天口服一次,共30天)、GnRH拮抗剂(n = 4,活性对照;醋酸加尼瑞克125微克/天,共30天)或罗格列酮(n = 4,受试药物,每天口服2毫克,共30天)。在治疗开始后第30天进行第三次也是最后一次腹腔镜检查,以记录子宫内膜异位症的程度。记录病变类型(典型、红色、白色或可疑)。获取活检样本以确认子宫内膜异位症的组织学存在。
治疗30天后进行视频腹腔镜检查,记录子宫内膜异位病变的数量和表面积,并计算修订后的美国生殖医学学会评分和分期。
与安慰剂组相比,罗格列酮治疗的狒狒中子宫内膜异位病变的表面积在统计学上显著降低。用罗格列酮或加尼瑞克治疗的狒狒腹膜子宫内膜异位病变表面积的相对变化比对照组更大。病变类型的总体加权外观表明罗格列酮可能会抑制新的子宫内膜异位病变的发展。
PPAR-γ配体罗格列酮在狒狒子宫内膜异位症模型中有效减轻了子宫内膜异位症疾病的负担。这个动物模型表明TZD药物可能对患有子宫内膜异位症的女性有帮助。