Chu Py Po-yin, Salamonsen L A, Lee C S, Wright P J
Department of Veterinary Science, The University of Melbourne, 250 Princes Hwy, Werribee, Victoria 3030, Australia.
Reproduction. 2002 Mar;123(3):467-77.
The relationships between activities of matrix metalloproteinases (MMPs) in the canine uterus and the occurrence of degeneration of the luminal epithelium, cystic endometrial hyperplasia, pyometra and uterine remodelling post partum were determined. Mature bitches (n = 10) were ovariectomized, treated with hormones (oestradiol benzoate, progestagen) and investigated at stages simulating pro-oestrus (n = 2), oestrus (n = 2), dioestrus (n = 2), and mid- (n = 2) and late (n = 2) anoestrus (3 and 9 weeks, respectively, after cessation of treatment with progestagen). Untreated bitches (n = 1 per group) served as controls (Expt 1). An additional 10 ovariectomized bitches, at the end of treatment-induced simulated dioestrus, were treated each day for a further 3 weeks either with the same dose (standard dose, n = 3), a decreased dose (n = 3) or an increased dose (n = 3) of progestagen, or no treatment (withdrawal dose, n = 1). These bitches were then investigated (Expt 2). A suture was placed in the lumen of one uterine horn of another five bitches at ovariectomy. Three of these bitches were treated to induce simulated dioestrus and two bitches served as untreated controls. In the hormone-treated bitches, the suture resulted in cystic endometrial hyperplasia in one bitch and in cystic endometrial hyperplasia with pyometra in two bitches. The control bitches showed no cystic endometrial hyperplasia or pyometra (Expt 3). Four intact bitches were studied at 2 (n = 1), 3 (n = 2) and 11 (n = 1) weeks post partum. Uterine tissues were also collected from two bitches with naturally occurring cystic endometrial hyperplasia with pyometra (Expt 4). All uteri were examined histologically and the activities of MMP-2, -7 and -9 (latent and active forms) were assessed using zymography of extracts of endometrium. In Expts 1 and 2, marked degeneration of the luminal epithelium in six of 25 bitches (simulated mid-anoestrus, withdrawal dose and decreased dose groups) was not associated with changes in MMP activities. Markedly increased activities of MMP-2 (active form), -7 (latent form) and -9 (active and latent forms) were observed in the bitches with cystic endometrial hyperplasia with pyometra (but not with cystic endometrial hyperplasia alone) and in the bitches at 2 and 3 weeks post partum (but not at 11 weeks post partum). These results indicate that MMPs are not involved with degeneration of the luminal epithelium, but are involved with uterine remodelling in the postpartum bitch and with cystic endometrial hyperplasia with pyometra.
确定了犬子宫中基质金属蛋白酶(MMPs)的活性与腔上皮变性、囊性子宫内膜增生、子宫蓄脓以及产后子宫重塑之间的关系。将成熟母犬(n = 10)进行卵巢切除,用激素(苯甲酸雌二醇、孕激素)处理,并在模拟发情前期(n = 2)、发情期(n = 2)、发情后期(n = 2)以及发情间期中期(n = 2)和后期(n = 2)(分别在停止孕激素处理后3周和9周)进行研究。未处理的母犬(每组n = 1)作为对照(实验1)。另外10只卵巢切除的母犬,在处理诱导的模拟发情后期结束时,每天再用相同剂量(标准剂量,n = 3)、降低剂量(n = 3)或增加剂量(n = 3)的孕激素处理3周,或不处理(撤药剂量,n = 1)。然后对这些母犬进行研究(实验2)。在另外5只母犬卵巢切除时,在一个子宫角的腔内放置缝线。其中3只母犬经处理诱导模拟发情后期,2只母犬作为未处理对照。在激素处理的母犬中,缝线导致1只母犬出现囊性子宫内膜增生,2只母犬出现囊性子宫内膜增生伴子宫蓄脓。对照母犬未出现囊性子宫内膜增生或子宫蓄脓(实验3)。对4只未绝育母犬在产后2周(n = 1)、3周(n = 2)和11周(n = 1)进行研究。还从2只自然发生囊性子宫内膜增生伴子宫蓄脓的母犬采集子宫组织(实验4)。对所有子宫进行组织学检查,并使用子宫内膜提取物的酶谱法评估MMP - 2、- 7和- 9(潜伏和活性形式)的活性。在实验1和2中,25只母犬中的6只(模拟发情间期中期、撤药剂量和降低剂量组)出现的明显腔上皮变性与MMP活性变化无关。在患有囊性子宫内膜增生伴子宫蓄脓的母犬(但不包括仅患有囊性子宫内膜增生的母犬)以及产后2周和3周的母犬(但不包括产后11周的母犬)中,观察到MMP - 2(活性形式)、- 7(潜伏形式)和- 9(活性和潜伏形式)的活性明显增加。这些结果表明,MMPs不参与腔上皮的变性,但参与产后母犬的子宫重塑以及囊性子宫内膜增生伴子宫蓄脓。