• 제목/요약/키워드: uterus endometrium

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Serial Ultrasonographic Evaluation of Postpartum Uterine Involution in Miniature Schnauzer Dogs

  • Yeo, Woon-Chang;Kim, Bang-Sil;Yun, Chang-Jin;Park, Chul-Ho;Kim, Jung-Bae;Moon, Jin-San;Suh, Guk-Hyun;Oh, Ki-Seok;Son, Chang-Ho
    • 한국수정란이식학회지
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    • 제22권4호
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    • pp.229-234
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    • 2007
  • This study was undertaken to determine the normal appearance of the postpartum uterine involution. Postpartum changes in uterine shape, architecture, echogenicity and diameter were monitored with ultrasonography in 8 Miniature Schnauzer dogs. Vaginal discharge was observed visually during the 3 weeks of postpartum. A large amount of viscous dark green discharge changed progressively to a small amount of transparent discharge. In the uterine shape, the transverse images were crescent or polygonal at the beginning, but became circular after 16 days. At postpartum day 24, the longitudinal images of placental and interplacental sites were similar to each other The echogenicity of uterine structure was clearly distinguishable among the hyperechoic serous membrane, hypochoic myometrium, hyperechoic endometrium, and anechoic uterine contents during the first week postpartum, but afterward the interluminal boundaries and echogenicity became obscure gradually. In addition, the anechoic substance of the endometrial cavity was not observed after postpartum day 28. In the uterine diameter, the diameter of placental sites decreased markedly from 24 mm at the first day postpartum to 13 mm at day 7, and the diameter of interplacental sites decreased from 15 mm at postpartum day 1 to 10 mm at day 7. At postpartum day 65, the uterus (6.4 mm) changed little and had a uniform homogenous echo, and thus it was confirmed that uterine involution was completed at that time in Miniature Schnauzer dogs.

Differential Expressions of Aquaporin Subtypes in Female Reproductive Tract of Mice

  • Im, Ji Woo;Lee, Chae Young;Kim, Dong-Hwan;Bae, Hae-Rahn
    • 한국발생생물학회지:발생과생식
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    • 제24권3호
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    • pp.177-185
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    • 2020
  • Although many aquaporin (AQP) transcripts have been demonstrated to express in the female reproductive tract, the defined localizations and functions of AQP subtype proteins remain unclear. In this study, we investigated the expression of AQP1, AQP3, AQP5, AQP6, and AQP9 proteins in female reproductive tract of mouse and characterized their precise localizations at the cellular and subcellular levels. Immunofluorescence analyses for AQP1, AQP3, AQP6, and AQP9 showed that these proteins were abundantly expressed in female reproductive tract and that intense immunoreactivities were observed in mucosa epithelial cells with a subtype-specific pattern. The most abundant aquaporin in both vagina and uterine cervix was AQP3. Each of AQP1, AQP3, AQP6, and AQP9 exhibited its distinct distribution in stratified squamous or columnar epithelial cells. AQP9 expression was predominant in oviduct and ovary. AQP1, AQP3, AQP6, and AQP9 proteins were mostly seen in apical membrane of ciliated epithelial cells of the oviduct as well as in both granulosa and theca cells of ovarian follicles. Most of AQP subtypes were also expressed in surface epithelial cells and glandular cells of endometrium in the uterus, but their expression levels were relatively lower than those observed in the vagina, uterine cervix, oviduct and ovary. This is the first study to investigate the expression and localization of 5 AQP subtype proteins simultaneously in female reproductive tract of mouse. Our results suggest that AQP subtypes work together to transport water and glycerol efficiently across the mucosa epithelia for lubrication, proliferation, energy metabolism and pH regulation in female reproductive tract.

자궁체부의 양성 및 악성 종양의 자기공명영상 소견과 감별 진단 (MRI Findings and Differential Diagnosis of Benign and Malignant Tumors of the Uterine Corpus)

  • 김지현;허숙희;신상수;정용연
    • 대한영상의학회지
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    • 제82권5호
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    • pp.1103-1123
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    • 2021
  • 자궁은 크게 자궁체부와 자궁경부로 나뉜다. 이 중 자궁내막과 자궁근층으로 이루어진 자궁체부에는 양성에서 악성 종양까지 다양한 질환이 발생한다. 비침습적인 일차적 평가로 초음파와 컴퓨터단층촬영이 있으나 비특이적인 영상 소견으로 감별이 어려운 경우가 있다. 반면 높은 해상도와 병리학적 특성 파악이 가능한 자기공명영상은 병변의 위치 확인뿐만 아니라 조직학적 특징, 그리고 악성 종양의 병기 설정에도 도움을 준다. 이 종설에서는 영상의학과 의사들이 알아야 할 자궁체부에서 볼 수 있는 다양한 양성과 악성 종양들의 특징적인 자기공명영상 소견들과 이들의 감별점에 대해 정리했다.

진도개에서 분만후 자궁수복의 연속적 초음파상 (Serial ultrasonographic appearance of postpartum uterine involution in Korea Jin-do dogs)

  • 손창호;강병규;최한선;김기원;강현구;신창록;박인철
    • 대한수의학회지
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    • 제39권3호
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    • pp.653-664
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    • 1999
  • This study was undertaken to determine the normal appearance of the postpartum uterine involution. Postpartum changes in uterine shape, architecture, echogenicity and diameter were monitored with ultrasonography in 11 Korea Jin-do dogs. Serial ultrasonographic examination was done daily during the first week, 3 days interval from 8 to 30 days, and weekly from 31 to 100 days postpartum, respectively. Of 11 postpartum bitches, 10 bitches (90.9%) had normal involution and 1 bitch (9.1%) had subinvolution of the placental sites (SIPS) by gross findings, vaginal discharges, and by ultrasographic findings, uterine shape and echogenicity. The excretory period of vaginal discharges in 10 normal bitches of uterine involution was finished completely at $20.2{\pm}4.6$ days (Mean${\pm}$SD) postpartum, but in 1 SIPS at 50 days postpartum. The short axis shape of the uterus was initially often flaccid-appearing. It varied from circular to crescent shaped to polygonal. This lasted until $16.5{\pm}3.7$ days postpartum, during which time the short axis uterine shape gradually changed to circular. Also, the long axis shape of the uterus was created a beaded appearance of the horns until $29.9{\pm}3.2$ days postpartum. After 30 days, it was appeared as tubular shape without distinguished between placental and interplacental sites. The ultrasonographic image of the postpartum uterus consisted of four echogenicity distinct layers. Uterine wall was represented the very hyperechoic serosa, hypoechoic myometrium, hyper echoic endometrium and anechoic structures of fluid in the uterine cavity until 7 days postpartum. The individual uterine layers were most prominent during the first week postpartum, and they became progressively less distinct throughout the course of uterine involution. Anechoic structures of fluid in the uterine cavity was detected until $25.0{\pm}6.4$ days postpartum, after which time it was not reliably detected. The uterine diameter was decreased not only in the placental sites frorm $24.1{\pm}2.5mm$ at 1 day to $15.4{\pm}1.4mm$ at 7 days postpartum, but also in the interplacental sites $14.9{\pm}1.5mm$ at 1 day, $10.6{\pm}0.8mm$ at 7 days postpartum. There was a general trend of decreasing uterine diameter, which occurred more rapidly at the placental sites. At 31 days pastpartum, these diameter reached almost same size, after that time, they could be not distinguished between placental and interplacental sites. At 87 days postpartum, the uterine diameter was $5.6{\pm}0.6mm$ both placental and interplacental sites, and the uterine horns were uniform hypoechoic, tubular structures without enlargement. Therefore, complete involution of the uterus occurred at that time. It was concluded that normal postpartum uterine involution in Korea Jin-do bitches appeared to be completed around 87 days postpartum by gross findings such as vaginal discharges, and by ultrasonographic findings, uterine shape and echogenicity. Also ultrasonographic characteristics of the postpartum uterine involution were described. Therefore, these result suggest that ultrasonographic assessment is a reliable method for diagnosing the SIPS and uterine dysfunction, such as pyometra in bitch.

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흰쥐의 난소기능(卵巢機能)이 갑상선(甲狀腺), 부현(副賢) 및 자궁(子宮)에 미치는 영향(影響) (Effects of Ovarian Function on the Thyroid Gland, Adrenal Gland and Uterus in Female Rats)

  • 서길웅;김종섭;박창식;이규승
    • 농업과학연구
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    • 제17권1호
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    • pp.34-44
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    • 1990
  • 난소(卵巢)의 기능(機能)이 갑상선(甲狀腺), 부현(副賢) 및 자궁(子宮)에 미치는 영향(影響)을 구명(究明)하기 위하여 성숙(成熟) 암흰쥐 144마리를 난소척출군(卵巢剔出群)(Ovx.), Estradiol(Est.) 처리군(處理群) 및 정상대조군(正常對照群)의 3개군(個群)으로 나누어 48마리씩 배치(配置)한 다음 난소척출군(卵巢剔出群)에서는 양측난소(兩側卵巢)를 완전(完全)히 척출(剔出)하였고 Est.처리군(處理群)에서는 마리당 $200{\mu}g$의 estradiol benzoate를 48시간(時間) 간격(間隔)으로 주사(注射)하였다. 각(各) 군별(群別)로 처리후(處理後) 시간경과(時間經過)에 따라 3, 6, 12, 18 및 24시간후(時間後)와 5, 10 및 15일후(日後)에 각각(各各) 6마리씩 도살(屠殺)하여 혈청중(血淸中)의 estradiol-$17{\beta}$와 progesterone의 농도변화(濃度變化)를 측정(測定)하였고 아울러 갑상선(甲狀腺), 부현(副賢) 및 자궁(子宮)의 중량측정(重量測定) 및 조직적(組織的) 검색(檢索)을 실시(實施)하여 비교검토(比較檢討)한 바 다음과 같은 결론(結論)을얻었다. 1. estradiol-$17{\beta}$의 혈청중(血淸中) 농도변화(濃度變化)는 난소척출군(卵巢剔出群)에서는 급속(急速)히 감소(減少)하여 처리(處理 )18시간후(時間後)부터는 27.20pg/ml 이하(以下)의 수준(水準)이었으며 Est.처리군(處理群)에서는 處理後(처리후) 18시간(時間)까지는 급증(急增)하였고 그 후(後)로는 약간 낮은 농도(濃度)를 보였다. 2. progesterone의 혈청중(血淸中) 농도변화(濃度變化)는 난소척출군(卵巢剔出群)과 Est.처리군(處理群)에서 다같이 정상대조군에(正常對照群) 비(比)하여 모든 관찰시간(觀察時間)에서 유의성(有意性)이 인정(認定)되는 감소(減少)를 하였는데 난소척출군(卵巢剔出群)에서 최소치(最小値)를 나타냈다. 3. 갑상선(甲狀腺)의 중량(重量)은 처리(處理) 5일후(日後)부터 난소척출군(卵巢剔出群)은 정상대조군(正常對照群)에 비하여 감소(減少)되는 경향(傾向)이었고 Est.처리군(處理群)은 증가(增加)되는 경향(傾向)이었으나, 유의성(有意性)은 처리후(處理後) 10일(日)과 15일(日)에서만이 인정(認定)되었다. 4. 갑상선(甲狀腺)의 조직소견(組織所見)은 난소척출군(卵巢剔出群)에서는 처리(處理) 5일후(日後)부터 여포상피세포(濾胞上皮細胞)가 편평화(扁平化)되기 시작하였는데 10일후(日後)부터는 핵농축(核濃縮), 15일후(日後)는 핵붕괴현상(核崩壞現像)을 동반(同伴)하였다. 그러나Est.처리군(處理群)에서는 처리(處理) 10일후(日後)부터 여포상피세포(濾胞上皮細胞)가 비대(肥大)되면서 원주화(圓柱化)되는 조직소견(組織所見)이었다. 5. 부현(副賢)의 중량(重量)은 처리후(處理後) 10일(日)과 15일후(日後)에서만이 비교군간(比較群間)에 유의성(有意性)이 인정(認定)되었는데 난소척출군(卵巢剔出群)은 정상대조군(正常對照群)에 비하여 낮은 값을 보였고 Est.처리군(處理群)은 무거운 중량치(重量値)를 나타냈다. 6. 부현(副賢)의 조직상(組織像)은 난소척출군(卵巢剔出群)에서는 처리(處理) 10일후(日後)부터 색상대(索狀帶)와 망상대(網狀帶)의 세포(細胞)가 핵농축(核濃縮)을 동반(同伴)하면서 위축(萎縮)되었고 Est.처리군(處理群)에서는 처리(處理) 5일후(日後)부터 색상대(索狀帶)와 망상대(網狀帶)의 세포(細胞)가 비대(肥大)되기 시작하는 조직소견(組織所見)올 보였으나 구상대(球狀帶)와 수질(髓質)에서는 어떠한 변화(變化)도 인지(認知)되지 않았다. 7. 자궁(子宮)의 중량(重量)은 모든 관찰시간(觀察時間)에서 비교군간(比較群間에 유의성(有意性)이 인정(認定)되었는데 난소척출군(卵巢剔出群)은 정상대조군(正常對照群)에 비하여 급속(急速)히 감소(減少)되었고 Est.처리군(處理群)은 급격(急激)히 증가(增加)되었다. 8. 자궁(子宮)의 조직상(組織像)은 난소척출군(卵巢剔出群)에서는 처리(處理)1/2일후(日後)부터 자궁점막상피(子宮粘膜上皮)와 점막고유층(粘膜固有層)이 1일후(日後)부터는 자궁근층(子宮筋層)이 위축(萎縮)되는 퇴행성(退行性) 변화(變化)가 일어나기 시작하여 실험기간(實驗期間)이 경과(經過) 할수록 급속(急速)히 진행(進行) 되었으며, Est.처리군(處理群)에서는 처리(處理)1/2일(日)부터 자궁(子宮)의 각층(各層)이 증식(增殖) 비대(肥大)되는 조직소견(組織所見)올 보였다.

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스테로이드 호르몬이 생쥐 자궁내막에서 Aquaporin-4, -5와 -8 유전자의 발현과 존재부위에 미치는 영향 (Effect of Steroid Hormones on Expression and Localization of Aquaporin-4, -5 and -8 Genes in Mouse Uterine Endometrium)

  • 강수만;강한승;계명찬;신현상;이지원;이성은;김문규
    • Clinical and Experimental Reproductive Medicine
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    • 제31권2호
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    • pp.119-131
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    • 2004
  • 연구 목적: 난소에서 분비되는 스테로이드 호르몬인 에스트로젠과 프로게스테론은 포유동물의 생식기관 발달과 정상적인 생식 기능, 수정과 배아의 착상에 중요한 역할을 한다. 특히 에스트로젠은 자궁내액을 내강으로 분비하여 자궁부종 기작에 중요한 역할을 한다. 자궁내액은 정자의 수정능력 획득과 착상전 배아의 발달에 매우 중요하다. Aquaporin (AQP)은 막관통 물수송 단백질로서 여러 조직에 넓게 분포되어 있으며, 세포간 또는 상피세포간 물의 이동에 중요한 역할을 한다. 본 연구에서는 생쥐 자궁에서 스테로이드 호르몬에 의해 조절되는 자궁내액의 이동에 AQP 유전자가 관여하는지를 알아보았다. 연구 재료 및 방법: 난소 절제술을 시행한 생쥐에 스테로이드 호르몬을 피하주사하고 6, 12, 24시간 간격으로 자궁조직을 적출하였다. 대조군은 sesame oil만을 주사한 후 6시간째에 수획한 자궁조직을 사용하였으며, 실험군은 시간대별과 스테로이드 처리별로 채취한 자궁조직에서 역전사중합효소반응을 수행하였다. 역전사중합효소반응을 통해 막관통 단백질인 AQP-4, -5, -8 mRNA의 발현양상을 살펴보았다. 또한 mRNA의 위치를 살펴보기 위해 laser microdissection을 이용하여 RT-PCR을 수행하였다. 마지막으로 자궁조직내에서의 단백질 발현 부위를 관찰하기 위해 면역조직화학염색을 실시하였다. 결 과: AQP-4, -5, -8 mRNA은 프로게스테론을 처리한 군보다 에스트로젠을 처리한 군에서 많이 발현되었으며, 에스트로젠을 주사한 지 6시간째 발현정도를 대조군과 비교할 때 AQP-4, -5, -8 mRNA가 각각 7.9배, 2.8배, 3.8배로 나타났다. AQP-4, -5, -8 mRNA는 간충조직보다 자궁내 상피조직에서 스테로이드 호르몬의 영향을 받아 발현양상의 차이가 나타났으며, 주로 에스트로젠의 영향을 받아 발현이 증가하였다. AQP-4 단백질은 에스트로젠을 24시간 처리한 후 프로게스테론을 처리한 군의 자궁내 상피조직에서 많이 발현되었으며, AQP-5와 -8 단백질은 에스트로젠을 처리한 군의 자궁내 상피조직에서 발현이 증가하였다. 결 론: 이상의 결과를 통해 AQP-4, -5, -8은 주로 에스트로젠에 의해 자궁내 상피세포에서 발현이 증가되는 것으로 보아 에스트로젠의 영향하에 일어나는 자궁내액의 이동으로 인한 자궁부종기작에 이동통로로서 관여하는 것으로 사료된다.

17β-Estradiol이 progesterone target cell 분포에 미치는 영향에 대한 면역조직화학적 연구 I. 방사선자기법을 이용한 target cell의 분포에 대하여 (Immunohistochemical study on distribution of progesterone target cells by 17β-Estradiol I. Distribution of progesterone target cells by autoradiography)

  • 곽수동;고필옥;김종섭
    • 대한수의학회지
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    • 제36권1호
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    • pp.93-99
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    • 1996
  • This study was designed to investigate the effect of estrogen(Est) on the progestcrone(Prog) target cells by autoradiography. The spayed 16 mice(ICR, approximately 18~25g) were randomly alloted into 3 groups. $^3H$-Prog-treated group were injected with $40{\mu}Ci$ of $^3H$-Prog/mouse/day for 1 day, Est + $^3H$-Prog-treated group with $20{\mu}Ci$ of $17{\beta}$-Est/mouse/day for 3 days and then with $40{\mu}Ci$ of $^3H$-Prog/mouse at 4th day, and Est+$^3H$-thymidine(TdR)-treated group with $20{\mu}g$ of $17{\beta}$-Est/mouse/day for 3 days and then $80{\mu}Ci$ of $^3H$-TdR/mouse at 4th days. 1. Mice uteri of both Est+$^3H$-Prog-treated group and Est+$^3H$-TdR-treated group were hypemophied in gross finding and the endometrium and myometrium were thickened in microscopic findings. These findings were confirmed that Est enlarged the uteri of mice. 2. Cryo-preparations of mice organs were processed for autoradiography using Kodak NTB-2 emulsion following Kodak D-19 developer and hematoxylin counterstain. In each group, the number values of silver grain distribution appeared to be higher in the $^3H$-Prog-treated group than in the Est+$^3H$-Prog-treated group. It was considered that Est and Prog inhibit each other in action. 3. In both $^3H$-Prog-treated group and Est+$^3H$-Prog-treated group, the uteri have highest distribution rates of silver grains than in other organs, and the cerebral neurons, hepatocytes, bronchiolar epithelial cells and splenic reticular cells also contained some silver grains. 4. The orders of the cell types with more number of silver grains in the uteri were stromal cells, glandular epithelial cells, luminal surface cells and muscular cells and also were as above orders in distribution of proliferating cell type by $^3H$-TdR.

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착상 및 태반 발달과정에 따른 영양막세포의 역할 (Role of Trophobolast in Implantation and Placenta Development)

  • 김기진
    • Clinical and Experimental Reproductive Medicine
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    • 제37권3호
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    • pp.181-189
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    • 2010
  • 태반 (placenta)은 임신기간 동안에만 존재하는 태아유래 일시적인 기관으로, 모체와 태아간의 정확한 조절 기전을 통해 태아의 발달을 수행하는 중요한 기관이다. 영양막세포 (trophoblast)는 임신 초기 빠른 분열 및 분화 과정을 거쳐 태반을 형성하는 주요 세포이다. 영양막세포의 역할은 초기 배아 착상 시기부터 40주간의 임신기간 동안 태반의 형성 과정에서 다양하게 변화된다. 착상은 모체 자궁내막층으로의 포배의 가장 밖에 존재하는 분화된 영양막세포(예, 합포영양막세포)의 침윤에 의해 이루어진다. 또한, 영양막세포은 임신기간 동안 배아의 성숙과 발달에 필요한 영양분과 노폐물 등을 모체와 태아 양방향으로 적절하게 전달할 뿐 아니라 태반 내에서 침윤과 다양한 물질들의 합성 혹은 분비에 관련된 대사작용에 관여한다. 이 기간 동안 영양막세포의 기능 이상은 태아의 선천적인 기형뿐 아니라 자간전증 등을 포함하는 다양한 산과질환을 유발하기도 한다. 그러므로, 영양막세포는 태반과 태아의 발달에 결정적인 요인으로 작용한다. 본 고찰에서는 다양한 영양막세포들의 기능을 이해하기 위해 분류 및 그 종류별 특징 등을 살펴보고, 착상 단계와 태반 발달에 따른 영양막세포의 고유한 역할에 대해 알아보고 향후 활용될 수 있는 연구 분야에 대해 알아보고자 한다.

Vero Cell과의 공동배양이 체외에서 생쥐 배아발생에 미치는 영향 (The Effects of Vero Cell Co-culture on Mouse Embryo Development)

  • 이윤;박준홍;강혜나;김용봉;이응수;박성관
    • Clinical and Experimental Reproductive Medicine
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    • 제24권2호
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    • pp.233-239
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    • 1997
  • Embryos of most mammalian species grown in vitro would undergo developmental arrest at the approximate time of genomic activation. Stage-specific cell block and the resulting rapid loss of embryo viability in conventional culture media have limited the duration for which embryos may be cultured prior to transfer. As a result, embryos are usually transferred to the uterus at the 4-to 8-cell stage to avoid the loss of viability associated with long-term in vitro culture. Early transfer has led to asynchrony of the endometrium-trophectoderm interaction at the time of implantation and a resultant reduction in the rate of implantation. To overcome these problems, a variety of co-culture systems has been devised in which embryos can develop for a longer period prior to embryo transfer. Vero cells, derived from African green monkey kidney, share a common embryologic origin with cells from the genital tract. In addition, they are potentially safe to use, since they are highly controlled for viruses and other contaminants. Therefore, co-culture using Vero cells has been widely utilized to enhance embryo viability and development, although not without controversies. We thus designed a series of experiments to demonstrate whether Vero cells do indeed enhance mouse embryo development as well as to compare the efficacy of co-culturing mouse 1-cell embryos on Vero cell monolayer in both Ham's F-10 and human tubal fluid (HTF) culture media. 1-cell stage ICR mouse embryos were cultured either in the presence of Vero cells (Group A) or in conventional culture medium alone (Group B). In Ham's F-10 significantly more 3-to-8cell embryos developed in group A than group B (59.8 versus 10.0%; p<0.01). In contrast, there was no significant difference in embryonic development both group A and group B in HTF. However, significant differences were noted only in later embryonic stage (13 and 0%; p<0.05 of group A and B respectively, hatching or hatched). In Ham's F-10, we also could observe the beneficial effect of Vero cell on hatching process (70.7 and 42.1%; p<0.05 of group A and group B respectively).

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Effects of dietary supplementation of glucose oxidase, catalase, or both on reproductive performance, oxidative stress, fecal microflora and apoptosis in multiparous sows

  • Sun, Xiaojiao;Piao, Longguo;Jin, Haifeng;Nogoy, K. Margarette C.;Zhang, Junfang;Sun, Bin;Jin, Yi;Lee, Dong Hoon;Choi, Seong-Ho;Smith, Stephen B;Li, Xiangzi
    • Animal Bioscience
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    • 제35권1호
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    • pp.75-86
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    • 2022
  • Objective: The objective of this experiment was to investigate the effect of dietary glucose oxidase (GOD), catalase (CAT), or both supplementation on reproductive performance, oxidative stress, and apoptosis in sows. Methods: A total of 104 multiparous sows were randomly assigned to four groups (n = 26) with each group given a basal diet, basal diet plus GOD at 60 U/kg, basal diet plus CAT at 75 U/kg, and basal diet plus GOD at 60 U/kg and CAT at 75 U/kg. Sows were fed the experimental diets throughout gestation and lactation. Results: Dietary GOD supplementation increased average daily feed intake of sows and litter weight at weaning (p<0.05). Dietary CAT supplementation reduced the duration of parturition, stillbirth, and piglet mortality and increased growth performance of weaned piglets (p<0.05). Dietary GOD and CAT supplementation enhanced antioxidant enzyme activities and lessened oxidative stress product levels in plasma of sows and elevated antioxidant capacity of 14-day milk and plasma in weaned piglets (p<0.05). Dietary GOD supplementation increased fecal Lactobacillus counts and reduced Escherichia coli counts of sows (p<0.05). Compared with the basal diet, the GOD diet reduced fecal Escherichia coli counts of sows, but the addition of CAT did not reduce Escherichia coli counts in the GOD diet. Dietary GOD and CAT supplementation reduced the apoptosis rate of the liver, endometrium, and ovarian granulosa cells in sows (p<0.05). In the liver, uterus, and ovary of sows, the mRNA expression of caspase-3 and caspase-9 was downregulated by dietary GOD and CAT supplementation (p<0.05). Conclusion: Dietary GOD and CAT supplementation could improve the antioxidant capacity of sows and weaned piglets, and alleviate hepatic, ovarian and uterine apoptosis by weakening apoptosis-related gene expression. Glucose oxidase regulated fecal microflora of sows, but supplementation of CAT to GOD could weaken the inhibitory effect of GOD on fecal Escherichia coli.