Enhanced Colon Regeneration in Ulcerative Colitis via Mesenchymal Stem Cell Medium and 17-β Estradiol.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
추출되지 않음
I · Intervention 중재 / 시술
intraperitoneal injections of 200 µL CMm derived from 2 × 10 cells or E2-treated CMm three times postinduction
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Histopathological analysis revealed enhanced colon tissue regeneration in these groups. [CONCLUSIONS] These findings suggest that CMm, particularly with E2, may facilitate colonic healing and mitigate inflammation in UC.
[BACKGROUND] Ulcerative colitis (UC), a form of inflammatory bowel disease (IBD), increases the risk of colorectal cancer.
APA
Bakhtiary Z, Hosseinpour Z, Froushani SMA (2026). Enhanced Colon Regeneration in Ulcerative Colitis via Mesenchymal Stem Cell Medium and 17-β Estradiol.. Immunity, inflammation and disease, 14(2), e70387. https://doi.org/10.1002/iid3.70387
MLA
Bakhtiary Z, et al.. "Enhanced Colon Regeneration in Ulcerative Colitis via Mesenchymal Stem Cell Medium and 17-β Estradiol.." Immunity, inflammation and disease, vol. 14, no. 2, 2026, pp. e70387.
PMID
41738392 ↗
Abstract 한글 요약
[BACKGROUND] Ulcerative colitis (UC), a form of inflammatory bowel disease (IBD), increases the risk of colorectal cancer. This study investigates the potential of conditioned medium from mesenchymal stem cells (CMm) treated with 17-beta-estradiol (E2) to enhance colon regeneration in UC-affected rats.
[METHODS] Bone marrow-derived MSCs from male Wistar rats were cultured with 100 nM E2 for 24 h. UC was induced in three groups: colitis (C), mesenchymal stem cells (MSC), and MSCs + estradiol (MSC + E2). Each group received intraperitoneal injections of 200 µL CMm derived from 2 × 10 cells or E2-treated CMm three times postinduction. The study evaluated disease activity index (DAI), myeloperoxidase (MPO) levels, nitric oxide (NO), and pro-inflammatory cytokines (TNF-α, IL-1β, IL-6) in colon tissues, alongside histopathological assessments.
[RESULTS] Results showed significant improvements in DAI and reductions in MPO, NO, and cytokine levels in MSC and MSC + E2 groups compared to the C group. Histopathological analysis revealed enhanced colon tissue regeneration in these groups.
[CONCLUSIONS] These findings suggest that CMm, particularly with E2, may facilitate colonic healing and mitigate inflammation in UC.
[METHODS] Bone marrow-derived MSCs from male Wistar rats were cultured with 100 nM E2 for 24 h. UC was induced in three groups: colitis (C), mesenchymal stem cells (MSC), and MSCs + estradiol (MSC + E2). Each group received intraperitoneal injections of 200 µL CMm derived from 2 × 10 cells or E2-treated CMm three times postinduction. The study evaluated disease activity index (DAI), myeloperoxidase (MPO) levels, nitric oxide (NO), and pro-inflammatory cytokines (TNF-α, IL-1β, IL-6) in colon tissues, alongside histopathological assessments.
[RESULTS] Results showed significant improvements in DAI and reductions in MPO, NO, and cytokine levels in MSC and MSC + E2 groups compared to the C group. Histopathological analysis revealed enhanced colon tissue regeneration in these groups.
[CONCLUSIONS] These findings suggest that CMm, particularly with E2, may facilitate colonic healing and mitigate inflammation in UC.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Animals
- Colitis
- Ulcerative
- Mesenchymal Stem Cells
- Estradiol
- Rats
- Male
- Colon
- Wistar
- Culture Media
- Conditioned
- Regeneration
- Peroxidase
- Nitric Oxide
- Cytokines
- Disease Models
- Animal
- Mesenchymal Stem Cell Transplantation
- Cells
- Cultured
- 17‐beta‐estradiol
- condition medium
- histopathology
- mesenchymal stem cells
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