Changes in Uterine Microvessels as a Possible Pathogenic Factor in the Development of Adenomyosis Induced by Pituitary Grafting in Mice.
This study found that pituitary grafting in mice induced adenomyosis and significantly altered uterine microvessels, increasing dilated venules while decreasing overall microvessel numbers.
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The study quantitatively evaluated uterine microvascular changes during experimental adenomyosis development in mice using immunohistochemistry for von Willebrand factor after pituitary grafting. In all pituitary-grafted mice, slight adenomyosis near the mesometrium was observed 4 weeks post-operation, and uteri with adenomyosis showed significantly increased vessel surface area and minor axis in the endometrium with a tendency toward increased values in the myometrium, while the number of blood vessels decreased significantly in both endometrium and myometrium compared with normal uteri. Dilated venules in the endometrium were frequently found, and regional differences were noted in both control and pituitary-grafted animals. The paper concludes that pituitary grafting significantly increased dilated venules and decreased microvessel number, supporting vascular changes as a possible etiological factor in adenomyosis, relating directly to adenomyosis through its mouse model of experimentally induced adenomyosis.
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References (18)
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Cited by (7)
- Magnetic Resonance Imaging-guided Focused Ultrasound Surgery in a Swine Adenomyosis Model 2023
- Experimental adenomyosis 2006
- Probucol, a hypocholesterolemic agent, prevents the development of uterine adenomyosis induced by pituitary grafting in mice. 2004
- Increase in the number of integrinβ1-immunoreactive monocyte-lineage cells in experimentally-induced adenomyosis in mice 2003
- Effects of angiogenesis inhibitor TNP-470 on the development of uterine adenomyosis in mice 2003
- Adenomyosis—A Result of Disordered Stromal Differentiation 2001
- Suppression of the Development of Experimentally Induced Uterine Adenomyosis by a Novel Matrix Metalloproteinase Inhibitor, ONO-4817, in Mice 2001
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