收藏切换
Research on RIP3-mediated necroptosis promotes penile tissue damage and pharmacological intervention in DMED rats
收藏切换
PDF
Li-pan NIU1, 2, Pei YANG1, Bing-bing ZHU1, 2, Xiu-fang JIN1, 2, Cheng-xia YANG1, 2, Kai-xin LI1, Yu-wei XIA1, Feng-xia LIU1, 2
Chinese Journal of Clinical Pharmacology | 2025, 41(7) : 983 - 988
Less
收藏切换
Chinese Journal of Clinical Pharmacology | 2025, 41(7): 983-988
Clinical and Basic Bridging Research
Research on RIP3-mediated necroptosis promotes penile tissue damage and pharmacological intervention in DMED rats
Full
Li-pan NIU1, 2, Pei YANG1, Bing-bing ZHU1, 2, Xiu-fang JIN1, 2, Cheng-xia YANG1, 2, Kai-xin LI1, Yu-wei XIA1, Feng-xia LIU1, 2
Affiliations
  • 1.Department of Human Anatomy, College of Basic Medicine Science, Xinjiang Medical University, Urumqi 830011, Xinjiang Uygur Autonomous Region, China
  • 2.Xinjiang Key Laboratory of Molecular Biology of Endemic Diseases, Urumqi 830011, Xinjiang Uygur Autonomous Region, China
Published: 2025-04-17 doi: 10.13699/j.cnki.1001-6821.2025.07.016
Outline
收藏切换
Objective

To investigate the role of the receptor-interacting protein kinase 3 (RIP3)-mediated necroptosis pathway in penile tissue damage in diabetes mellitus-induced erectile dysfunction (DMED) rats and the effects of GSK872 and Yimusake intervention in DMED rats.

Methods

Male SD rats with normal sexual function were selected, and diabetic rats were constructed by 2 consecutive days injections of streptozotocin (45 mg·kg-1), DMED rats were screened and randomly divided into model group, experimental group, Yimusake group and combined group. The normal and model groups were injected intraperitoneally with an equal amount of 0.9% NaCl and gavaged with an equal amount of distilled water; the experimental group was injected intraperitoneally with 1 mg·kg-1 GSK872 and gavaged with an equal amount of distilled water; the Yimusake group was injected intraperitoneally with an equal amount of 0.9% NaCl and gavaged with 250 mg·kg-1 Yimusake; the combined group was injected intraperitoneally with 1 mg·kg-1 GSK872 and gavaged with 250 mg·kg-1 Yimusake. The expression of RIP3, mixed lineage kinase domain like protein (MLKL) and transient receptor potential melastatin 7 (TRPM7) were detected by immunohistochemistry and immunofluorescence, α-smooth muscle actin (α-SMA) and Collagen Ⅰ were detected by Western blotting in rat penile tissues.

Results

The positive area ratios of RIP3 in the penile tissues of normal, model, experimental, Yimusake and combined groups were (7.71±1.92)%, (35.72±2.73)%, (20.20±2.51)%, (19.94±2.66)% and (9.31±1.98)%; MLKL positive area ratios were (7.39±1.73)%, (26.48±1.74)%, (15.66±1.87)%, (15.88±1.59)% and (8.45±1.65)%; TRPM7 positive area ratios were (6.43±2.10)%, (35.77±1.78)%, (23.76±1.79)%, (25.24±2.08)% and (9.39±1.72)%; α-SMA protein relative expression levels were 1.53±0.13, 0.39±0.08, 0.88±0.14, 0.86±0.12 and 1.52±0.12; Collagen Ⅰ protein relative expression levels were 0.29±0.10, 1.20±0.14, 0.73±0.07, 0.71±0.11 and 0.31±0.10. The differences between the above indices in the model group compared with the normal group, the above indices in the experimental group compared with the model group, the above indices in the Yimusake group compared with the model group and the above indices in the combined group compared with the model group were all statistically significant (all P<0.05).

Conclusion

RIP3/MLKL/TRPM7 necroptosis pathway may participate in regulating the progression of DMED rats by promoting cell death and fibrosis, while GSK872 and Yimusake may ameliorate penile injury in rats by inhibiting this pathway.

Yimusake tablet  /  GSK872  /  receptor-interacting protein kinase 3/mixed lineage kinase domain like protein /transient receptor potential melastatin 7  /  necroptosis  /  diabetes mellitus-induced erectile dysfunction
Li-pan NIU, Pei YANG, Bing-bing ZHU, Xiu-fang JIN, Cheng-xia YANG, Kai-xin LI, Yu-wei XIA, Feng-xia LIU. Research on RIP3-mediated necroptosis promotes penile tissue damage and pharmacological intervention in DMED rats[J]. Chinese Journal of Clinical Pharmacology, 2025 , 41 (7) : 983 -988 . DOI: 10.13699/j.cnki.1001-6821.2025.07.016
Year 2025 volume 41 Issue 7
PDF
0
0
Cite this Article
BibTeX
Article Info
doi: 10.13699/j.cnki.1001-6821.2025.07.016
  • Receive Date:2024-10-23
  • Online Date:2026-08-04
  • Published:2025-04-17
Article Data
Affiliations
History
  • Received:2024-10-23
Funding
Affiliations
    1.Department of Human Anatomy, College of Basic Medicine Science, Xinjiang Medical University, Urumqi 830011, Xinjiang Uygur Autonomous Region, China
    2.Xinjiang Key Laboratory of Molecular Biology of Endemic Diseases, Urumqi 830011, Xinjiang Uygur Autonomous Region, China
References
Share
https://castjournals.cast.org.cn/joweb/zglcylxzz/EN/10.13699/j.cnki.1001-6821.2025.07.016
Share to
QR

Scan QR to access full text

Cite this article
BibTeX
Citations
表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
关闭全屏
  • BibTeX
  • EndNote
  • RefWorks
  • TxT