Evidence map›Paper›PMID 39344111›Full record

ArticleThe world journal of men's health2025

Blocking TSP1 Ameliorates Diabetes Mellitus-Induced Erectile Dysfunction by Inhibiting the TGF-β/SMAD Pathway.

Mancheng Xia, Yiming Yuan, Dong Fang, Xiaohui Tan, Fangzhou Zhao, Xinfei Li, Pengchao Gao, Zhuo Zhou, Tiegui Nan, Zhongcheng Xin and 2 more

Abstract read
In one paragraph

Article in The world journal of men's health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Mancheng Xia *Department of Urology, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-9209-7246
Yiming Yuan *Department of Urology, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-8312-0723
Dong FangDepartment of Urology, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0001-6746-6559
Xiaohui TanDepartment of Urology, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0003-4139-8716
Fangzhou ZhaoDepartment of Urology, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0001-8109-8916
Xinfei LiDepartment of Urology, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-4201-2443
Pengchao GaoState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.ORCID https://orcid.org/0009-0001-9650-0901
Zhuo ZhouDepartment of Urology, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0009-0002-1396-6085
Tiegui NanState Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.ORCID https://orcid.org/0000-0003-1325-6382
Zhongcheng XinMale Reproductive and Sexual Medicine, Department of Urology, the Second Hospital of Tianjin Medical University, Tianjin, China.ORCID https://orcid.org/0000-0002-0361-2737
Xuesong LiDepartment of Urology, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0002-7030-0856
Ruili GuanDepartment of Urology, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0003-0422-846X

Funding

Beijing Natural Science Foundation 7222189National Natural Science Foundation of China 82001534
6 · The paper itself

Abstract

purposeTo examine the role and mechanism of thrombospondin-1 (TSP1) in the development of fibrosis in diabetes mellitus-induced erectile dysfunction (DMED). MATERIALS AND

methodsDMED was induced by intraperitoneal streptozotocin injection. All rats were categorized into three groups: control group (n=8), DMED group (n=8) and DMED+Leu-Ser-Lys-Leu (LSKL) group (n=8). After eight weeks following the induction of diabetes mellitus, the DMED+LSKL group was subjected to intraperitoneal injections of LSKL twice weekly for four weeks. To measure intracavernous pressure (ICP), a 25-gauge needle connected to a PE tube containing heparin was inserted into the corpus cavernosum (CC). Additionally, a needle was inserted into the carotid artery to measure mean arterial pressure (MAP). Sirius red staining and Masson trichrome staining were utilized to assess CC fibrosis. Moreover, high glucose (HG)-induced CC smooth muscle cells (CCSMCs) and CC fibroblasts (CCFs) were treated with or without LSKL. Western blotting and immunofluorescence were utilized to assess the phosphorylation and expression of related proteins.

resultsCompared with those in the control group, the ratio of the maximum ICP to the MAP markedly decreased in the DMED group, as did the ratio of smooth muscle to collagen and the ratio of collagen I to collagen III. These ratios were greater in the DMED+LSKL group than in the DMED group. TSP1 was highly expressed in the CC of DMED rats.

conclusionsTSP1 expression is increased in the CC of DMED rats. HG-induced TSP1 secretion via autocrine signaling from CCSMCs and/or paracrine signaling from CCFs to accelerate penile fibrosis. LSKL, an antagonist of TSP1, could improve erectile dysfunction by inhibiting the TGF-β/SMAD pathway.

Indexed as

Diabetes mellitusErectile dysfunctionFibrosisTransforming growth factor beta1

Identifiers

PMID39344111
PMCPMC12257313

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.