Evidence map›Paper›PMID 40762464›Full record

ArticleAsian journal of andrology2026

Ginsenoside Rb1 mitigates diabetes-induced erectile dysfunction in rats by reducing oxidative stress and modulating the PI3K/AKT/eNOS pathway.

Zong-Hai Liu, Wei-Bo Chen, Jian-Zheng Li, Xue-Sheng Wang, Lei Liu, Han-Wen Liu, Gong-Zhen Chen, Chao Pan, Ming-Zhen Yuan

Abstract read
In one paragraph

Article in Asian journal of andrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
  2. Review
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

9 authors.

Zong-Hai LiuShandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan 250021, China.
Wei-Bo ChenShandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan 250021, China.
Jian-Zheng LiShandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan 250021, China.
Xue-Sheng WangShandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan 250021, China.
Lei LiuDepartment of Urology, The Second Hospital of Shandong University, Jinan 250013, China.
Han-Wen LiuDepartment of Urology, The Second Hospital of Shandong University, Jinan 250013, China.
Gong-Zhen ChenShandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan 250021, China.
Chao PanShandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan 250021, China.
Ming-Zhen YuanShandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan 250021, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erectile dysfunction is a complex and prevalent complication of diabetes, and effective treatments are lacking. Oxidative stress, fibrosis, and apoptosis are closely associated with the development of diabetes mellitus-related erectile dysfunction (DMED). Notably, ginsenoside Rb1 (Rb1) exerts antioxidant effects and displays promise in the treatment of DMED. This study evaluated the therapeutic efficacy of Rb1 in a rodent streptozotocin-induced DMED model. Thirty-two rats were randomly assigned to three groups: control group, DMED group, and DMED + Rb1 group. DMED was induced in male rats via an intraperitoneal injection of streptozotocin. After 8 weeks of Rb1 gavage, erectile function was assessed by the electrical stimulation of the cavernous nerve. In addition, western blot, quantitative real-time polymerase chain reaction, enzyme-linked immunosorbent assay, immunofluorescence, terminal deoxynucleotidyl transferase (TdT) dUTP nick-end labeling (TUNEL) staining, and Masson's trichrome staining were performed to verify the relevant factors and protein expression. Rb1 effectively improved the erectile function of the corpus cavernosum, decreased collagen content, and increased smooth muscle content in rats with diabetes. Rb1 decreased the levels of the pro-inflammatory factors (interleukin [IL]-6, tumor necrosis factor alpha [TNF-α], and IL-1β), and increased the levels of the anti-inflammatory factors (IL-10 and IL-4). Moreover, the activities of superoxide dismutase and catalase and levels of nitric oxide (NO) were increased, whereas malondialdehyde activity was decreased. Additionally, Rb1 activated the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT)/endothelial nitric oxide synthase (eNOS) signaling pathway and inhibited cell apoptosis. Rb1 can improve erectile function in rats with DMED by increasing the activity of the PI3K/AKT/eNOS pathway, reducing oxidative stress, inhibiting inflammation and apoptosis, and alleviating corpus cavernosum fibrosis.

Indexed as

Diabetes ComplicationsDiabetes Mellitus, ExperimentalErectile DysfunctionGinsenosidesOxidative StressAnimalsApoptosisMaleNitric Oxide Synthase Type IIIPenisPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRatsRats, Sprague-DawleySignal Transductionginsenoside Rb1GinsenosidesNitric Oxide Synthase Type IIINos3 protein, ratPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktdiabetes mellituserectile dysfunctionginsenoside Rb1oxidative stressPI3K/AKT/eNOS

Identifiers

PMID40762464
PMCPMC12912748

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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.