Evidence map›Paper›PMID 34846706›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2022

Improvement of Astragalin on Spermatogenesis in Oligoasthenozoospermia Mouse Induced by Cyclophosphamide.

Qigang Fan, Zhongying Zhao, Qing Meng, Ruifeng He, Hongli Li, Meigui Zhang, Pu Gao, Xinlong Li, Yi Li, Qinying Zhu and 3 more

Abstract read
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In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
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

11 citing papers in PubMed, 20 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Qigang FanThe First Clinical Medical College of Lanzhou University, Lanzhou, China.
Zhongying ZhaoThe First Clinical Medical College of Lanzhou University, Lanzhou, China.
Qing MengSchool of Life Sciences, Lanzhou University, Lanzhou, China.
Ruifeng HeThe First Clinical Medical College of Lanzhou University, Lanzhou, China.
Hongli LiDepartment of Obstetrics and Gynecology, Key Laboratory for Gynecologic Oncology Gansu Province, The First Hospital of Lanzhou University, Lanzhou, China.
Meigui ZhangThe First Clinical Medical College of Lanzhou University, Lanzhou, China.
Pu GaoSecond Clinical Medical College of Lanzhou University, Lanzhou, China.
Xinlong LiSecond Clinical Medical College of Lanzhou University, Lanzhou, China.
Yi LiThe First Clinical Medical College of Lanzhou University, Lanzhou, China.
Qinying ZhuThe First Clinical Medical College of Lanzhou University, Lanzhou, China.
Fengqin ShenSecond Clinical Medical College of Lanzhou University, Lanzhou, China.
Lihui ZhaoDepartment of Obstetrics and Gynecology, Key Laboratory for Gynecologic Oncology Gansu Province, The First Hospital of Lanzhou University, Lanzhou, China.
Xiaolei LiangDepartment of Obstetrics and Gynecology, Key Laboratory for Gynecologic Oncology Gansu Province, The First Hospital of Lanzhou University, Lanzhou, China. liangxl07@lzu.edu.cn.
First Hospital of Lanzhou University · CNLanzhou University · CNLanzhou University Second Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

More than 40% of infertile men are diagnosed with oligoasthenozoospermia and the incidence is still rising, but the effective treatments are not been found until now. Astragalin, one of the main active ingredients in traditional Chinese medicine, may be effective in the treatment of oligoasthenozoospermia. This study investigated the pharmacological effects of astragalin for treatment of oligoasthenozoospermia in male mice, induced by cyclophosphamide (CTX). Male mice were intraperitoneally injected by CTX (50 mg/kg), and astragalin (30 mg/kg) was given via oral gavage once daily. RNA-seq analysis highlighted astragalin upregulated gene expression of anti-apoptosis (AKT1and BCL2-XL), cell proliferation (ETV1, MAPKAPK2, and RPS6KA5) and synthesis of testosterone (STAR, CYP11A1, and PRKACB), but downregulated gene expression of cell apoptosis (BAD, BCL-2, CASPASE9, and CASPASE3) in mouse testis. Astragalin also significantly reversed the reduction in body weight, reproductive organs index, and sperm parameters (sperm concentration, viability, and motility) induced by CTX, and restored testicular abnormal histopathologic morphology induced by CTX. Furthermore, astragalin dramatically rescued the gene expression related to spermatogenesis (AKT1, BCL-2, CASPASE9, CASPASE3, MAPKAPK2, RPS6KA5, STAR, and PRKACB), and increased the level of testosterone by improving related proteins (STAR, CYP11A1, PRKACB) for oligoasthenozoospermia induced by CTX. In conclusion, astragalin may be a potential beneficial agent for oligoasthenozoospermia by increasing the testosterone levels in testis.

Indexed as

KaempferolsOligospermiaSpermatogenesisAnimalsCyclophosphamideMaleMiceSpermatozoaSperm MotilityTestisTestosteroneastragalinCyclophosphamideKaempferolsTestosteroneAstragalinHormoneOligoasthenozoospermiaSpermatogenesis

Identifiers

PMID34846706
OpenAlexW3215996865

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.