Evidence map›Paper›PMID 32336289›Full record

ArticleBMC complementary medicine and therapies2020

Neuroprotective effect of diosgenin in a mouse model of diabetic peripheral neuropathy involves the Nrf2/HO-1 pathway.

Jinhong Leng, Xiaohua Li, He Tian, Chang Liu, Yining Guo, Su Zhang, Yang Chu, Jian Li, Ying Wang, Ling Zhang

Open access · goldAbstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Diosgenin ameliorates silica-induced tuberculosis in rats.Animal models and experimental medicine · 2025
    Article
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  7. Review
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  19. Article
  20. Effect of Noni on Memory Impairment Induced by Hydrocortisone in Mice.Evidence-based complementary and alternative medicine : eCAM · 2022
    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

10 authors at 3 institutions in 1 country.

Jinhong LengDepartment of Endocrinology, Affiliated Hospital of Liaoning University of Traditional Chinese Medicine, Shenyang, 110032, Liaoning, China.
Xiaohua LiDepartment of Traditional Chinese Medicine Clinical Endocrinology, Liaoning University of Traditional Chinese Medicine Graduate School, Shenyang, 110847, Liaoning, China.
He TianDepartment of Histology and Embryology, School of Basic Medicine, Jinzhou Medical University, Jinzhou, 121000, Liaoning, China. jytianhe@foxmail.com.
Chang LiuDepartment of Endocrinology, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, 121000, Liaoning, China. liuchang1971mei@163.com.
Yining GuoDepartment of Traditional Chinese Medicine Clinical Endocrinology, Liaoning University of Traditional Chinese Medicine Graduate School, Shenyang, 110847, Liaoning, China.
Su ZhangDepartment of Traditional Chinese Medicine Clinical Endocrinology, Liaoning University of Traditional Chinese Medicine Graduate School, Shenyang, 110847, Liaoning, China.
Yang ChuDepartment of Traditional Chinese Medicine Clinical Endocrinology, Liaoning University of Traditional Chinese Medicine Graduate School, Shenyang, 110847, Liaoning, China.
Jian LiDepartment of Traditional Chinese Medicine Clinical Endocrinology, Liaoning University of Traditional Chinese Medicine Graduate School, Shenyang, 110847, Liaoning, China.
Ying WangDepartment of Traditional Chinese Medicine Clinical Endocrinology, Liaoning University of Traditional Chinese Medicine Graduate School, Shenyang, 110847, Liaoning, China.
Ling ZhangDepartment of Traditional Chinese Medicine Clinical Endocrinology, Liaoning University of Traditional Chinese Medicine Graduate School, Shenyang, 110847, Liaoning, China.
Liaoning University of Traditional Chinese Medicine · CNJinzhou Medical University · CNAffiliated Hospital of Liaoning University of Traditional Chinese Medicine · CN

Funding

Natural Science Foundation of Liaoning Province 20180530030Natural Science Foundation of Liaoning Province 20180550649Shenyang Science and Technology Bureau 18-013-0-09
6 · The paper itself

Abstract

backgroundDiabetic peripheral neuropathy (DPN) is one of the most common chronic complications of diabetes. Diosgenin is a natural steroidal saponin with a variety of beneficial effects, including antidiabetic effects, and is a raw material for the synthesis of carrier hormones. In our study, we aimed to assess the antioxidant effects of diosgenin in diabetic mice.

methodsMale C57 mice were fed a high-fat diet for 8 weeks and intraperitoneally injected with streptozotocin (STZ) at a dose of 100 mg/kg for 2 consecutive days. Eligible mice were divided into the normal control group (CON), diabetic group (DM), low-dose diosgenin (50 mg/kg) group (DIO50) and high-dose diosgenin (100 mg/kg) group (DIO100). Treatment was started 6 weeks after the induction of diabetes by STZ and continued for 8 weeks. Blood sugar and body weight were monitored dynamically. The behavioural effects of diosgenin were detected by a hot tail immersion test and paw tactile responses. HE staining was used to evaluate edema and degeneration of the sciatic nerve. The levels of SOD, MDA and GPx were tested according to the instructions of the respective kits. The levels of Nrf2, HO-1 and NQO1 were detected by immunofluorescence and Western blotting. Statistical analysis was performed using SPSS, and P < 0.05 was considered statistically significant.

resultsDiosgenin decreased the blood glucose levels and increased the body weight of diabetic mice. There was a significant increase in the tail withdrawal latency of diabetic animals, and mechanical hyperalgesia was significantly alleviated after diosgenin treatment. Histopathological micrographs of HE-stained sciatic nerves showed improvement after diosgenin treatment. Diosgenin attenuated the level of MDA but increased the activities of SOD and GPx. Diosgenin increased the expression of Nrf2, HO-1 and NQO1.

conclusionsOur results demonstrate that diosgenin can ameliorate behavioural and morphological changes in DPN by reducing oxidative stress. The Nrf2/HO-1 signalling pathway was involved in its neuroprotective effects.

Indexed as

AnimalsDiabetes Mellitus, ExperimentalDiabetic NeuropathiesDiet, High-FatDiosgeninDisease Models, AnimalHeme Oxygenase-1MaleMembrane ProteinsMiceNeuroprotective AgentsNF-E2-Related Factor 2StreptozocinDiosgeninHeme Oxygenase-1Hmox1 protein, mouseMembrane ProteinsNeuroprotective AgentsNfe2l2 protein, mouseNF-E2-Related Factor 2StreptozocinDiabetic peripheral neuropathyDiosgeninHO-1Nrf2Oxidative stress

Identifiers

PMID32336289
PMCPMC7184706
OpenAlexW3019539493

What OpenQuestion holds

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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.