| Literature DB >> 30050010 |
Yongsheng Fan1, Guangxia Yu2, Jun Yu3, Jiantao Sun4, Yu Wu5, Xue Zhao6, Yu Meng7, Zhangdong He8, Chunhong Wang9.
Abstract
This study aimed to integrate and analyze the existing studies and to explore research trends and hotspots related to the effects of xenobiotics on glucose metabolism in male testes. All articles were retrieved from the PubMed database, from an inception date up to 10 June 2017. CiteSpace software (version 5.1.R8 SE) was used for the co-word cluster analysis. A total of 165 eligible publications were included in this study. In 1949⁻1959, only two articles were published. After 1960, the number of articles increased steadily. These articles were published in 97 journals, in particular, in the Indian Journal of Experimental Biology (11 articles, 6.7%). Most of the authors (87.0%) only published one article. Only a few established research teams, mostly from the USA, worked consistently in this field. The main xenobiotics that had been studied were medicine and common environmental pollutants, e.g., gossypol, cadmium, di-n-butyl phthalate, and alpha-chlorohydrin. The hotspot keywords were Sertoli cell, lactate dehydrogenase, 6-phosphate dehydrogenase, oxidative stress, and glucose metabolism. The focus of research had been changed overtime. This is the first bibliometric study between xenobiotics and glucose metabolism in the male testes. The findings suggest that environmental pollutants have become a huge concern, and related research should be strengthened.Entities:
Keywords: CiteSpace; bibliometrics; glucose metabolism; testes; xenobiotics
Mesh:
Substances:
Year: 2018 PMID: 30050010 PMCID: PMC6121400 DOI: 10.3390/ijerph15081590
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390
Figure 1Flow diagram of study selection based on PRISMA 2009 guidelines [10] (PRISMA is an evidence-based minimum set of items for reporting in systematic reviews and meta-analyses).
Figure 2The distribution of 165 included articles: (a) by publication year; (b) by continents and year.
The 5 most productive countries for publications of effects of xenobiotics on glucose metabolism in testes.
| Rank | Country | Continent | Articles | Percent (%) |
|---|---|---|---|---|
| 1 | India | Asia | 54 | 32.7 |
| 2 | USA | America | 33 | 20.0 |
| 3 | China | Asia | 11 | 6.7 |
| 4 | Egypt | Africa | 8 | 4.9 |
| 5 | Portugal | Europe | 7 | 4.2 |
The 5 most productive authors for publications of effects of xenobiotics on glucose metabolism in testes.
| Author | Country | Publications | Percent (%) |
|---|---|---|---|
| Satya P. Srivastava | India | 5 | 3.03 |
| Mannfred A. Hollinger | USA | 4 | 2.42 |
| Syed Husain | USA | 4 | 2.42 |
| Peter F. Hall | USA | 3 | 1.82 |
| Pedro F. Oliveira | Portugal | 3 | 1.82 |
Figure 3The distribution of xenobiotics studied related to glucose metabolism in testes: (a) by publication year; (b) types.
Figure 4A network of co-words of 165 articles.
The top 7 co-word clusters with high frequency and silhouette in articles examining effects of xenobiotics on glucose metabolism in testes.
| Frequency | Silhouette | ||||
|---|---|---|---|---|---|
| Rank | Frequency | Clusters | Rank | Silhouette | Clusters |
| 1 | 25 | Sertoli cell | 1 | 0.84 | Sertoli cell |
| 2 | 17 | lactate dehydrogenase | 2 | 0.46 | lactate dehydrogenase |
| 3 | 14 | 6-phosphate dehydrogenase | 3 | 0.37 | glucose metabolism |
| 4 | 13 | oxidative stress | 4 | 0.28 | 6-phosphate dehydrogenase |
| 5 | 12 | rat testis | 5 | 0.24 | oxidative stress |
| 6 | 10 | male rat | 6 | 0.24 | γ-glutamyl transpeptidase |
| 7 | 8 | glucose metabolism | 7 | 0.20 | germ cell |
Figure 5Timeline view for co-words analysis.
Figure 6The main regulatory pathways induced by xenobiotics. Malondialdehyde (MDA), Superoxide radical (O2−), Hydrogen peroxide (H2O2), Reactive oxygen species (ROS), Peroxisome proliferator-activated receptor-gamma (PPAR-γ), Superoxide dismutase (SOD), Catalase (CAT), Glutathione peroxidase (GPx), Glutathione-S-transferase (GST), Glutathione reductase (GR), Reduced glutathione (GSH), Succinate dehydrogenase (SDH), Malate dehydrogenase (MDH), Isocitrate dehydrogenase (ICDH), Phosphofructokinase (PFK), Lactate dehydrogenase (LDH).