Research Trends and Hotspots Analysis Related to the Effects of Xenobiotics on Glucose Metabolism in Male Testes

Int J Environ Res Public Health. 2018 Jul 26;15(8):1590. doi: 10.3390/ijerph15081590.

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.

Keywords: CiteSpace; bibliometrics; glucose metabolism; testes; xenobiotics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bibliometrics*
  • Biomedical Research / trends
  • Databases, Factual
  • Glucose / metabolism*
  • Humans
  • L-Lactate Dehydrogenase / metabolism
  • Male
  • Oxidative Stress / physiology
  • PubMed
  • Publications
  • Research*
  • Sertoli Cells / metabolism
  • Testis / metabolism*
  • Xenobiotics / pharmacology*

Substances

  • Xenobiotics
  • L-Lactate Dehydrogenase
  • Glucose