<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(10)</volume><submitter>Zhang MH</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>This study observes changes in levels of seminal nitric oxide (NO), nitric oxide synthase (NOS), macrophage migration inhibitory factor (MIF), sperm DNA integrity, chromatin condensation and Caspase-3in adult healthy men after scrotal heat stress (SHS).&lt;h4>Methods&lt;/h4>Exposure of the scrotum of 25 healthy male volunteers locally at 40-43°C SHS belt warming 40 min each day for successive 2 d per week. The course of SHS was continuously 3 months. Routine semen analysis, hypo-osmotic swelling (HOS) test, Aniline blue (AB) staining, HOS/AB and terminal deoxynucleotidyl transferase-mediated d UDP nick-end labeling (TUNEL) were carried out before, during and after SHS. Seminal NO and NOS contents were determined by nitrate reduction method. The activated Caspase-3 levels of sp</pubmed_abstract><journal>PloS one</journal><pagination>e0141320</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4626044</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Changes in Levels of Seminal Nitric Oxide Synthase, Macrophage Migration Inhibitory Factor, Sperm DNA Integrity and Caspase-3 in Fertile Men after Scrotal Heat Stress.</pubmed_title><pmcid>PMC4626044</pmcid><pubmed_authors>Qiu Y</pubmed_authors><pubmed_authors>Zhang AD</pubmed_authors><pubmed_authors>Wang LG</pubmed_authors><pubmed_authors>Zhang MH</pubmed_authors><pubmed_authors>Shi ZD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Changes in Levels of Seminal Nitric Oxide Synthase, Macrophage Migration Inhibitory Factor, Sperm DNA Integrity and Caspase-3 in Fertile Men after Scrotal Heat Stress.</name><description>&lt;h4>Background&lt;/h4>This study observes changes in levels of seminal nitric oxide (NO), nitric oxide synthase (NOS), macrophage migration inhibitory factor (MIF), sperm DNA integrity, chromatin condensation and Caspase-3in adult healthy men after scrotal heat stress (SHS).&lt;h4>Methods&lt;/h4>Exposure of the scrotum of 25 healthy male volunteers locally at 40-43°C SHS belt warming 40 min each day for successive 2 d per week. The course of SHS was continuously 3 months. Routine semen analysis, hypo-osmotic swelling (HOS) test, Aniline blue (AB) staining, HOS/AB and terminal deoxynucleotidyl transferase-mediated d UDP nick-end labeling (TUNEL) were carried out before, during and after SHS. Seminal NO and NOS contents were determined by nitrate reduction method. The activated Caspase-3 levels of sp</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015</publication><modification>2025-04-19T15:27:55.525Z</modification><creation>2019-03-26T23:28:04Z</creation></dates><accession>S-EPMC4626044</accession><cross_references><pubmed>26512992</pubmed><doi>10.1371/journal.pone.0141320</doi></cross_references></HashMap>