Curcumin-Loaded Iron Particle Improvement of Spermatogenesis in Azoospermic Mouse Induced by Long-Term Scrotal Hyperthermia

Reprod Sci. 2021 Feb;28(2):371-380. doi: 10.1007/s43032-020-00288-2. Epub 2020 Aug 11.

Abstract

Spermatogenesis process is sensitive to heat stress because the testicular temperature is 2 to 4 °C lower than the core body temperature. The current study aimed to investigate the effects of iron oxide nanoparticles containing curcumin on spermatogenesis in mice induced by long-term scrotal hyperthermia. In this experimental study, 18 mice were equally divided into the following three groups: control, scrotal hyperthermia, and scrotal hyperthermia + curcumin-loaded iron particles (NPs) (240 μL) (mice were treated for 20 days). Hyperthermia was induced by exposure to the temperature of 43 °C for 20 min every other day for 5 weeks. Afterward, the animals were euthanized; sperm samples were collected for sperm parameters analysis, and testis samples were taken for histopathology experiments, evaluation of serum testosterone level, and RNA extraction in order to examine the expression of c-kit, STRA8 and PCNA genes. Our study showed that curcumin-loaded iron particles could notably increase the volume of testis, length of seminiferous tubules, sperm parameters, and stereological parameters (i.e., spermatogonia, primary spermatocyte, round spermatid, and Leydig cells) thereby increasing serum testosterone level; in addition, TUNEL-positive cells showed a significant decrease in curcumin-loaded iron particle group. Thus, based on the obtained results, the expression of c-kit, STRA8, and PCNA genes was significantly increased in treatment groups by curcumin-loaded iron particles compared with scrotal hyperthermia-induced mice. In conclusion, curcumin-loaded iron particles can be considered an alternative treatment for improving the spermatogenesis process in scrotal hyperthermia-induced mice.

Keywords: Curcumin-loaded iron particles; Long-term scrotal hyperthermia; Spermatogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Animals
  • Azoospermia / blood
  • Azoospermia / drug therapy*
  • Azoospermia / etiology
  • Azoospermia / pathology
  • Biomarkers / blood
  • Curcumin / chemistry
  • Curcumin / pharmacology*
  • Disease Models, Animal
  • Drug Carriers*
  • Drug Compounding
  • Fertility Agents, Male / chemistry
  • Fertility Agents, Male / pharmacology*
  • Hyperthermia, Induced
  • Magnetic Iron Oxide Nanoparticles / chemistry*
  • Male
  • Mice
  • Proliferating Cell Nuclear Antigen / genetics
  • Proliferating Cell Nuclear Antigen / metabolism
  • Proto-Oncogene Proteins c-kit / genetics
  • Proto-Oncogene Proteins c-kit / metabolism
  • Spermatogenesis / drug effects*
  • Spermatozoa / drug effects*
  • Spermatozoa / metabolism
  • Spermatozoa / pathology
  • Testis / drug effects*
  • Testis / metabolism
  • Testis / pathology
  • Testis / physiopathology
  • Testosterone / blood
  • Time Factors

Substances

  • Adaptor Proteins, Signal Transducing
  • Biomarkers
  • Drug Carriers
  • Fertility Agents, Male
  • Proliferating Cell Nuclear Antigen
  • Stra8 protein, mouse
  • Testosterone
  • Proto-Oncogene Proteins c-kit
  • Curcumin