Comparative histological, immunohistochemical, and biochemical effects of three orally administered fluoroquinolones

Turan Yaman1, Fatih Donmez2, Abdulahad Dogan2

  • 1Department of Pathology, Faculty of Veterinary Medicine, Van Yuzuncu Yil University, Van, Turkey.

PubMed

Insights

Fluoroquinolone antibiotics can cause testicular damage and inflammation in male rats. This study investigated the effects of ciprofloxacin, levofloxacin, and moxifloxacin on rat testes, revealing potential male reproductive toxicity.

Area of Science:

  • Pharmacology
  • Toxicology
  • Reproductive Biology

Background:

  • Fluoroquinolones (FQs) are broad-spectrum antibiotics with widespread use in human and veterinary medicine.
  • Concerns exist regarding the potential reproductive toxicity of FQs, necessitating further investigation.

Purpose of the Study:

  • To assess the histological, immunohistochemical, and biochemical impacts of ciprofloxacin (CIP), levofloxacin (LVX), and moxifloxacin (MXF) on rat testicular tissue.
  • To evaluate the time-dependent effects of these FQ derivatives on male reproductive health.

Main Methods:

  • Seventy-two male Wistar albino rats were divided into control and treatment groups (CIP, LVX, MXF).
  • Oral administration of FQs was followed by testicular tissue collection at three time points (Days 1, 7, 14).
  • Histopathology (H&E), immunohistochemistry (COX-2), and biochemical assays (MDA, ADA, AChE) were performed.

Main Results:

  • Fluoroquinolone exposure induced varying degrees of testicular degeneration and increased COX-2 expression.
  • Moxifloxacin (MXF) showed a time-dependent decrease in malondyaldehyde (MDA) levels.
  • Adenosine deaminase (ADA) activity increased with CIP and LVX, while acetylcholine esterase (AChE) levels rose with LVX and MXF.

Conclusions:

  • Fluoroquinolone derivatives exhibit time-dependent degenerative and inflammatory effects on testicular tissue.
  • These findings indicate a potential risk of male reproductive toxicity associated with FQ use.
  • Further research is warranted to elucidate the mechanisms underlying FQ-induced reproductive toxicity.