Effects of two kinds of fishery drugs on the expressions of GAD and GABA-T mRNA in crucian carp (Carassius auratus gibelio)

Fish Physiol Biochem. 2020 Dec;46(6):1965-1973. doi: 10.1007/s10695-020-00847-z. Epub 2020 Jul 15.

Abstract

The objective of this study was to investigate the effects of difloxacin (DIF) and avermectin (AVM) on glutamate decarboxylase (GAD) and GABA-transaminase (GABA-T) in different tissues of crucian carp (Carassius auratus gibelio). After the treatments of DIF and AVM, the mRNA expressions of GAD and GABA-T in different tissues were detected by quantitative real-time PCR (qPCR). The results showed that the mRNA expressions of GAD65, GAD67, and GABA-T in the telencephalon (Tel), mesencephalon (Mes), cerebella (Cer), and medulla oblongata (Med) were downregulated significantly with the safe dose (SD, 20 mg/kg) of DIF (P < 0.05 or P < 0.01). While the expressions of GAD65 and GAD67 in the kidney at 12 h had strikingly upregulated to 13.81 ± 1.06** and 150.67 ± 12.85** times. Treated with the lethal dose of 50% (LD50, 2840 mg/kg b. W.) of DIF, the mRNA expressions of GAD65, GAD67, and GABA-T in all tissues were increased significantly (P < 0.01). The results of AVM group showed that the mRNA expressions of GAD65, GAD67, and GABA-T both in the central and peripheral tissues were all remarkably downregulated at the safe concentration (SC, 0.0039 mg/L) and the lethal concentration of 50% (LC50, 0.039 mg/L), except for the mRNA inhibitions of GAD65, GAD67, and GABA-T in the muscle at 2 h which sharply downregulated to 0.20 ± 0.02ΔΔ × 10-2, 0.57 ± 0.06ΔΔ × 10-1 and 0.44 ± 0.02ΔΔ × 10-1, respectively (P < 0.01).

Keywords: Avermectin; Difloxacin; GABA-transaminase; Gamma-aminobutyric acid; Glutamate decarboxylase.

Publication types

  • Randomized Controlled Trial, Veterinary

MeSH terms

  • 4-Aminobutyrate Transaminase / genetics*
  • Animals
  • Anti-Bacterial Agents / pharmacology*
  • Antiprotozoal Agents / pharmacology*
  • Brain / drug effects
  • Brain / metabolism
  • Carps / genetics*
  • Ciprofloxacin / analogs & derivatives*
  • Ciprofloxacin / pharmacology
  • Fisheries
  • Glutamate Decarboxylase / genetics*
  • Ivermectin / analogs & derivatives*
  • Ivermectin / pharmacology
  • Kidney / drug effects
  • Kidney / metabolism
  • Liver / drug effects
  • Liver / metabolism
  • Muscles / drug effects
  • Muscles / metabolism
  • RNA, Messenger / metabolism

Substances

  • Anti-Bacterial Agents
  • Antiprotozoal Agents
  • RNA, Messenger
  • Ciprofloxacin
  • difloxacin
  • Ivermectin
  • avermectin
  • 4-Aminobutyrate Transaminase
  • Glutamate Decarboxylase