Evaluation of the non-clinical toxicity of an antiparasitic agent: diminazene aceturate

Abstract

The diminazene aceturate (C₁₄H₁₅N₇.2C₄H₇NO₃) is a chemotherapeutic agent with more than six decades of use, however more studies regarding its toxicity still need to be performed. Thus, the present study determined the acute toxicity (14 days) of diminazene acetate (DIZE) in male and female swiss mice by changes in body mass, food consumption, biochemical and hematological parameters, locomotor activity and motor coordination. DIZE was administered at a single dose (1000 and 2000 mg/kg) orally. In addition, in vitro antioxidant capacity, hemolytic activity, toxicity in Artemia salina and in silico evaluation were also performed. The results obtained include several signs of toxicity (hypoactivity, loss of the straightening reflex and tachycardia), reduction of behavioral activity (locomotor activity and motor coordination) and significant changes (p < 0.05) in biochemical and hematological parameters. According to the in silico study, the DIZE can be classified based on the mean lethal dose (LD₅₀) in category 4 (300 mg/kg < LD₅₀ ≤ 2000 mg/kg, ProTox-II) or 3 (50 mg/kg < LD₅₀ ≤ 300 mg/kg, AdmetSAR 1.0). Additionally, DIZE (30.3–969.9 nM) was not toxic to A. salina in the first 48 hours of treatment and was not cytotoxic to rat red blood cells after induced hemolysis. In vitro results indicated low antioxidant capacity against DPPH^• and ABTS^•+ radicals. Therefore, DIZE induces several adverse effects with influence on the central nervous system, changes in hematological and biochemical parameters and even mortality at the highest dose. However, absence of toxicity was observed in A. salina and rats red blood cells.

Keywords:

• Artemia salina
• antioxidant capacity
• acute toxicity
• diminazene aceturate
• toxicity in silico

Disclosure statement

The authors declare that there is no conflict of interest.