AN ASSESSMENT OF POSSIBLE PROTECTIVE ROLES OF MORPHINE AND NALOXONE ON THE ACUTE TOXICITY OF T-2 TOXIN

• Published in: Cereal research communications Vol. 25; no. 3; pp. 457 - 458
• Main Authors: YAZDANPANAH, H., RASEKH, H. R., ROSHANZAMIR, F., SHAFAGHI, B., ABBASI, KH, NADERI, N.
• Format: Journal Article
• Language: English
• Published: Cereal Research Institute 01-01-1997
• Subjects: Acute toxicity; Health care administration; Human resources; Morphine; Mortality; Mycotoxins; Opioid analgesics; Pharmacology; Poster presentations; Toxicity; Toxins
• ISSN: 0133-3720; 1788-9170
• DOI: 10.1007/bf03543754

The efficacy of naloxone and morphine on acute toxicity of T-2 toxin, a potent cytotoxic trichothecene mycotoxin, was investigated. In this study, mice received naloxone (4 or 8 mg/kg, sc) or morphine (5 or 15 mg/kg, sc) 24, 18, 1 hr before and 6 hr after ip injection of 2 or 1.8 mg/kg of T-2 toxin, respectively. In addition, naloxone (8 mg/kg, sc) were administered at 13, 7, 1 hr before, and 5 hr after T-2 toxin administration (1.8 mg/kg, ip). The acute lethal toxicity and change in body and organ weights (including liver, spleen, and kidneys) were evaluated. The acute lethal toxicity of T-2 toxin was reduced by administration of the first regimen of naloxone (8 mg/kg, sc). It also caused a protective effect against T-2 toxin-induced weight changes. On the other hand, morphine increased T-2 toxin-induced lethality (although not statistically significant). It could be concluded that opioid agonists may exacerbate the lethal toxicity of T-2 toxin-induced shock and opioid antagonists such as naloxone could antagonize this shock.