Acute oral toxicity and antioxidant studies of an amine-based diselenide

• Published in: BMC complementary and alternative medicine Vol. 19; no. 1; p. 80
• Main Authors: Ibrahim, Mohammad, Muhammad, Niaz, Ibrahim, Musadiq, Khan, Muhammad Idrees, Shah, Muhammad Ishaq Ali, Said, Muhammad, Khan, Waliullah, Kamdem, Jean Paul, Rocha, Joao Batista Teixeira
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 03-04-2019; BioMed Central; BMC
• Subjects: Acids; Acute toxicity; Amines; Animals; Antioxidant; Antioxidants; Antioxidants (Nutrients); Ascorbic acid; Biocompatibility; Biological activity; Body weight; Canola oil; Catalase; Drug dosages; Enzymes; Free radicals; Iron; Laboratory rats; LD50; Lethal dose; Lipid peroxidation; Lipids; Liver; Mice; Oral administration; Organic chlorine compounds; Organoselenium; Organoselenium compounds; Oxidative stress; Parameters; Peroxidation; Pharmacological research; Pharmacology; Proteins; Selenium; Superoxide dismutase; Superoxides; Thiobarbituric acid; Thiols; Toxicity; Vitamin C; Vitamins; Brazil; LD50; Lipid peroxidation; Antioxidant; Organoselenium; Toxicity; Vitamin C
• ISSN: 1472-6882; 1472-6882
• DOI: 10.1186/s12906-019-2489-5

Organochalcogen compounds have attracted the interest of a multitude of studies for their promising Pharmacological and biological activities. The antioxidant activity and acute toxicity of an organoselenium compound, 1-(2-(2-(2-(1-aminoethyl)phenyl)diselanyl)phenyl)ethanamine (APDP) was determined in mice.
Mice were randomly divided into four groups, with each group comprising of seven animals. Canola oil (1ml/kg of body weight) was administered to 1st group, while 2nd, 3rd & 4th groups were administered with 10 mg/kg, 30 mg/kg & 350 mg/kg of APDP respectively. APDP was administered by Intragastric gavage as a single oral dose.
The APDP oral administration was found to be safe up to 350 mg/kg of body weight and no deaths of animals were recorded. The lethal dose 50 (LD
) for APDP was determined at 72 h and was estimated to be > 350 mg/kg. After acute treatment, all mice were sacrificed by decapitation to determine the antioxidant enzymes and lipid peroxidation values for the treated mice liver. No fluctuation in lipid peroxidation, vitamin C and non protein thiol (NPSH) levels was observed due to the administration of APDP. hepatic α-ALA-D activity, catalase (CAT), superoxide dismutase (SOD) and the biochemical parameters were evaluated. Experimental observation demonstrated that APDP protected Fe(II) induced thiobarbituric acid reactive substances (TBARS) production in liver homogenate significantly (p < 0.05). The administration of APDP (an amine-based diselenide) both in vitro and in vivo clearly demonstrated that this potential compound has no acute toxicity towards mice among all the tested parameter.
On the basis of experimental results, it is concluded that APDP is a potential candidate as an antioxidant compound for studying pharmacological properties.