Effect of acute exposure of triazophos on oxidative stress and histopathological alterations in liver, kidney and brain of Wistar rats.

Acute dose of organophosphorus pesticide Triazophos (O,O-diethyl O-1-phenyl-1H-1,2,4-triazol-3-yl phosphorothioate; Tz) administered orally affects oxidative stress parameters and the histo-architecture of liver, kidney and brain tissues. The results indicate a dose dependent induction of oxidative stress as evident by increased malondialdehyde level and decreased antioxidant defense including glutathione and superoxide dismutase activity in rat liver, kidney and brain. AChE activity was found significantly decreased in the Tz treated groups as compared to the vehicle control (DMSO) group. Histopathological examination of liver, kidney and brain in Tz treated rats revealed medullary congestion and hydropic degeneration of hepatocytes in liver and medullary congestion in kidney. However, no significant histopathological changes were observed in brain tissues.

Induction of oxidative stress and histopathological changes by sub-chronic doses of triazophos.

The effect of triazophos (O, O-diethyl O-1-phenyl-1 H-1, 2, 4-triazol-3-yl phosphorothioate), a widely used insecticide was studied on the induction of oxidative stress and histological alterations at sub-chronic doses in male albino rats. Oral administration of triazophos at concentrations of 1.64, 3.2 and 8.2 mg/kg body wt for 30 days produced dose as well as time-dependent increase in the lipid peroxidation (determined by malondialdehyde levels) and glutathione-S-transferase (GST) activity in serum with a concomitant decrease in ferric reducing ability of plasma (FRAP) and blood glutathione (GSH) content. Histopathological examination of liver of triazophos-treated rats showed significant and progressive degenerative changes as compared to control, which could be due to induction of oxidative stress. However, no significant histopathological changes were observed in spleen, kidney and brain at either dose of triazophos with respect to control. These results indicated that oral administration of triazophos was associated with enhanced lipid peroxidation and compromised antioxidant defence in rats in dose and time-dependent manner. Thus the present study demonstrated for the first time the role of oxidative stress as the important mechanism involved in the stimulation of hepatic histo-architectural alterations at sub-chronic doses of triazophos in rats.

Toxic effects of five insecticides and their mixture on male albino rats

Five insecticides namely; abamectin, carbosulfan, fenpropathrin, methomyl and profenofos were given by gavages to male albino rats. These insecticides were administered daily for 28 days with doses equaled 1/20 LD 50 either singly or in a mixture of all the insecticides together. The study revealed significant decreases in body and kidneys weights, while increases in liver weights in all the treatments. Most of the treatments induced significant elevations in serum alanine aminotransferase [ALT] and aspartate aminotransferase [AST], while caused decreases in acetylcholinesterase [AChE] activities. Fenpropathrin and the mixture induced significant increase in total protein content of the serum, while the other treatments induced significant decreases. Creatinine concentrations recorded significant elevations in fenpropathrin and methomyl treatments, while significant decrease in case of Profenofos. Degenerative changes and granularity of hepatocytes with Kupffer cells activation were observed in the treatments with the mixture or and methomyl. Shrinking in Bowman's capsule and degenerative changes of epithelium lining renal tubules were observed in rats treated with the mixture. Moreover, necrotic changes associated with desquamation of epithelium lining tubules were shown in rats treated with the mixture, fenpropathrin and methomyl. From the biochemical data, the joint action was estimated for the mixture composed of the five insecticides. The mixture interacts antagonistically with most of the measured biochemical parameters

Alpha lipoic acid ameliorate changes occur in neurotransmitters and antioxidant enzymes that influenced by profenofos insecticide

This study was designed to determine whether alpha lipoic acid [ALA] which has been shown to have substantial antioxidant properties would ameliorate some of profenofos insecticide toxic effects. ALA administered [60mg/kg b.w.] to adult female rats for 14 days 1 hour after administration of 1/10 LD50 [45 mg/kg b.w.] and 1/20 LD50 [22.5 mg/kg b.w.] for profenofos insecticide which act as free radical inducer. Neurotransmitters [Dopamine [DA], Norepinephrin [NE], Serotonine [5-HT] and 5-Hydroxy indol acetic acid [5-HIAA]] were estimated in plasma. While malondialdehyde [MDA], reduced glutathione [GSH] level, glutathione-S-transferase [GST] and superoxide dismutase [SOD] activities were determined in liver, kidney and brain. The results revealed an increase in plasma serotonine [5-HT] levels in group of rats intoxicated with low dose of profenofos. A significant increase in MDA level [an indicator for lipid peroxidation] in liver of rats intoxicated with both doses of profenofos was recorded, concurrent with a significant reduction in GSH level and GST and SOD activities in most tested tissues of rats intoxicated with both doses of profenofos. Supplementation with alpha lipoic acid [60 mg/kg b.wt] 1 h after profenofos administration induced some but not complete improvement in all parameters whereas, it induced significant increase in plasma DA and 5-HT while it reduced lipid peroxidation in each of the examined tissues. These results accompanied with improvement in GSH level especially in liver, in addition to GST and SOD activities in some organs. Its effect differ from tissue to another. In conclusion ALA supplementation to profenofos intoxicated rats induced improvement in lipid peroxidation, total glutathione level and glutathione-S- transferase activity

Comparative haematological and hepatorenal toxicity of IGR, lufenuron and profenofos insecticide on albino rats

The present investigation was conducted to compare the toxicity of the IGR, lufenuron and the organophosphorus insecticide, profenofos on blood content, liver and kidney functions of male albino rats. The tested compounds were orally administered to rats at 1/20 and 1/10 of their median lethal doses [LD50s] for two months [day after another], then toxicants were withdrawn for 30 days to allow recovery of toxic effects. Data indicated that 1/10 LD50 of both compounds caused significant changes on blood contents and biochemical parameters of treated rats without return to normal levels at the end of recovery period, while, the smallest dose revealed negligible changes on some tested parameters with resumed normal values. The adverse effects reached its peak at 45 and 60 days of treatment [high dose treated rats] followed by decrease during recovery intervals without returned to normal, but at 1/10 LD50, lufenuron caused sever damage on kidney; urea and creatinine showed high levels at the end of recovery periods [92.0 and 220.0% above normal level, respectively]. Data indicated that, 1/10 LD50 of lufenuron treated rats exhibited changes in leucocytes, platelets counts, transaminases activities, creatinine and urea concentrations more than the organophosphorus insecticide. On the contrary, the same dose of profenofos mostly affected on erythrocytes counts, haemoglobin levels and alkaline phosphatase [ALP] activity. The obtained data would suggest that the two tested compounds at high dose have an inhibitory action on haemopiesis. In addition, both compounds proved to have comparable toxicity towards animals