ABSTRACT
CONTEXT: Nanoparticles may cause adverse environmental effects but there is limited information on their interactions with marine organisms. OBJECTIVE: Our aim was to examine the effects of triangular gold nanoparticles (Tr-Au NPs) on the clam, Ruditapes decussatus. MATERIALS AND METHODS: Clams were exposed to Tr-Au1 = 5 µg/L and Tr-Au2 = 10 µg/L for 2 and 7 days. Effects on shell structure were investigated. Superoxide dismutase (SOD), catalase (CAT), glutathione transferase (GST) activities, protein carbonyl levels and malondialdehyde content were used to assess biochemical status. RESULTS: Transmission electron microscopy (TEM) and electron dispersive X-ray microanalysis (EDX) showed that Tr-Au NPs modified shell structure and morphology. Tr-Au NPs size increased forming aggregate particles. Tr-Au NPs increased SOD, CAT and GST activities in gill and digestive gland in a concentration- and time-dependent manner indicating defence against oxidative stress. Enhanced lipid peroxidation and protein carbonyl levels confirmed oxidative stress. CONCLUSION: Tr-Au NPs cause oxidative stress and affect shell structure of clams. These findings may have relevance to other marine species.
Subject(s)
Animal Shells/metabolism , Bivalvia/anatomy & histology , Enzymes/metabolism , Gold/chemistry , Metal Nanoparticles/chemistry , Animal Shells/drug effects , Animal Shells/ultrastructure , Animals , Antioxidants/metabolism , Biomarkers/metabolism , Bivalvia/drug effects , Bivalvia/metabolism , Catalase/metabolism , Electron Probe Microanalysis , Gills/drug effects , Gills/metabolism , Glutathione Peroxidase/metabolism , Glutathione Transferase/metabolism , Gold/administration & dosage , Malondialdehyde/metabolism , Metal Nanoparticles/administration & dosage , Metal Nanoparticles/ultrastructure , Microscopy, Electron, Transmission , Superoxide Dismutase/metabolismABSTRACT
1. Laboratory experiments were carried out to assess uptake and metabolism of the epilepsy drug, carbamazepine and its consequent biological responses in marine clam (Ruditapes decussatus) a model non-target organism in ecotoxicology. 2. Clams were exposed to two nominal concentrations (C1 = 30 µg/L and C2 = 50 µg/L) of CBZ for a maximum period of 14 days. Analysis of CBZ and their metabolites in clam and water after exposure to two nominal concentrations of the pharmaceutical drug were performed using UPLC-HRMS analysis. CBZ accumulation reached an average tissue concentration of 1241.59 ng/g dw and 1664.33 ng/g dw at low and high nominal concentration, respectively. 3. Furthermore, a metabolite (3-hydroxy-CBZ) was detected in tissues indicating carbamazepine translocation and metabolism inside clam, suspect screening of CBZ glucuronides was also performed by accurate mass extraction but it could not be detected. 4. Activities of antioxidant enzymes superoxide dismutase, catalase and gluthatione-S-transferase generally increased. Change in the contents of glutathione, malondialdehyde and protein carbonyl were also studied. 5. Results indicated that the bioaccumulation of CBZ resulted in the changes of the antioxidant defense system and the production of ROS with the oxidative stress, ultimately induced alteration in lipid peroxidation and protein carbonyl.
Subject(s)
Bivalvia/metabolism , Carbamazepine/metabolism , Animals , Bivalvia/drug effects , Bivalvia/enzymology , Carbamazepine/toxicity , Catalase/metabolism , Gills/drug effects , Gills/metabolism , Glutathione/metabolism , Glutathione Transferase/metabolism , Malondialdehyde/metabolism , Metabolome/drug effects , Reference Standards , Superoxide Dismutase/metabolismABSTRACT
CONTEXT: Cypermethrin (CYP) is a synthetic pyrethroid insecticide used worldwide in agriculture, home pest control. The toxicity of CYP is well studied in many organisms. OBJECTIVE: The aim of present study was to investigate the protective effect of Zizyphus lotus (Zizyp) fruit against neurotoxicity and oxidative stress induced by CYP in mice. MATERIALS AND METHODS: Mice were divided into four groups of six each: groups I and II were used as control and CYP control (20 mg/kg body weight). While, groups III was orally treated with Zizyphus lotus fruit (5 g/kg body weight) plus CYP (20 mg/kg body weight) for 18 days. Furthermore, HPLC-ESI-MS-MS (Q-Tof) and GC-MS were used to identify the compounds fraction. RESULTS: Antioxidant enzyme catalase (CAT), neurotoxicity enzyme acetylcholinesterase (AChE) activities and hydrogen peroxide (H2O2), malondialdehyde (MDA) levels were determined in the liver, kidney and heart. CYP caused decreased CAT activity, inhibition of AChE activity and increased the levels of H2O2 and MDA in heart, liver and kidney. CONCLUSION: Our results indicate that Zizyp fruit is markedly effective in protecting mice against CYP-induced biochemical changes. This protection may be due to its antioxidant property and scavenging ability against active free radicals.
