Pesticides can enter aquatic environments potentially affecting non-target organisms. Unfortunately, the effects of such substances are still poorly understood. This study investigated the effects of the active neonicotinoid substance thiacloprid (TH) and the commercial product Calypso 480 SC (CA) (active compound 40.4% TH) on Mytilus galloprovincialis after short-term exposure to sublethal concentrations. Mussels were tested for seven days to 0, 1, 5 and 10 mg L-1 TH and 0, 10, 50 and 100 mg L-1 CA. For this purpose, several parameters, such as cell viability of haemocytes and digestive cells, biochemical haemolymph features, superoxide dismutase (SOD) and catalase (CAT) enzymatic activity of gills and digestive gland, as well as histology of such tissues were analysed. The sublethal concentrations of both substances lead to abatement or completely stopping the byssal fibres creation. Biochemical analysis of haemolymph showed significant changes (P < 0.01) in electrolytes ions (Cl-, K+, Na+, Ca2+, S-phosphor), lactate dehydrogenase (LDH) enzyme activity and glucose concentration following exposure to both substances. The TH-exposed mussels showed significant imbalance (P < 0.05) in CAT activity in digestive gland and gills. CA caused significant decrease (P < 0.05) in SOD activity in gills and in CAT activity in both tissues. Results of histological analyses showed severe damage in both digestive gland and gills in a time- and concentration-dependent manner. This study provides useful information about the acute toxicity of a neonicotinoid compound and a commercial insecticide on mussels. Nevertheless, considering that neonicotinoids are still widely used and that mussels are very important species for marine environment and human consumption, further researches are needed to better comprehend the potential risk posed by such compounds to aquatic non-target species.
- MeSH
- Water Pollutants, Chemical toxicity MeSH
- Hemocytes drug effects MeSH
- Hemolymph drug effects MeSH
- Insecticides toxicity MeSH
- Catalase metabolism MeSH
- Mytilus drug effects MeSH
- Neonicotinoids toxicity MeSH
- Superoxide Dismutase metabolism MeSH
- Toxicity Tests, Acute MeSH
- Thiazines toxicity MeSH
- Cell Survival MeSH
- Dose-Response Relationship, Drug MeSH
- Gills drug effects enzymology MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
The Gulf of Follonica (Italy) is impacted by the chemical pollution from ancient mining activity and present industrial processes. This study was aimed to determine the bioavailability of dioxin-like compounds (DLCs) in coastal marine environment and to assess the genotoxic potential of waste waters entering the sea from an industrial canal. Moderately high levels of DCLs compounds (∑ PCDDs + PCDFs 2.18–29.00 pg/g dry wt) were detected in Mytilus galloprovincialis transplanted near the waste waters canal and their corresponding Toxic Equivalents (TEQs) calculated. In situ exposed mussels did not show any genotoxic effect (by Comet and Micronucleus assay). Otherwise, laboratory exposure to canal waters exhibited a reduced genomic template stability (by RAPD-PCR assay) but not DNA or chromosomal damage. Our data reveal the need to focus on the levels and distribution of DLCs in edible species from the study area considering their potential transfer to humans through the consumption of sea food.
- MeSH
- Biological Availability MeSH
- Water Pollutants, Chemical analysis toxicity MeSH
- Dioxins analysis toxicity MeSH
- Humans MeSH
- Environmental Monitoring methods MeSH
- Mutagens analysis chemistry toxicity MeSH
- Mytilus drug effects genetics MeSH
- Random Amplified Polymorphic DNA Technique MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Italy MeSH
- MeSH
- Antioxidants therapeutic use MeSH
- Chondroitin administration & dosage adverse effects therapeutic use MeSH
- Diet Therapy * classification methods utilization MeSH
- Glucosamine administration & dosage adverse effects therapeutic use MeSH
- Collagen administration & dosage adverse effects therapeutic use MeSH
- Hyaluronic Acid administration & dosage adverse effects therapeutic use MeSH
- Plants, Medicinal MeSH
- Mytilus edulis MeSH
- Joint Diseases * drug therapy MeSH
- Cat Diseases MeSH
- Dog Diseases MeSH
- Plant Oils therapeutic use MeSH
- Fatty Acids, Omega-3 administration & dosage adverse effects therapeutic use MeSH
- Persea MeSH
- Dietary Supplements * classification utilization MeSH
- Statistics as Topic MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
Despite the growing concern over the potential biological impact of nanoparticles (NPs) in the aquatic environment, little is known about their interactions with other pollutants. The bivalve Mytilus sp, largely utilized as a sentinel for marine contamination, has been shown to represent a significant target for different types of NP, including n-TiO2, one of the most widespread in use. In this work, the possible interactive effects of n-TiO2 and 2,3,7,8-TCDD, chosen as models of NP and organic contaminant, respectively, were investigated in Mytilus galloprovincialis. In vitro experiments with n-TiO2 and TCDD, alone and in combination, were carried out in different conditions (concentrations and times of exposure), depending on the target (hemocytes, gill cells and biopsies) and the endpoint measured. Mussels were also exposed in vivo to n-TiO2 (100 μg L(-1)) or to TCDD (0.25 μg L(-1)), alone and in combination, for 96 h. A wide range of biomarkers, from molecular to tissue level, were measured: lysosomal membrane stability and phagocytosis in hemocytes, ATP-binding cassette efflux transporters in gills (gene transcription and efflux activity), several biomarkers of genotoxicity in gill and digestive cells (DNA damage, random amplified polymorphic DNA-RAPD changes), lysosomal biomarkers and transcription of selected genes in the digestive gland. The results demonstrate that n-TiO2 and TCDD can exert synergistic or antagonistic effects, depending on experimental condition, cell/tissue and type of measured response. Some of these interactions may result from a significant increase in TCDD accumulation in whole mussel organisms in the presence of n-TiO2, indicating a Trojan horse effect. The results represent the most extensive data obtained so far on the sub-lethal effects of NPs and organic contaminants in aquatic organisms. Moreover, these data extend the knowledge on the molecular and cellular targets of NPs in bivalves.
- MeSH
- Biomarkers analysis MeSH
- Water Pollutants, Chemical metabolism toxicity MeSH
- Phagocytosis drug effects MeSH
- Hemocytes drug effects MeSH
- Drug Interactions MeSH
- Lysosomes drug effects MeSH
- Mytilus drug effects genetics metabolism MeSH
- Nanoparticles toxicity MeSH
- Polychlorinated Dibenzodioxins metabolism toxicity MeSH
- DNA Damage drug effects MeSH
- Random Amplified Polymorphic DNA Technique MeSH
- Titanium toxicity MeSH
- Gills drug effects MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
For over 30 years empirical studies have repeatedly demonstrated that the biosynthesis of morphine by diverse animal and human tissues occurs. Recently, the blue mussel's neural tissues and human white blood cells were used to demonstrate the de novo biosynthesis of morphine for small precursor molecules derived from the aromatic amino acid L-tyrosine. Because catecholamine precursors, i.e., L-3,4-dihydroxyphenylalanine (L-DOPA), were also found to be utilized as morphine precursors, a novel reciprocally interactive mechanism is apparent that links catecholamine and opioid pathways in the activation and inhibition of diverse tissue responses. Additionally, these observations provide new insights into morphinergic signalling that transcend analgesia and addiction. We have also linked the biological effects of nitric oxide into a common effect in endogenous morphine signalling. Given the singular importance of dopamine and morphine's interaction in the CNS, the presence and association of this signalling with nitric oxide all promises to provide novel answers for mental health phenomena, which have been lacking because of the inability in accepting the empirical endogenous morphine studies.
- MeSH
- Dopamine pharmacology MeSH
- Catecholamines metabolism MeSH
- Leukocytes metabolism MeSH
- Levodopa metabolism MeSH
- Humans MeSH
- Morphine biosynthesis pharmacology MeSH
- Mytilus edulis metabolism MeSH
- Opioid Peptides metabolism MeSH
- Nitric Oxide pharmacology MeSH
- Signal Transduction MeSH
- Tyrosine metabolism MeSH
- Morphine Dependence psychology MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Review MeSH