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1.
Mar Pollut Bull ; 172: 112853, 2021 Nov.
Article in English | MEDLINE | ID: mdl-34425367

ABSTRACT

We provided the first multi-species study investigating the presence and organotropism of trace elements in three tissues of 12 elasmobranch species. Shark species showed comparable TE loads, although milk sharks and juvenile scalloped hammerhead sharks exhibited the highest Cd and Hg levels, respectively. Fins accumulated higher levels of Pb, Co, and Cr; muscles higher V, As, and Hg; livers higher Se and Cd levels. The organotropism of TEs calls for cautious when choosing a tissue to be sampled since certain tissues, like fin clips, do not provide reliable surrogate for the internal loads of some TEs. Strong correlations between essential and toxic TEs indicated detoxification mechanisms, while the TMF provided evidence for Hg, As and Se biomagnification along the food-web. Considering the difficulties in assessing elasmobranchs contamination from different areas, the proposed multi-species approach represents a valuable way to estimate the species-specific accumulation and transfer of pollutants in sharks.


Subject(s)
Sharks , Trace Elements , Water Pollutants, Chemical , Animals , Bioaccumulation , Environmental Monitoring , Food Chain , Indian Ocean , Trace Elements/analysis , Water Pollutants, Chemical/analysis
2.
J Chemother ; 23(5): 273-6, 2011 Oct.
Article in English | MEDLINE | ID: mdl-22005058

ABSTRACT

Human immunodeficiency virus 1 (HIV-1) and Hepatitis C virus (HCV) affect 60 and 170 million infected individuals worldwide, respectively, and co-infection by both pathogens is often observed. This represents a serious public health problem that requires the identification of new drugs targeting essential phases of the life cycle of these two viruses. In this report, the synthesis and inhibitory activity of quinizarin derivatives towards both HCV NS5B polymerase and HIV-1 reverse transcriptase associated functions are reported. Our results demonstrate that anthraquinone derivatives are promising anti-polymerase viral inhibitors.


Subject(s)
Anthraquinones/pharmacology , Drug Design , HIV Reverse Transcriptase/antagonists & inhibitors , HIV-1/drug effects , Hepacivirus/drug effects , Reverse Transcriptase Inhibitors/pharmacology , Ribonuclease H, Human Immunodeficiency Virus/antagonists & inhibitors , Viral Nonstructural Proteins/antagonists & inhibitors , Anthraquinones/adverse effects , Anthraquinones/chemistry , Anti-HIV Agents/adverse effects , Anti-HIV Agents/chemistry , Anti-HIV Agents/pharmacology , Cell Line , Cell Survival/drug effects , DNA-Directed RNA Polymerases/antagonists & inhibitors , DNA-Directed RNA Polymerases/genetics , HIV Infections/complications , HIV Infections/drug therapy , HIV Reverse Transcriptase/genetics , HIV-1/enzymology , Hepacivirus/enzymology , Hepatitis C/complications , Hepatitis C/drug therapy , Humans , Inhibitory Concentration 50 , Intercalating Agents/adverse effects , Intercalating Agents/chemistry , Intercalating Agents/pharmacology , RNA-Dependent RNA Polymerase/antagonists & inhibitors , RNA-Dependent RNA Polymerase/genetics , Recombinant Proteins/antagonists & inhibitors , Replicon/drug effects , Reverse Transcriptase Inhibitors/adverse effects , Reverse Transcriptase Inhibitors/chemistry , Ribonuclease H, Human Immunodeficiency Virus/genetics , Structure-Activity Relationship , Viral Nonstructural Proteins/genetics , Virus Replication/drug effects
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