Article detail · 2014 · article
In vivo changes in carbonic anhydrase activity and histopathology of gill and liver tissues after acute exposure to chlorpyrifos in rainbow trout
Data source split
- YÖKSİSYÖKSİS article record
- YÖKSİS venueArchives of Industrial Hygiene and Toxicology
- Catalog match (ISSN)Arhiv za Higijenu Rada i Toksikologiju
- OpenAlexOpenAlex enrichment (abstract, citations, topics)
- Semantic Scholarcitation count (not merged with OpenAlex)
Abstract
Chlorpyrifos is an organophosphate pesticide widely used in agriculture and aquaculture. This study investigated its effects on carbonic anhydrase (CA) enzyme activity and histopathology of rainbow trout gill and liver. The fish were exposed to 2.25 (25% of 96 h LC50), 4.5 (50% of 96 h LC50), and 6.75 μg L⁻¹ (75% of 96 h LC50) of chlorpyrifos for 24, 48, 72, and 96 h. CA activity was measured in liver and gills and histopathological changes were examined by light microscopy. The most common liver changes at most of the chlorpyrifos concentrations were hyperaemia and degenerative changes. Gill tissues were characterised by lamellar hyperaemia, lamellar oedemas, clumping, cellular degeneration, hyperplasia, and lamellar atrophy. CA enzyme activity in the gills decreased at all concentrations at 48, 72, and 96 h after exposure to chlorpyrifos (p<0.05). Similarly, there was a time-dependent decrease in CA activity at all of the concentrations in liver tissues (p<0.05). The present study indicated that chlorpyrifos inhibits CA enzyme activity and causes histopathological damage in gill and liver tissues.
Topics
Citations
OpenAlex cited_by_count. Not a WoS or Scopus citation count; those sources have no separate column here.
61citationsOpenAlex · cited_by_count (cache / database)
89 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).
- 2019 Synthesis, biological evaluation and in silico studies of novel N-substituted phthalazine sulfonamide compounds as potent carbonic anhydrase and acetylcholinesterase inhibitorsCitations 136 · OpenAlex
- 2019 Synthesis, biological evaluation and in silico studies of novel N-substituted phthalazine sulfonamide compounds as potent carbonic anhydrase and acetylcholinesterase inhibitorsCitations 135 · OpenAlex
- 2019 Synthesis, biological evaluation and in silico studies of novel N-substituted phthalazine sulfonamide compounds as potent carbonic anhydrase and acetylcholinesterase inhibitorsCitations 135 · OpenAlex
- 2019 Synthesis, biological evaluation and in silico studies of novel N-substituted phthalazine sulfonamide compounds as potent carbonic anhydrase and acetylcholinesterase inhibitorsCitations 135 · OpenAlex
- 2021 Novel benzoic acid derivatives: Synthesis and biological evaluation as multitarget acetylcholinesterase and carbonic anhydrase inhibitorsCitations 93 · OpenAlex
- 2021 Novel benzoic acid derivatives: Synthesis and biological evaluation as multitarget acetylcholinesterase and carbonic anhydrase inhibitorsCitations 93 · OpenAlex
- 2020 Novel benzoic acid derivatives: Synthesis and biological evaluation as multitarget acetylcholinesterase and carbonic anhydrase inhibitorsCitations 93 · OpenAlex
- 2021 Calcium channel blockers: molecular docking and inhibition studies on carbonic anhydrase I and II isoenzymesCitations 86 · OpenAlex
- 2021 Calcium channel blockers: molecular docking and inhibition studies on carbonic anhydrase I and II isoenzymesCitations 86 · OpenAlex
- 2020 Calcium channel blockers: molecular docking and inhibition studies on carbonic anhydrase I and II isoenzymesCitations 86 · OpenAlex