2022
DOI: 10.1016/j.etap.2022.103888
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Comparison of cellular mechanisms induced by pharmaceutical exposure to caffeine and its combination with salicylic acid in mussel Mytilus galloprovincialis

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Cited by 13 publications
(3 citation statements)
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“…Being stained by Masson trichrome with aniline blue, the chitinous rod is made up of connective tissue, and its break could be related to mechanical damage of MPs since it has been demonstrated that they can reach this anatomical district (Von Moos et al, 2012). The hemocyte infiltration could be caused not only by the break of the chitinous rod but also as a response of defense from pollutants, indeed it is caused also by caffeine as demonstrated by our results and other experimentation (De Marco, Afsa, Galati, Billè, & Parrino, 2022; De Marco, Afsa, Galati, Guerriero, et al, 2022) and it is also provoked by other pollutants (De Marco et al, 2023; Speciale et al, 2018). Another defense mechanism could be the hemocytic aggregation in the gill filament after caffeine exposure which impairs hemolymph flow inside the filament.…”
Section: Discussionsupporting
confidence: 80%
“…Being stained by Masson trichrome with aniline blue, the chitinous rod is made up of connective tissue, and its break could be related to mechanical damage of MPs since it has been demonstrated that they can reach this anatomical district (Von Moos et al, 2012). The hemocyte infiltration could be caused not only by the break of the chitinous rod but also as a response of defense from pollutants, indeed it is caused also by caffeine as demonstrated by our results and other experimentation (De Marco, Afsa, Galati, Billè, & Parrino, 2022; De Marco, Afsa, Galati, Guerriero, et al, 2022) and it is also provoked by other pollutants (De Marco et al, 2023; Speciale et al, 2018). Another defense mechanism could be the hemocytic aggregation in the gill filament after caffeine exposure which impairs hemolymph flow inside the filament.…”
Section: Discussionsupporting
confidence: 80%
“…The supernatants were collected and kept at −20 °C until the analysis of oxidative stress biomarkers [ 52 ] including lipid peroxidation (LPO) [ 56 ], glutathione (GSH) [ 57 ], and catalase (CAT) [ 58 ] by applying their respective protocols. Specifically, to estimate LPO, a measurement of malondialdehyde (MDA; nmol/mg protein) was performed by applying the thiobarbituric acid reactive (TBARS) method as described in detail elsewhere [ 59 , 60 ]. The reduced GSH was estimated using the colorimetric Ellman’s method [ 61 ], treating the tissue homogenate with trichloroacetic acid (TCA) 10%, and then adding 0.2 M Tris EDTA buffer in order to prevent GSH oxidation.…”
Section: Methodsmentioning
confidence: 99%
“…The reduced GSH was estimated using the colorimetric Ellman’s method [ 61 ], treating the tissue homogenate with trichloroacetic acid (TCA) 10%, and then adding 0.2 M Tris EDTA buffer in order to prevent GSH oxidation. In addition, the enzymatic activity of CAT (μmol/min/mg protein) was evaluated following the dismutation of H 2 O 2 at 240 nm for 90 s using a colorimetric technique [ 59 , 60 ].…”
Section: Methodsmentioning
confidence: 99%