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Rui Rosa,Catarina Santos,Ana Lopes,Miguel Baptista,Eduardo Sampaio,Inês C. Rosa,Tiago Repolho 한국해양과학기술원 2019 Ocean science journal Vol.54 No.2
Tetracosapolyenoic fatty acids (TPA), namely tetracosapentaenoic (24:5n-6) and tetracosahexaenoic (24:6n-3) acids, are chemotaxonomic biomarkers of octocorals (Cnidaria, Octocorallia) in the marine environment. The present study confirms the occurrence of TPA on a marine non-cnidarian taxon, the nudibranch mollusc Armina maculata. This discovery is explained by the specialized feeding regime (stenophagy) of this sea slug that preys upon the octocoral Veretillum cynomorium. The prevalence of 24:5n-6 and 24:6n-3 in the body of A. maculata was demonstrated through the analysis of specimens starved for 30 days in captivity. Since the time frame is superior to the residence time of ingested octocorals, the present findings provide empirical evidence that the reported TPA are allocated from nudibranch tissues. Here we found support for previous claims that the presence of TPA in the marine tree of life is not restricted to its lower branches, as stenophagous trophic interactions may allow its transfer to or posterior biosynthesis in more evolved taxa.
Silva-Carvalho, Ricardo,Silva, Joao P.,Ferreirinha, Pedro,Leitao, Alexandre F.,Andrade, Fabia K.,da Costa, Rui M. Gil,Cristelo, Cecilia,Rosa, Morsyleide F.,Vilanova, Manuel,Gama, F. Miguel Korean Society of ToxicologyKorea Environmental Mu 2019 Toxicological Research Vol.35 No.1
In view of the growing industrial use of Bacterial cellulose (BC), and taking into account that it might become airborne and be inhaled after industrial processing, assessing its potential pulmonary toxic effects assumes high relevance. In this work, the murine model was used to assess the effects of exposure to respirable BC nanofibrils (nBC), obtained by disintegration of BC produced by Komagataeibacter hansenii. Murine bone marrow-derived macrophages ($BMM{\Phi}$) were treated with different doses of nBC (0.02 and 0.2 mg/mL, respectively 1 and $10{\mu}g$ of fibrils) in absence or presence of 0.2% Carboxymethyl Cellulose (nBCMC). Furthermore, mice were instilled intratracheally with nBC or nBCMC at different concentrations and at different time-points and analyzed up to 6 months after treatments. Microcrystaline $Avicel-plus^{(R)}$ CM 2159, a plant-derived cellulose, was used for comparison. Markers of cellular damage (lactate dehydrogenase release and total protein) and oxidative stress (hydrogen peroxidase, reduced glutathione, lipid peroxidation and glutathione peroxidase activity) as well presence of inflammatory cells were evaluated in brochoalveolar lavage (BAL) fluids. Histological analysis of lungs, heart and liver tissues was also performed. BAL analysis showed that exposure to nBCMC or CMC did not induce major alterations in the assessed markers of cell damage, oxidative stress or inflammatory cell numbers in BAL fluid over time, even following cumulative treatments. $Avicel-plus^{(R)}$ CM 2159 significantly increased LDH release, detected 3 months after 4 weekly administrations. However, histological results revealed a chronic inflammatory response and tissue alterations, being hypertrophy of pulmonary arteries (observed 3 months after nBCMC treatment) of particular concern. These histological alterations remained after 6 months in animals treated with nBC, possibly due to foreign body reaction and the organism's inability to remove the fibers. Overall, despite being a safe and biocompatible biomaterial, BC-derived nanofibrils inhalation may lead to lung pathology and pose significant health risks.
Ricardo Silva-Carvalho,Joao P. Silva,Pedro Ferreirinha,Alexandre F. Leitao,Fabia K. Andrade,Rui M. Gil da Costa,Cecilia Cristelo,Morsyleide F. Rosa,Manuel Vilanova,F. Miguel Gama 한국독성학회 2019 Toxicological Research Vol.35 No.1
In view of the growing industrial use of Bacterial cellulose (BC), and taking into account that it might become airborne and be inhaled after industrial processing, assessing its potential pulmonary toxic effects assumes high relevance. In this work, the murine model was used to assess the effects of exposure to respirable BC nanofibrils (nBC), obtained by disintegration of BC produced by Komagataeibacter hansenii. Murine bone marrow-derived macrophages (BMMΦ) were treated with different doses of nBC (0.02 and 0.2 mg/mL, respectively 1 and 10 μg of fibrils) in absence or presence of 0.2% Carboxymethyl Cellulose (nBCMC). Furthermore, mice were instilled intratracheally with nBC or nBCMC at different concentrations and at different time-points and analyzed up to 6 months after treatments. Microcrystaline Avicel-plus® CM 2159, a plant-derived cellulose, was used for comparison. Markers of cellular damage (lactate dehydrogenase release and total protein) and oxidative stress (hydrogen peroxidase, reduced glutathione, lipid peroxidation and glutathione peroxidase activity) as well presence of inflammatory cells were evaluated in brochoalveolar lavage (BAL) fluids. Histological analysis of lungs, heart and liver tissues was also performed. BAL analysis showed that exposure to nBCMC or CMC did not induce major alterations in the assessed markers of cell damage, oxidative stress or inflammatory cell numbers in BAL fluid over time, even following cumulative treatments. Avicel-plus® CM 2159 significantly increased LDH release, detected 3 months after 4 weekly administrations. However, histological results revealed a chronic inflammatory response and tissue alterations, being hypertrophy of pulmonary arteries (observed 3 months after nBCMC treatment) of particular concern. These histological alterations remained after 6 months in animals treated with nBC, possibly due to foreign body reaction and the organism’s inability to remove the fibers. Overall, despite being a safe and biocompatible biomaterial, BC-derived nanofibrils inhalation may lead to lung pathology and pose significant health risks.