Branchial versus intestinal silver toxicity and uptake in the marine teleost Parophrys vetulus

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Standard

Branchial versus intestinal silver toxicity and uptake in the marine teleost Parophrys vetulus. / Grosell, Martin Hautopp; Wood, C. M.

I: Journal of Comparative Physiology. B, Biochemical, Systemic, and Environmental Physiology, Bind 171, Nr. 7, 2001, s. 585-594.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Grosell, MH & Wood, CM 2001, 'Branchial versus intestinal silver toxicity and uptake in the marine teleost Parophrys vetulus', Journal of Comparative Physiology. B, Biochemical, Systemic, and Environmental Physiology, bind 171, nr. 7, s. 585-594. https://doi.org/10.1007/s003600100209

APA

Grosell, M. H., & Wood, C. M. (2001). Branchial versus intestinal silver toxicity and uptake in the marine teleost Parophrys vetulus. Journal of Comparative Physiology. B, Biochemical, Systemic, and Environmental Physiology, 171(7), 585-594. https://doi.org/10.1007/s003600100209

Vancouver

Grosell MH, Wood CM. Branchial versus intestinal silver toxicity and uptake in the marine teleost Parophrys vetulus. Journal of Comparative Physiology. B, Biochemical, Systemic, and Environmental Physiology. 2001;171(7):585-594. https://doi.org/10.1007/s003600100209

Author

Grosell, Martin Hautopp ; Wood, C. M. / Branchial versus intestinal silver toxicity and uptake in the marine teleost Parophrys vetulus. I: Journal of Comparative Physiology. B, Biochemical, Systemic, and Environmental Physiology. 2001 ; Bind 171, Nr. 7. s. 585-594.

Bibtex

@article{f940e28074c511dbbee902004c4f4f50,
title = "Branchial versus intestinal silver toxicity and uptake in the marine teleost Parophrys vetulus",
abstract = "Exposure to elevated waterborne silver as AgNO3 (4.07 µM=448 µg l-1) in seawater resulted in osmoregulatory disturbance in the lemon sole (Parophrys vetulus). The main effects were increased plasma Na+ and Cl- concentrations which translated into increased plasma osmolality. Plasma Mg2+ levels were also slightly increased after 96 h exposure. Using radio-isotopic flux measurements, a 50% reduction in branchial unidirectional Na+ extrusion was observed after 48 h silver exposure. By applying an intestinal perfusion approach, we were able to separate and thus quantify the intestinal contribution to the observed silver-induced physiological disturbance and internal silver accumulation. This analysis revealed that the intestinal contribution to silver-induced ionoregulatory toxicity was as high as 50-60%. In marked contrast, internal silver accumulation (in liver and kidney) was found to be derived exclusively from uptake across the gills. Drinking of silver-contaminated seawater resulted in substantial silver accumulation in the intestinal tissue (but apparently not silver uptake across the intestine), which probably explains the intestinal contribution to silver-induced physiological disturbance.",
author = "Grosell, {Martin Hautopp} and Wood, {C. M.}",
year = "2001",
doi = "10.1007/s003600100209",
language = "English",
volume = "171",
pages = "585--594",
journal = "Journal of Comparative Physiology B: Biochemical, Systemic, and Environmental Physiology",
issn = "0174-1578",
publisher = "Springer",
number = "7",

}

RIS

TY - JOUR

T1 - Branchial versus intestinal silver toxicity and uptake in the marine teleost Parophrys vetulus

AU - Grosell, Martin Hautopp

AU - Wood, C. M.

PY - 2001

Y1 - 2001

N2 - Exposure to elevated waterborne silver as AgNO3 (4.07 µM=448 µg l-1) in seawater resulted in osmoregulatory disturbance in the lemon sole (Parophrys vetulus). The main effects were increased plasma Na+ and Cl- concentrations which translated into increased plasma osmolality. Plasma Mg2+ levels were also slightly increased after 96 h exposure. Using radio-isotopic flux measurements, a 50% reduction in branchial unidirectional Na+ extrusion was observed after 48 h silver exposure. By applying an intestinal perfusion approach, we were able to separate and thus quantify the intestinal contribution to the observed silver-induced physiological disturbance and internal silver accumulation. This analysis revealed that the intestinal contribution to silver-induced ionoregulatory toxicity was as high as 50-60%. In marked contrast, internal silver accumulation (in liver and kidney) was found to be derived exclusively from uptake across the gills. Drinking of silver-contaminated seawater resulted in substantial silver accumulation in the intestinal tissue (but apparently not silver uptake across the intestine), which probably explains the intestinal contribution to silver-induced physiological disturbance.

AB - Exposure to elevated waterborne silver as AgNO3 (4.07 µM=448 µg l-1) in seawater resulted in osmoregulatory disturbance in the lemon sole (Parophrys vetulus). The main effects were increased plasma Na+ and Cl- concentrations which translated into increased plasma osmolality. Plasma Mg2+ levels were also slightly increased after 96 h exposure. Using radio-isotopic flux measurements, a 50% reduction in branchial unidirectional Na+ extrusion was observed after 48 h silver exposure. By applying an intestinal perfusion approach, we were able to separate and thus quantify the intestinal contribution to the observed silver-induced physiological disturbance and internal silver accumulation. This analysis revealed that the intestinal contribution to silver-induced ionoregulatory toxicity was as high as 50-60%. In marked contrast, internal silver accumulation (in liver and kidney) was found to be derived exclusively from uptake across the gills. Drinking of silver-contaminated seawater resulted in substantial silver accumulation in the intestinal tissue (but apparently not silver uptake across the intestine), which probably explains the intestinal contribution to silver-induced physiological disturbance.

U2 - 10.1007/s003600100209

DO - 10.1007/s003600100209

M3 - Journal article

VL - 171

SP - 585

EP - 594

JO - Journal of Comparative Physiology B: Biochemical, Systemic, and Environmental Physiology

JF - Journal of Comparative Physiology B: Biochemical, Systemic, and Environmental Physiology

SN - 0174-1578

IS - 7

ER -

ID: 142844