TY - JOUR
T1 - Cadmium bound to metal rich granules and exoskeleton from Gammarus pulex causes increased gut lipid peroxidation in zebrafish following single dietary exposure
AU - Khan, F. R.
AU - Bury, N. R.
AU - Hogstrand, C.
PY - 2010/1/31
Y1 - 2010/1/31
N2 - There has been a growing interest in establishing how the sub-cellular distribution of metals in macro-invertebrate prey affects metal trophic bioavailability and toxicity. In this study, the crustacean Gammarus pulex was exposed to 300 mu g Cd l(-1) spiked with Cd-109 for 13 days, from which the two principal metal containing sub-cellular fractions, the metallothionein-like protein (MTLP) and the metal rich granule and exoskeleton (MRG + exo) were isolated. These fractions were produced at equal metal content, incorporated into gelatin and fed to zebrafish as a single meal; assimilation efficiency (AE), carcass and gut tissue metal concentrations and gut lipid peroxidative damage measured as malondialdehyde (MIDA) were assessed. The AE of cadmium bound to the MTLP fraction was 32.1 +/- 5.6% which was significantly greater than the AE of MRG + exo bound Cd, 13.0 +/- 2.1% (p <0.05). Of the metal retained by the fish at 72 h post-feeding, 94% of MTLP-Cd had been incorporated into the carcass, whereas a significant proportion (46%) of MRG + exo-Cd, although assimilated, appeared to remain associated with intestinal tissue. However, this did not translate into a gut tissue concentration difference with 6.8 +/- 1.2 ng Cd g(-1) in fish fed MTLP-Cd compared to 9.5 +/- 1.4 ng C dg(-1) in fish fed MRG + exo fraction. Both feeds led to significantly increased MDA levels compared to the control group (gelatin only feed), but MRG + exo feed caused significantly more oxidative damage than the MTLP feed (p <0.01). Thus, MTLP-Cd is more bioavailable than the cadmium bound to granules and exoskeleton, but it was the latter fraction, largely considered as having limited bioavailability, that appeared to exert a greater localised oxidative injury to the digestive tract of zebrafish. (C) 2009 Elsevier B.V. All rights reserved.
AB - There has been a growing interest in establishing how the sub-cellular distribution of metals in macro-invertebrate prey affects metal trophic bioavailability and toxicity. In this study, the crustacean Gammarus pulex was exposed to 300 mu g Cd l(-1) spiked with Cd-109 for 13 days, from which the two principal metal containing sub-cellular fractions, the metallothionein-like protein (MTLP) and the metal rich granule and exoskeleton (MRG + exo) were isolated. These fractions were produced at equal metal content, incorporated into gelatin and fed to zebrafish as a single meal; assimilation efficiency (AE), carcass and gut tissue metal concentrations and gut lipid peroxidative damage measured as malondialdehyde (MIDA) were assessed. The AE of cadmium bound to the MTLP fraction was 32.1 +/- 5.6% which was significantly greater than the AE of MRG + exo bound Cd, 13.0 +/- 2.1% (p <0.05). Of the metal retained by the fish at 72 h post-feeding, 94% of MTLP-Cd had been incorporated into the carcass, whereas a significant proportion (46%) of MRG + exo-Cd, although assimilated, appeared to remain associated with intestinal tissue. However, this did not translate into a gut tissue concentration difference with 6.8 +/- 1.2 ng Cd g(-1) in fish fed MTLP-Cd compared to 9.5 +/- 1.4 ng C dg(-1) in fish fed MRG + exo fraction. Both feeds led to significantly increased MDA levels compared to the control group (gelatin only feed), but MRG + exo feed caused significantly more oxidative damage than the MTLP feed (p <0.01). Thus, MTLP-Cd is more bioavailable than the cadmium bound to granules and exoskeleton, but it was the latter fraction, largely considered as having limited bioavailability, that appeared to exert a greater localised oxidative injury to the digestive tract of zebrafish. (C) 2009 Elsevier B.V. All rights reserved.
U2 - 10.1016/j.aquatox.2009.10.010
DO - 10.1016/j.aquatox.2009.10.010
M3 - Article
VL - 96
SP - 124
EP - 129
JO - AQUATIC TOXICOLOGY
JF - AQUATIC TOXICOLOGY
IS - 2
ER -