2022
DOI: 10.1016/j.bbrep.2022.101217
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Effects of chemical forms of gadolinium on the spleen in mice after single intravenous administration

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Cited by 7 publications
(7 citation statements)
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“…The level was highest for gadodiamide [ 62 ]. In mice, high doses were found in the kidneys after high-dose gadodiamide (7.49 nmol/g tissue) or gadobutrol (16.36 nmol/g tissue) administration, but no spleen enlargement was found after GBCA administration [ 63 ]. In subtotally nephrectomised rats, higher Gd levels 28 days after administration of gadobutrol or gadoterate versus gadoteridol were determined in the kidneys and liver.…”
Section: Introductionmentioning
confidence: 99%
“…The level was highest for gadodiamide [ 62 ]. In mice, high doses were found in the kidneys after high-dose gadodiamide (7.49 nmol/g tissue) or gadobutrol (16.36 nmol/g tissue) administration, but no spleen enlargement was found after GBCA administration [ 63 ]. In subtotally nephrectomised rats, higher Gd levels 28 days after administration of gadobutrol or gadoterate versus gadoteridol were determined in the kidneys and liver.…”
Section: Introductionmentioning
confidence: 99%
“…Nowadays, only small gadolinium-based organic molecules have been FDA-approved as positive contrast agents for nanomedicine . However, they suffer from several disadvantages, like potential biotoxicity, fast clearance from the body and thus short circulation times, as well as undesired accumulation of gadolinium ions in human tissues . To overcome these drawbacks, it is possible to incorporate paramagnetic ions inside size-tunable nanoparticles, exhibiting lower toxicity and increased retention within the body …”
Section: Resultsmentioning
confidence: 99%
“…Nakamura et al, 2022 [29] BALB/c male mice treated with a single administration of Omniscan™ (gadodiamide), Gadovist ® (gadobutrol), or Gd (III) in the form of Gd(NO 3 ) 3 or GdCl 3…”
Section: Reference Study Design Main Findingsmentioning
confidence: 99%
“…Other plausible mechanisms underlying Gd (III) toxicity include blockage of adenosine diphosphate and adenosine triphosphate (ATP) hydrolysis through stimulation of angiotensin II AT1 receptors [78]; inhibition of ATP-permeable channels [106]; interference with the epithelial Na + -channel's activity [63]; downregulation of RhoA, mTORC1, and mTORC2 proteins [31]; and inhibition on both inward and outward ionic current through Gd (III) accumulation at the binding site of the Na + -Ca 2+ exchanger protein that carries the current [104]. It may also interfere with the mobilization of iron [29,67], as it has been associated with total iron-binding capacity (TIBC) decrease [75], and to increases in serum iron, ferritin [41,75,80], and transferrin saturation [75]. It also has an effect on the differentiation of mononuclear cells into ferroportin-expressing fibrocytic cells [67] and the differentiation of mononuclear cells into collagen-secreting cells, with increased expression of iron metabolism proteins and of angiogenic and osteoblast-lineage markers [73].…”
Section: Reference Study Design Main Findingsmentioning
confidence: 99%