1942
DOI: 10.1172/jci101321
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The Anticoagulant Effects in Rabbits and Man of the Intravenous Injection of Salts of the Rare Earths

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Cited by 33 publications
(7 citation statements)
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“…Lu was reported to be accumulated in the bones (much), liver, and kidneys, although there was no information for the biological effects. Holmium (Ho) and thulium (Tm) compounds are known to stimulate the metabolism of the human body, but their biological effects are still controversial [12], [29], [43]. Dermal fibrosis (nephrogenic systemic fibrosis) was reported by gadolinium (Gd) used as contrast agents for magnetic resonance images [44].…”
Section: Resultsmentioning
confidence: 99%
“…Lu was reported to be accumulated in the bones (much), liver, and kidneys, although there was no information for the biological effects. Holmium (Ho) and thulium (Tm) compounds are known to stimulate the metabolism of the human body, but their biological effects are still controversial [12], [29], [43]. Dermal fibrosis (nephrogenic systemic fibrosis) was reported by gadolinium (Gd) used as contrast agents for magnetic resonance images [44].…”
Section: Resultsmentioning
confidence: 99%
“…The rare earth metals have a retarding effect on blood coagulation (Steidle 1935, Vincke & Oelkers 1937, Beaser et al 1942, Hara & Sat0 1955. This property of the lanthanons led to exploration for a non-toxic lanthanon compound which could be utilized as an anti-thrombotic agent (Vincke 1955).…”
Section: A ) Il'ithin Industrymentioning
confidence: 99%
“…First described in the early 1930s [12], in 1937 Vincke and Oelkers reported another until then rather unknown property of rare earth metals, the anticoagulant potential, without being able to further clarify their mode of action [33]. At that time different rare earths were even proposed for use as therapeutic anticoagulation agents [7,33], which was later revised as inexpedient because of unwelcome side effects [1]. GdCl 3 is suggested to exert its anticoagulatory action by interfering in the generation of thrombin from prothrombin by factor Xa and by disturbing the proteolytic activation of factor XIII [11].…”
Section: Discussionmentioning
confidence: 99%