2000
DOI: 10.1002/1097-0274(200009)38:3<340::aid-ajim15>3.0.co;2-s
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Effects of four inorganic lead compounds on the proliferation and junctional coupling of cultured REL liver cells

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Cited by 12 publications
(5 citation statements)
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“…For most heavy metals, there have been reports which indicate that the bioavailability of a metal and, in consequence, its toxic effect, is affected by its physicochemical form and the resulting solubility in water [17,18,19]. The results indicated that solubility in water was not the main factor which affected toxicity of cadmium compounds.…”
Section: Discussionmentioning
confidence: 99%
“…For most heavy metals, there have been reports which indicate that the bioavailability of a metal and, in consequence, its toxic effect, is affected by its physicochemical form and the resulting solubility in water [17,18,19]. The results indicated that solubility in water was not the main factor which affected toxicity of cadmium compounds.…”
Section: Discussionmentioning
confidence: 99%
“…18,24 However, these highly localized and short-term approaches cannot ensure actual biocompatibility over long-term periods, with genotoxic, metabolic, and clinical systems. [26][27][28][29][30] First, generally, heavy metal ion uptake-related symptoms do not occur directly or rapidly during a temporary exposure. 26,[31][32][33][34][35] Second, cell proliferation/adhesion are not seriously affected by surficial compositions, other than surficial topographies.…”
Section: Apl Mater 5 074102 (2017)mentioning
confidence: 99%
“…[21][22][23][26][27][28][29][30]72,73,78 To further directly inspect the chronological/clinical effects of bioimplanted piezoceramics, we are currently conducting biochemistry studies and long-term epidemiologic investigations using canine/porcine models.…”
Section: Apl Mater 5 074102 (2017)mentioning
confidence: 99%
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“…Liver tissue is the largest repository (33%) of lead among the soft tissues (Agency for Toxic Substances and Disease Registry, 2007). Several lines of evidence suggest that lead mediates hepatotoxicity through various mechanisms, including effects on hepatic drug-metabolizing enzymes, hepatic necrosis (Sivaprasad et al, 2004;Berrahal et al, 2009), abnormal liver function (Al-Neamy et al, 2001) and liver cell proliferation through the enhanced expression of tumor necrosis factor-alpha (TNF-a; Kubo et al, 1996;Shinozuka et al, 1996;Apostoli et al, 2000). Lead also mediates hepatotoxicity through the induction of cellular oxidative stress (Aykin-Burns et al, 2003;Sivaprasad et al, 2004;Berrahal et al, 2009).…”
Section: Introductionmentioning
confidence: 99%