1996
DOI: 10.1006/taap.1996.0209
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Effects of Lead on Growth Plate Chondrocyte Phenotype

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Cited by 49 publications
(41 citation statements)
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“…Our finding has also revealed that MSC has the ability to reduce residues of Pb in tissues (brain, liver, kidney, long bone, hair, heart, spleen, pancreas, longissimus muscle) as well as to increase the levels of serum GH in pigs as reported in other studies [18][19][20]. Therefore, it is concluded that MSC can be used for amelioration of Pb toxicity in animals and guarantee the safety of animal products.…”
Section: Discussionsupporting
confidence: 69%
“…Our finding has also revealed that MSC has the ability to reduce residues of Pb in tissues (brain, liver, kidney, long bone, hair, heart, spleen, pancreas, longissimus muscle) as well as to increase the levels of serum GH in pigs as reported in other studies [18][19][20]. Therefore, it is concluded that MSC can be used for amelioration of Pb toxicity in animals and guarantee the safety of animal products.…”
Section: Discussionsupporting
confidence: 69%
“…Lead (Pb), the heavy metal most widely studied in biological systems, has toxic effects on various organs including the skeleton (103)(104)(105). Bone is a major reservoir for ingested Pb (106), and delayed skeletal development occurs in children with prenatal exposure to Pb (107).…”
Section: The Influence Of Pathologic Stress On Chondrogenesis and Endmentioning
confidence: 99%
“…18 Lead affects chondrocytes and collagen maturation adversely. 4,5,[19][20][21][22][23] Collagen Type II (the main collagen in chondrocytes) and X, glycosaminoglycans in joint surfaces and transforming growth factor-β (suppressor of metalloproteinases) are shown to be the targets of lead toxicity. [19][20][21] Lead inhibits chondrocyte function by altering 1,25-dihydroxyvitamin D3, [12][13][14] parathyroid hormone-related peptide, transforming growth factor-β, and activator protein-1 and nuclear factor-κB signaling in chondrocytes.…”
Section: Discussionmentioning
confidence: 99%