2011
DOI: 10.1016/j.bone.2010.12.007
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Nicotinic modulation of gene expression in osteoblast cells, MG-63

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Cited by 45 publications
(29 citation statements)
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“…Several cholinergic receptors, transporters, and enzymes were identified in bone forming osteoblasts as well as in bone resorbing osteoclasts [4,5,13]. Acetylcholine and the exogenous ligand nicotine are involved in proliferation of osteoprogenitors and their differentiation into active osteoblasts [13][14][15]. However, cholinergic markers in the non-neuronal system seemed to be reduced in osteoporosis.…”
Section: Discussionmentioning
confidence: 97%
“…Several cholinergic receptors, transporters, and enzymes were identified in bone forming osteoblasts as well as in bone resorbing osteoclasts [4,5,13]. Acetylcholine and the exogenous ligand nicotine are involved in proliferation of osteoprogenitors and their differentiation into active osteoblasts [13][14][15]. However, cholinergic markers in the non-neuronal system seemed to be reduced in osteoporosis.…”
Section: Discussionmentioning
confidence: 97%
“…Many studies have revealed that smoking, and nicotine in particular, has direct, detrimental effects on the health of bone and its ability to heal itself [11][12][13][14][15]. Cigarette smoking has been shown to interfere with bone formation, metabolism, and revascularization [14,15].…”
Section: Discussionmentioning
confidence: 99%
“…Nicotine exposure affects osteoblast proliferation, metabolism, extracellular matrix formation and growth factor signalling cascade including FGF-1, FGF-2, and RUNX2 [90,91]. Interestingly, using hepatic cell line HepaRG, it has been demonstrated that nicotine administration leads to dose-dependent reduction in NNK-induced DNA double strand break [92].…”
Section: In Vitro Studiesmentioning
confidence: 97%
“…Curcumin and its analog has modulatory activity on circulatory lipid profile in rats having nicotine-induced toxicity [106]. Melatonin, quercetin and hesperidin alleviated the effect of nicotine toxicity to liver [90][91][92][93][94]. Gender may also be a critical factor that could indicate the level of oxidative stress after nicotine exposure [107].…”
Section: In Vivo Studiesmentioning
confidence: 97%