Study of correlation between lead-induced cytotoxicity and nitric oxide production in PC12 cells
Sharifi, AM; Mousavi, SH; Bakhshayesh, M; Tehrani, FK; Mahmoudian, M; Oryan, SB
| HERO ID | 520669 |
|---|---|
| In Press | No |
| Year | 2005 |
| Title | Study of correlation between lead-induced cytotoxicity and nitric oxide production in PC12 cells |
| Authors | Sharifi, AM; Mousavi, SH; Bakhshayesh, M; Tehrani, FK; Mahmoudian, M; Oryan, SB |
| Journal | Toxicology Letters |
| Volume | 160 |
| Issue | 1 |
| Page Numbers | 43-48 |
| Abstract | Despite reduction in its exposure, lead remains a major health problem. The primary target of lead toxicity is the central nervous system. The cellular, intracellular and molecular mechanisms of lead neurotoxicity are numerous, such as induction of apoptosis and interfering with Ca2+ dependent enzyme like nitric oxide synthase (NOS). To investigate the cytotoxic effect of lead on rat pheochromocytoma (PC12) cells, as a suitable model for neuroscience study, and possible correlation between lead toxicity and nitric oxide (NO) production, this study was performed. The current results showed that lead could induce cytotoxicity as well as NO production in a dose dependent manner in PC12 cells after 24h. The cytotoxicity was positively correlated with increased NO, (nitrite and nitrate) production in these cells. L-NAME, a NOS inhibitor, treatment (2.5 mM) could reverse this cytotoxicity. It can be concluded that lead-induced cytotoxicity in PC12 cells could partly be mediated by higher NO production. (c) 2005 Elsevier Ireland Ltd. All rights reserved. |
| Doi | 10.1016/j.toxlet.2005.06.008 |
| Pmid | 16039808 |
| Wosid | WOS:000233341800005 |
| Is Certified Translation | No |
| Dupe Override | No |
| Comments | Source: Web of Science WOS:000233341800005 |
| Is Public | Yes |
| Language Text | English |
| Keyword | PC12; lead; nitric oxide; L-NAME; developing rat-brain; tyrosine-hydroxylase; in-vivo; neurotoxicity; apoptosis; toxicity; synthase; activation; growth; induction |
| Is Qa | No |
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