Cytotoxic and cytostatic effects of arecoline and sodium nitrite on human cells in vitro
β Scribed by K. K. Wary; R. N. Sharan
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- French
- Weight
- 488 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
Arecoline, an active alkaloid of Areca catechu L., and sodium nitrite, a food additive, are highly cytotoxic and cytostatic on the Hep 2 cell line when administered in an acidic environment (pH 4.2) in the presence of S-9 mixture. Hep 2 cells (10(6)) were treated with either 0.145, 0.725 or 1.449 mM sodium nitrite or 0.042, 0.085 or 0.339 mM arecoline or sodium nitrite (0.145 mM) plus varied concentrations of arecoline (0.042, 0.085 or 0.339 mM). Their effects were additive in nature. Hep 2 cells exposed to this combination showed reduced cell survival, and lower rates of DNA and protein syntheses. Involvement of N-nitroso derivatives of arecoline is suggested to explain the results. On the basis of these studies, we speculate that N-nitroso compounds derived from arecoline can (weakly) interact with DNA.
π SIMILAR VOLUMES
## METHODS. Two transitional cell carcinoma cell lines, MBT-2 and T24, were used in this study. The effects of fleroxacin and ciprofloxacin on cell proliferation were 1 Division of Urology, Minami Wakayama Nadetermined by counting the number of living cells and by colorimetric MTT assay.
We have demonstrated previously that high-dose methylprednisolone treatment induces differentiation and apoptosis of leukemic cells in patients with different morphological subtypes of acute myeloblastic leukemia (AML) in vivo. In the present study, we investigated the in vitro effects of high (10 -
## Abstract __In vivo__ experiments have shown that melanocytes are more sensitive than keratinocytes to the cytotoxic effects of sulfur mustard when it is applied topically to pig skin.1 It has been hypothesized that this is caused by the uncoupling of the melanogenic pathway by depletion of cellu
The specific effects of interferon alpha (IFNβ£), on the differentiation pathways of human osteogenic cells are not known. The aim of this study was to investigate possible effects of IFNβ£ on osteogenic development by investigating cell differentiation, colony formation (colony forming unit-fibroblas