Effects of SO2 or NOx on toxic and genotoxic properties of chemical carcinogens. II. Short term In vitro studies

1988 ◽  
Vol 9 (7) ◽  
pp. 1247-1252 ◽  
Author(s):  
B.L. Pool ◽  
S. Brendler ◽  
R.G. Klein ◽  
S. Monarca ◽  
R. Pasquini ◽  
...  
2016 ◽  
pp. 142-149
Author(s):  
Paula A. Oliveira

The development of cancer associated with exposure to chemical carcinogens is a reality and existing knowledge of these cancers is based on epidemiological, in vivo, and in vitro studies. Chemical carcinogens are present virtually everywhere and humans can be exposed to these compounds in food, air, water, their environment, or their workplace. This chapter is concerned with the main types of exogenous chemical carcinogens, how they are classified and their modes of action, absorption, and metabolism, as well as the principal tests available for evaluating their carcinogenicity. Only exogenous chemicals are considered in this chapter, since exogenous chemical carcinogens may be the major contributors to human cancer.


1988 ◽  
Vol 9 (7) ◽  
pp. 1237-1246 ◽  
Author(s):  
B.L. Pool ◽  
I. Janowsky ◽  
P. Klein ◽  
R.G. Klein ◽  
P. Schmezer ◽  
...  

1988 ◽  
Vol 20 (4) ◽  
pp. 343-348 ◽  
Author(s):  
P.R. Subramanian ◽  
R. Kadirvel ◽  
K. Viswanathan ◽  
D. Chandrasekaran

Author(s):  
Paula A. Oliveira

The development of cancer associated with exposure to chemical carcinogens is a reality and existing knowledge of these cancers is based on epidemiological, in vivo, and in vitro studies. Chemical carcinogens are present virtually everywhere and humans can be exposed to these compounds in food, air, water, their environment, or their workplace. This chapter is concerned with the main types of exogenous chemical carcinogens, how they are classified and their modes of action, absorption, and metabolism, as well as the principal tests available for evaluating their carcinogenicity. Only exogenous chemicals are considered in this chapter, since exogenous chemical carcinogens may be the major contributors to human cancer.


Author(s):  
D.E. Loudy ◽  
J. Sprinkle-Cavallo ◽  
J.T. Yarrington ◽  
F.Y. Thompson ◽  
J.P. Gibson

Previous short term toxicological studies of one to two weeks duration have demonstrated that MDL 19,660 (5-(4-chlorophenyl)-2,4-dihydro-2,4-dimethyl-3Hl, 2,4-triazole-3-thione), an antidepressant drug, causes a dose-related thrombocytopenia in dogs. Platelet counts started to decline after two days of dosing with 30 mg/kg/day and continued to decrease to their lowest levels by 5-7 days. The loss in platelets was primarily of the small discoid subpopulation. In vitro studies have also indicated that MDL 19,660: does not spontaneously aggregate canine platelets and has moderate antiaggregating properties by inhibiting ADP-induced aggregation. The objectives of the present investigation of MDL 19,660 were to evaluate ultrastructurally long term effects on platelet internal architecture and changes in subpopulations of platelets and megakaryocytes.Nine male and nine female beagle dogs were divided equally into three groups and were administered orally 0, 15, or 30 mg/kg/day of MDL 19,660 for three months. Compared to a control platelet range of 353,000- 452,000/μl, a doserelated thrombocytopenia reached a maximum severity of an average of 135,000/μl for the 15 mg/kg/day dogs after two weeks and 81,000/μl for the 30 mg/kg/day dogs after one week.


2006 ◽  
Vol 15 (04) ◽  
pp. 245-257 ◽  
Author(s):  
H. J. Rolf ◽  
K. G. Wiese ◽  
H. Siggelkow ◽  
H. Schliephake ◽  
G. A. Bubernik

1976 ◽  
Vol 36 (01) ◽  
pp. 221-229 ◽  
Author(s):  
Charles A. Schiffer ◽  
Caroline L. Whitaker ◽  
Morton Schmukler ◽  
Joseph Aisner ◽  
Steven L. Hilbert

SummaryAlthough dimethyl sulfoxide (DMSO) has been used extensively as a cryopreservative for platelets there are few studies dealing with the effect of DMSO on platelet function. Using techniques similar to those employed in platelet cryopreservation platelets were incubated with final concentrations of 2-10% DMSO at 25° C. After exposure to 5 and 10% DMSO platelets remained discoid and electron micrographs revealed no structural abnormalities. There was no significant change in platelet count. In terms of injury to platelet membranes, there was no increased availability of platelet factor-3 or leakage of nucleotides, 5 hydroxytryptamine (5HT) or glycosidases with final DMSO concentrations of 2.5, 5 and 10% DMSO. Thrombin stimulated nucleotide and 5HT release was reduced by 10% DMSO. Impairment of thrombin induced glycosidase release was noted at lower DMSO concentrations and was dose related. Similarly, aggregation to ADP was progressively impaired at DMSO concentrations from 1-5% and was dose related. After the platelets exposed to DMSO were washed, however, aggregation and release returned to control values. Platelet aggregation by epinephrine was also inhibited by DMSO and this could not be corrected by washing the platelets. DMSO-plasma solutions are hypertonic but only minimal increases in platelet volume (at 10% DMSO) could be detected. Shrinkage of platelets was seen with hypertonic solutions of sodium chloride or sucrose suggesting that the rapid transmembrane passage of DMSO prevented significant shifts of water. These studies demonstrate that there are minimal irreversible alterations in in vitro platelet function after short-term exposure to DMSO.


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