Chemical reactivity, cytotoxicity, and mutagenicity of chloropropanones.

Abstract:

:Studies were conducted to assess the in vitro toxicity of three chloropropanones: monochloropropanone (MCP), 1,1-dichloropropanone (1,1-DCP), and 1,3-dichloropropanone (1,3-DCP). Chloropropanones reacted directly with reduced glutathione (GSH) in sodium phosphate buffer at pH 7.4. All chloropropanones were cytotoxic to suspensions of male rat hepatocytes in a concentration range of 0.5-10 mM. Cytotoxicity was preceded by rapid decline in cellular GSH levels. Mutagenic potencies among the chloropropanones in Salmonella typhimurium bacteria differed greatly. 1,3-DCP was mutagenic in the nanomole range, 1,1-DCP was weakly mutagenic in the micromole range, and MCP was not mutagenic. Mutagenicity of the dichloropropanones was evident without metabolic activation. These results suggest that the three chloropropanones may, in part, be directly cytotoxic but only 1,3-DCP and 1,1-DCP are directly mutagenic.

journal_name

Toxicol Appl Pharmacol

authors

Merrick BA,Smallwood CL,Meier JR,McKean DL,Kaylor WH,Condie LW

doi

10.1016/0041-008x(87)90192-x

subject

Has Abstract

pub_date

1987-10-01 00:00:00

pages

46-54

issue

1

eissn

0041-008X

issn

1096-0333

journal_volume

91

pub_type

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