[Blastomogenic action of low concentrations of nitrosodimethylamine, dimethylamine and nitrogen dioxide]

Voprosy Onkologii
|January 1, 1981
PubMed

Insights

Chronic inhalation of nitrosodimethylamine (NDMA) with dimethylamine (DMA) and nitrogen dioxide caused tumors in rats. The mixture enhanced NDMA

Area of Science:

  • Toxicology
  • Carcinogenesis
  • Environmental Health

Background:

  • Nitrosodimethylamine (NDMA) is a known carcinogen.
  • Dimethylamine (DMA) and nitrogen dioxide are environmental pollutants.
  • The combined effects of these substances on carcinogenicity are not fully understood.

Purpose of the Study:

  • To investigate the carcinogenic effects of chronic inhalation of NDMA, DMA, and nitrogen dioxide in rats.
  • To determine if DMA and nitrogen dioxide modify the carcinogenic activity of NDMA.
  • To assess sex-specific differences in tumor development.

Main Methods:

  • Albino non-bred rats were exposed to a mixture of NDMA, DMA, and nitrogen dioxide for one year.
  • NDMA concentrations varied within 0.66-0.0026 mg/m3.
  • Tumor development in various organs was monitored.

Main Results:

  • Continuous inhalation of the NDMA, DMA, and nitrogen dioxide mixture led to tumor development in the kidney, liver, lungs, and other sites.
  • The presence of DMA and nitrogen dioxide altered the carcinogenic effect of NDMA.
  • Male rats exposed to the mixture showed a higher blastogenic effect compared to those exposed to NDMA alone.
  • Female rats exposed to NDMA alone exhibited a lower tumor yield.

Conclusions:

  • Combined exposure to NDMA, DMA, and nitrogen dioxide is carcinogenic in rats.
  • DMA and nitrogen dioxide can modify the carcinogenic potential of NDMA.
  • Sex-specific differences exist in the response to these chemical exposures, with males showing a heightened carcinogenic response to the mixture.

Related Concept Videos

Carboxylic Acids to Methylesters: Alkylation using Diazomethane01:33

Carboxylic Acids to Methylesters: Alkylation using Diazomethane

Carboxylic acids react with diazomethane in an ether solvent via alkylation at the carboxylate oxygen atom to give methyl esters of the corresponding acid with excellent yields.
Preparation of Amines: Reduction of Oximes and Nitro Compounds01:29

Preparation of Amines: Reduction of Oximes and Nitro Compounds

Oximes can be reduced to primary amines using catalytic hydrogenation, hydride reduction, or sodium metal reduction. The reduction of aliphatic and aromatic nitro compounds to primary amines takes place by either catalytic hydrogenation or by using active metals like Fe, Zn, and Sn in the presence of an acid.
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview01:26

1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview

Nitrous acid and nitric acids are two types of acids containing nitrogen, among which nitrous acid is weaker than nitric acid. Nitrous acid with a pKa value of 3.37 ionizes in water to give a nitrite ion and the hydronium ion.
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by water loss...
2° Amines to N-Nitrosamines: Reaction with NaNO201:20

2° Amines to N-Nitrosamines: Reaction with NaNO2

Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion.
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism01:37

1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism

Nitrous acid is a relatively weak and unstable acid prepared in situ by the reaction of sodium nitrite and cold, dilute hydrochloric acid. In an acidic solution, the nitrous acid undergoes protonation when it loses water to form a nitrosonium ion—an electrophile. Nitrous acid reacts with primary amines to give diazonium salts. The reaction is called diazotization of primary amines.
Nitric Oxide Signaling Pathway01:28

Nitric Oxide Signaling Pathway

Nitric oxide (NO), an inorganic gas, acts as a potent second messenger in most animal and plant tissues. NO diffuses out of the cells that produce it and enters the neighboring cells to generate a downstream response. NO synthase (NOS) catalyzes NO production by the deamination of the amino acid arginine. There are three isoforms of NOS. Endothelial cells have endothelial NOS (eNOS), nerve and muscle cells have neuronal NOS (nNOS), and macrophages produce inducible NOS (iNOS) upon exposure to...