The responses of hepatic monooxygenases of guinea pig to cadmium and nickel


ISCAN M., COBAN T., EKE B., ISCAN M.

Biological Trace Element Research, vol.38, no.2, pp.129-137, 1993 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 38 Issue: 2
  • Publication Date: 1993
  • Doi Number: 10.1007/bf02784049
  • Journal Name: Biological Trace Element Research
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.129-137
  • Keywords: CADMIUM, NICKEL, COMBINED TREATMENT, HEPATIC MONOOXYGENASES, GUINEA PIG, LIPID PEROXIDATION, LIVER, SYSTEM, RAT, STIMULATION, METABOLISM, ISOZYMES, ENZYMES, INVITRO, HEME
  • Ankara University Affiliated: Yes

Abstract

When Cd (3.58 mg CdCl 2 ·H 2 O/kg, ip) was administered to male guinea pigs 72 h prior to sacrifice, the metal significantly inhibited the aniline 4-hydroxylase (AH) (16%), ethylmorphone N-demethylase (EMND) (26%), and aminopyrine N-demethylase (AMND) (18%) activities and cytochrome P-450 (12%) and cytochrome b 5 (10%) levels. Cd did not alter the hepatic microsomal heme level. Cd, however, significantly increased the hepatic microsomal p-nitroanisole O-demethylase (p-NAOD) (53%) activity. When Ni (59.5 mg NiCl 2 ·6H 2 O/kg, sc) was administered to the guinea pigs 16 h prior to sacrifice, the metal significantly depressed AH (49%), p-NAOD (66%), EMND (47%), and AMND (37%) activities, and cytochrome P-450 (15%), cytochrome b 5 (24%), and microsomal heme (28%) levels. For the combined treatment, animals received the single dose of Ni 56 h after the single dose of Cd and then were killed 16 h later. In these animals, significant inhibitions were noted in AH (51%), EMND (47%), and AMND (30%) activities, and cytochrome P-450 (15%), cytochrome b 5 (26%), and microsomal heme (30%) compared to those of controls. In the case of p-NAOD activity, the influence was in favor of Ni, i.e, the inhibition was about 61% by the combined treatment. These results reveal that: 1. The response of all substrates of hepatic monooxygenases to Cd are not the same, possibly indicating differential regulation of cytochrome P-450 isozymes by Cd; 2. The inhibitory effect of Ni on hepatic monooxygenases is more profound than that of Cd; and 3. The combination of Cd and Ni does not have a synergistic effect of hepatic monooxygenases of the guinea pig. © 1993 Humana Press Inc.