Literature DB >> 24254327

The fate of Cd, Cu, Ca, Zn, and Fe in rat during the recovery period following cessation of repeated exposure to Cd.

E Komsta-Szumska1, M Czuba.   

Abstract

Cadmium was administered subcutaneously to male Wistar rats, 0.1 mL/rat in 0.9% saline 3 times a wk for 4 wk at 3 mg Cd/kg. Saline was administered to control animals in an equivalent manner, without Cd. After the end of the dosing period, the distribution and excretion of Cd, Cu, Ca, Zn, and Fe were observed in some organs and excreta for 35 d (1, 7, 14, 21, 28, and 35 d). Cadmium dosing caused significant disturbances in the metabolism of Zn, Cu, Fe, and Ca, especially during the recovery period. Growth in Cd-dosed animals did not accelerate, even after 5 wk of recovery. There was evidence of mobilization of some elements among organs. Accumulation of Cd occurred in liver, kidney, and spleen during dosing, and during the recovery period it was retained in kidney and testes (for 2 wk) and cleared steadily in liver and RBC (for 5 wk), but increased in spleen (first 3 wk). The pattern of Cd excretion was closely associated with the binding of Cd with metallothioneins in kidney and liver for the first 21 and 7 d, respectively. This was associated with the excretion of Cd-metallothioneins (Cd-MT) in urine from d 1 to 21 during recovery. Cadmium caused higher Ca accumulations in testes and liver, which were probably associated with the lesions observed in these organs. Significant increases of Cu (in kidney d 7) and Fe (in liver) were observed during recovery. Furthermore, significant reductions of Cu and Fe were found in plasma, spleen, and RBC (after 5 wk) and kidney, spleen, and testes (on d 7), and blood (after 5 wk).

Entities:  

Year:  1986        PMID: 24254327     DOI: 10.1007/BF02795318

Source DB:  PubMed          Journal:  Biol Trace Elem Res        ISSN: 0163-4984            Impact factor:   3.738


  23 in total

1.  Toxicity and distribution of cadmium administered to rats at sublethal doses.

Authors:  F N Kotsonis; C D Klaassen
Journal:  Toxicol Appl Pharmacol       Date:  1977-09       Impact factor: 4.219

2.  Influence of dietary pyridoxine on cadmium toxicity in rats.

Authors:  H D Stowe; R A Goyer; P Medley; M Cates
Journal:  Arch Environ Health       Date:  1974-04

3.  Cadmium accumulation in rat organs after extended oral administration with low concentrations of cadmium oxide.

Authors:  H J Weigel; H J Jäger; I Elmadfa
Journal:  Arch Environ Contam Toxicol       Date:  1984-05       Impact factor: 2.804

4.  Effect of diet on urinary and fecal excretion of cadmium, copper, and zinc from rats preaccumulated heavily with cadmium.

Authors:  K T Suzuki; E Miyamoto; Y Tanaka; R Kawamura; M Yamamura
Journal:  Arch Environ Contam Toxicol       Date:  1984-09       Impact factor: 2.804

5.  Serum proteins in cadmium poisoned rabbits: with special reference to hemolytic anemia.

Authors:  B Axelsson; M Piscator
Journal:  Arch Environ Health       Date:  1966-03

6.  The effects of sodium chromate and carbon tetrachloride on the urinary excretion and tissue distribution of cadmium in cadmium-pretreated rats.

Authors:  A M Bernard; R R Lauwerys
Journal:  Toxicol Appl Pharmacol       Date:  1981-01       Impact factor: 4.219

7.  The tissue disposition and urinary excretion of cadmium, zinc, copper and iron, following repeated parenteral administration of cadmium to rats.

Authors:  F W Bonner; L J King; D V Parke
Journal:  Chem Biol Interact       Date:  1979-10       Impact factor: 5.192

8.  Extent of cadmium accumulation and its effect on essential metals in liver, kidney, and body fluids.

Authors:  K T Suzuki; K Yaguchi; R Ohnuki; M Nishikawa; Y K Yamada
Journal:  J Toxicol Environ Health       Date:  1983 Apr-Jun

9.  Excessive hepatic accumulation of intracellular Ca2+ in chlordecone potentiated CCl4 toxicity.

Authors:  A K Agarwal; H M Mehendale
Journal:  Toxicology       Date:  1984-02-14       Impact factor: 4.221

10.  Effects of subcutaneous and oral cadmium on iron metabolism: role of ceruloplasmin and metallothionein.

Authors:  N Sugawara; C Sugawara; H Miyake
Journal:  Arch Toxicol       Date:  1984-11       Impact factor: 5.153

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.