Literature DB >> 7246426

Toxicokinetics of nickel in rats after intratracheal administration of a soluble and insoluble form.

J C English, R D Parker, R P Sharma, S G Oberg.   

Abstract

Ninety day laboratory studies were performed to determine the whole body distribution of two chemical forms of nickel in female Wistar rats. A single injections of 15 microCi of 63Ni, either NiCl2 as a solution or NiO as a suspension, 100 nmoles in each case, was administered intratracheally. Rats were sacrificed at post-exposure intervals of 0.5, 2, and 8 hours, 1, 3, 7, 15, 30, 60 and 90 days, and major organs and tissues were analyzed for 63Ni by liquid scintillation counting technique. The soluble NiCl2 was readily distributed throughout the body, and rapidly cleared from the tissues. The insoluble NiO was distributed slowly to other organs from pulmonary tissues. The rate of decline of 63Ni from various organs in the case of NiO was similar to that of NiCl2, with notable exceptions being the lung and associated lymph nodes. After NiO administration, these organs showed a high retention of nickel after 90 days. Results indicated that Ni in soluble form was rapidly absorbed from the site of deposition following pulmonary exposure, whereas, Ni in its oxide or insoluble form was retained in lungs and related lymphatics for a considerable period. The amount of Ni in other organs following NiO exposure, though initially low in all tissues, declined in a fashion similar to organs following NiCl2 exposure. This suggests that NiO was possibly converted to a soluble form of Ni before it was translocated from lungs to other organs, and that low environmental levels of insoluble forms of nickel, which persist in the lung and lymph nodes, do have the potential for assimilation in these tissues.

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Year:  1981        PMID: 7246426     DOI: 10.1080/15298668191420125

Source DB:  PubMed          Journal:  Am Ind Hyg Assoc J        ISSN: 0002-8894


  5 in total

1.  Kinetics of nickel binding in hepatic and renal cytosol of(63)NiCl 2-treated rats.

Authors:  J R Behari; P P Dwivedi; M Misra; R C Srivastava
Journal:  Biol Trace Elem Res       Date:  1984-12       Impact factor: 3.738

2.  Sex and age mortality responses in zinc acetate-treated mice.

Authors:  G R Hogan; B S Cole; J M Lovelace
Journal:  Bull Environ Contam Toxicol       Date:  1987-07       Impact factor: 2.151

3.  Nickel acetate-induced mortality in mice of different ages.

Authors:  G R Hogan
Journal:  Bull Environ Contam Toxicol       Date:  1985-03       Impact factor: 2.151

4.  Comparison of single or multiple intratracheal administration for pulmonary toxic responses of nickel oxide nanoparticles in rats.

Authors:  Hideki Senoh; Hirokazu Kano; Masaaki Suzuki; Makoto Ohnishi; Hitomi Kondo; Kenji Takanobu; Yumi Umeda; Shigetoshi Aiso; Shoji Fukushima
Journal:  J Occup Health       Date:  2016-12-15       Impact factor: 2.708

5.  Phytogenic Generation of NiO Nanoparticles Using Stevia Leaf Extract and Evaluation of Their In-Vitro Antioxidant and Antimicrobial Properties.

Authors:  Saiganesh Srihasam; Krishnan Thyagarajan; Mallikarjuna Korivi; Veeranjaneya Reddy Lebaka; Siva Pratap Reddy Mallem
Journal:  Biomolecules       Date:  2020-01-06
  5 in total

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