Published November 20, 2008 | Version v1
Journal article

In utero and lactational exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) affects bone tissue in rhesus monkeys

  • 1. Institute of Environmental Medicine, Karolinska Institutet, Nobels vaeg 13, Box 210, S-17177 Stockholm (Sweden)
  • 2. Department of Surgical Sciences, Orthopaedics, Uppsala University (Sweden)
  • 3. Drug Safety Research Laboratories, Shin Nippon Biomedical Laboratories Ltd., Kagoshima 891-1394 (Japan)
  • 4. Department of Clinical Radiology, Faculty of Health Sciences, Hiroshima International University, Higashi-Hiroshima 724-0695 (Japan)
  • 5. Department of Pathology, Teikyo University School of Medicine, Tokyo 173-8606 (Japan)
  • 6. Department of Life Sciences, Graduate School of Arts and Sciences, University of Tokyo, Tokyo 173-8606 (Japan)

Description

Bone tissue is one of the target tissues for dioxins and dioxin-like compounds. Therefore, the aim of this study was to investigate effects of in utero and lactational exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), on bone tissue in rhesus monkey, the most human-like experimental model available. Pregnant rhesus monkeys (Macaca mulatta; age 4-10 years) were exposed to TCDD with a total dose of 40.5-42.0 or 405-420 ng/kg bodyweight by repeated subcutaneous injections starting at gestational day 20 and followed by injections every 30 days until 90 days after delivery. At a mean age of 7 years the offspring were sacrificed and the femur bone dissected. Results from peripheral Quantitative Computed Tomography (pQCT) analyses of the metaphyseal part of the femur bones in female offspring showed significant increases in trabecular bone mineral content (BMC; +84.6%, p < 0.05, F-value (F) = 5.9) in the low-dose treatment group compared with the controls. In the same animals, analysis of the mid-diaphyseal part revealed increases in total BMC (+21.3%, p < 0.05, F = 5.2) and cortical cross-sectional area (CSA; +16.4%, p < 0.01, F = 7.4) compared with the controls. In males, changes in biomechanical properties indicating more fragile bone were observed. Displacement at failure were significantly increased in the male low-dose group compared to the controls (+38.0%, p < 0.05, F = 11). The high dose of TCDD did not induce any significant changes in bone morphology. In conclusion, in utero and lactational low-dose, but not high-dose exposure to 2,3,7,8-TCDD induced disruption of bone tissue development in rhesus monkey, a result suggesting that similar effects might occur in humans also

Availability note (English)

Available from http://dx.doi.org/10.1016/j.tox.2008.09.005

Additional details

Identifiers

DOI
10.1016/j.tox.2008.09.005;
PII
S0300-483X(08)00430-7;

Publishing Information

Journal Title
Toxicology
Journal Volume
253
Journal Issue
1-3
Journal Page Range
p. 147-152
ISSN
0300-483X
CODEN
TXCYAC

Conference

Title
2008 annual congress of the british toxicology society
Dates
6-9 Apr 2008
Place
Guildford (United Kingdom)

INIS

Country of Publication
Ireland
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
40055587
Subject category
S60: APPLIED LIFE SCIENCES;
Resource subtype / Literary indicator
Conference
Descriptors DEI
COMPUTERIZED TOMOGRAPHY; DIOXIN; DOSES; FEMUR; MACACUS; MORPHOLOGY; SUBCUTANEOUS INJECTION; TOXICITY; TRABECULAR BONE
Descriptors DEC
ANIMAL TISSUES; ANIMALS; BODY; BONE TISSUES; CONNECTIVE TISSUE; DIAGNOSTIC TECHNIQUES; HETEROCYCLIC COMPOUNDS; INJECTION; INTAKE; MAMMALS; MONKEYS; ORGANIC COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; ORGANS; PRIMATES; SKELETON; TOMOGRAPHY; VERTEBRATES

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.