Ovariectomized rats as a model of postmenopausal osteoarthritis: validation and application

Pernille Høegh-Andersen; László B Tankó; Thomas L Andersen; Carina V Lundberg; John A Mo; Anne-Marie Heegaard; Jean-Marie Delaissé; Stephan Christgau

doi:10.1186/ar1152

Ovariectomized rats as a model of postmenopausal osteoarthritis: validation and application

Pernille Høegh-Andersen, László B Tankó, Thomas L Andersen, Carina V Lundberg, John A Mo, Anne-Marie Heegaard, Jean-Marie Delaissé, Stephan Christgau

189 Citations (Scopus)

Abstract

We aimed to assess the effect of ovariectomy on cartilage turnover and degradation, to evaluate whether ovariectomized (OVX) rats could form an experimental model of postmenopausal osteoarthritis. The effect of ovariectomy on cartilage was studied using two cohorts of female Sprague-Dawley rats, aged 5 and 7 months. In a third cohort, the effect of exogenous estrogen and a selective estrogen receptor modulator was analyzed. Knee joints were assessed by histological analysis of the articular cartilage after 9 weeks. Cartilage turnover was measured in urine by an immunoassay specific for collagen type II degradation products (CTX-II), and bone resorption was quantified in serum using an assay for bone collagen type I fragments (CTX-I). Surface erosion in the cartilage of the knee was more severe in OVX rats than in sham-operated animals, particularly in the 7-month-old cohort (P = 0.008). Ovariectomy also significant increased CTX-I and CTX-II. Both the absolute levels of CTX-II and the relative changes from baseline seen at week 4 correlated strongly with the severity of cartilage surface erosion at termination (r = 0.74, P <0.01). Both estrogen and the selective estrogen receptor modulator inhibited the ovariectomy-induced acceleration of cartilage and bone turnover and significantly suppressed cartilage degradation and erosion seen in vehicle-treated OVX rats. The study indicates that estrogen deficiency accelerates cartilage turnover and increases cartilage surface erosion. OVX rats provide a useful experimental model for the evaluation of the chondroprotective effects of estrogens and estrogen-like substances and the model may be an in vivo representation of osteoarthritis in postmenopausal women.

Original language	English
Journal	Arthritis Research & Therapy
Volume	6
Issue number	2
Pages (from-to)	R169-80
ISSN	1478-6362
DOIs	https://doi.org/10.1186/ar1152
Publication status	Published - 2004
Externally published	Yes

Keywords

Aging
Animals
Biological Markers
Bone Resorption
Bone and Bones
Cartilage
Collagen Type I
Collagen Type II
Disease Models, Animal
Estrogens
Female
Organ Size
Osteoarthritis
Ovariectomy
Postmenopause
Rats
Rats, Sprague-Dawley
Selective Estrogen Receptor Modulators
Uterus

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10.1186/ar1152

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title = "Ovariectomized rats as a model of postmenopausal osteoarthritis: validation and application",

abstract = "We aimed to assess the effect of ovariectomy on cartilage turnover and degradation, to evaluate whether ovariectomized (OVX) rats could form an experimental model of postmenopausal osteoarthritis. The effect of ovariectomy on cartilage was studied using two cohorts of female Sprague-Dawley rats, aged 5 and 7 months. In a third cohort, the effect of exogenous estrogen and a selective estrogen receptor modulator was analyzed. Knee joints were assessed by histological analysis of the articular cartilage after 9 weeks. Cartilage turnover was measured in urine by an immunoassay specific for collagen type II degradation products (CTX-II), and bone resorption was quantified in serum using an assay for bone collagen type I fragments (CTX-I). Surface erosion in the cartilage of the knee was more severe in OVX rats than in sham-operated animals, particularly in the 7-month-old cohort (P = 0.008). Ovariectomy also significant increased CTX-I and CTX-II. Both the absolute levels of CTX-II and the relative changes from baseline seen at week 4 correlated strongly with the severity of cartilage surface erosion at termination (r = 0.74, P <0.01). Both estrogen and the selective estrogen receptor modulator inhibited the ovariectomy-induced acceleration of cartilage and bone turnover and significantly suppressed cartilage degradation and erosion seen in vehicle-treated OVX rats. The study indicates that estrogen deficiency accelerates cartilage turnover and increases cartilage surface erosion. OVX rats provide a useful experimental model for the evaluation of the chondroprotective effects of estrogens and estrogen-like substances and the model may be an in vivo representation of osteoarthritis in postmenopausal women.",

keywords = "Aging, Animals, Biological Markers, Bone Resorption, Bone and Bones, Cartilage, Collagen Type I, Collagen Type II, Disease Models, Animal, Estrogens, Female, Organ Size, Osteoarthritis, Ovariectomy, Postmenopause, Rats, Rats, Sprague-Dawley, Selective Estrogen Receptor Modulators, Uterus",

author = "Pernille H{\o}egh-Andersen and Tank{\'o}, {L{\'a}szl{\'o} B} and Andersen, {Thomas L} and Lundberg, {Carina V} and Mo, {John A} and Anne-Marie Heegaard and Jean-Marie Delaiss{\'e} and Stephan Christgau",

year = "2004",

doi = "10.1186/ar1152",

language = "English",

volume = "6",

pages = "R169--80",

journal = "Arthritis Research & Therapy",

issn = "1478-6354",

publisher = "BioMed Central",

number = "2",

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TY - JOUR

T1 - Ovariectomized rats as a model of postmenopausal osteoarthritis

T2 - validation and application

AU - Høegh-Andersen, Pernille

AU - Tankó, László B

AU - Andersen, Thomas L

AU - Lundberg, Carina V

AU - Mo, John A

AU - Heegaard, Anne-Marie

AU - Delaissé, Jean-Marie

AU - Christgau, Stephan

PY - 2004

Y1 - 2004

N2 - We aimed to assess the effect of ovariectomy on cartilage turnover and degradation, to evaluate whether ovariectomized (OVX) rats could form an experimental model of postmenopausal osteoarthritis. The effect of ovariectomy on cartilage was studied using two cohorts of female Sprague-Dawley rats, aged 5 and 7 months. In a third cohort, the effect of exogenous estrogen and a selective estrogen receptor modulator was analyzed. Knee joints were assessed by histological analysis of the articular cartilage after 9 weeks. Cartilage turnover was measured in urine by an immunoassay specific for collagen type II degradation products (CTX-II), and bone resorption was quantified in serum using an assay for bone collagen type I fragments (CTX-I). Surface erosion in the cartilage of the knee was more severe in OVX rats than in sham-operated animals, particularly in the 7-month-old cohort (P = 0.008). Ovariectomy also significant increased CTX-I and CTX-II. Both the absolute levels of CTX-II and the relative changes from baseline seen at week 4 correlated strongly with the severity of cartilage surface erosion at termination (r = 0.74, P <0.01). Both estrogen and the selective estrogen receptor modulator inhibited the ovariectomy-induced acceleration of cartilage and bone turnover and significantly suppressed cartilage degradation and erosion seen in vehicle-treated OVX rats. The study indicates that estrogen deficiency accelerates cartilage turnover and increases cartilage surface erosion. OVX rats provide a useful experimental model for the evaluation of the chondroprotective effects of estrogens and estrogen-like substances and the model may be an in vivo representation of osteoarthritis in postmenopausal women.

AB - We aimed to assess the effect of ovariectomy on cartilage turnover and degradation, to evaluate whether ovariectomized (OVX) rats could form an experimental model of postmenopausal osteoarthritis. The effect of ovariectomy on cartilage was studied using two cohorts of female Sprague-Dawley rats, aged 5 and 7 months. In a third cohort, the effect of exogenous estrogen and a selective estrogen receptor modulator was analyzed. Knee joints were assessed by histological analysis of the articular cartilage after 9 weeks. Cartilage turnover was measured in urine by an immunoassay specific for collagen type II degradation products (CTX-II), and bone resorption was quantified in serum using an assay for bone collagen type I fragments (CTX-I). Surface erosion in the cartilage of the knee was more severe in OVX rats than in sham-operated animals, particularly in the 7-month-old cohort (P = 0.008). Ovariectomy also significant increased CTX-I and CTX-II. Both the absolute levels of CTX-II and the relative changes from baseline seen at week 4 correlated strongly with the severity of cartilage surface erosion at termination (r = 0.74, P <0.01). Both estrogen and the selective estrogen receptor modulator inhibited the ovariectomy-induced acceleration of cartilage and bone turnover and significantly suppressed cartilage degradation and erosion seen in vehicle-treated OVX rats. The study indicates that estrogen deficiency accelerates cartilage turnover and increases cartilage surface erosion. OVX rats provide a useful experimental model for the evaluation of the chondroprotective effects of estrogens and estrogen-like substances and the model may be an in vivo representation of osteoarthritis in postmenopausal women.

KW - Aging

KW - Animals

KW - Biological Markers

KW - Bone Resorption

KW - Bone and Bones

KW - Cartilage

KW - Collagen Type I

KW - Collagen Type II

KW - Disease Models, Animal

KW - Estrogens

KW - Female

KW - Organ Size

KW - Osteoarthritis

KW - Ovariectomy

KW - Postmenopause

KW - Rats

KW - Rats, Sprague-Dawley

KW - Selective Estrogen Receptor Modulators

KW - Uterus

U2 - 10.1186/ar1152

DO - 10.1186/ar1152

M3 - Journal article

C2 - 15059281

SN - 1478-6354

VL - 6

SP - R169-80

JO - Arthritis Research & Therapy

JF - Arthritis Research & Therapy

IS - 2

ER -

Ovariectomized rats as a model of postmenopausal osteoarthritis: validation and application

Abstract

Keywords

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