RECOVERY FROM PAMIDRONATE (APD) - A 2-YEAR STUDY IN THE DOG

被引:10
作者
GRYNPAS, MD
KASRA, M
DUMITRIU, M
NESPECA, R
VERY, JM
MERTZ, BP
机构
[1] UNIV TORONTO,TORONTO M5G 1X5,ON,CANADA
[2] CIBA GEIGY AG,CH-4002 BASEL,SWITZERLAND
关键词
BISPHOSPHONATE; BONE MINERALIZATION; STRUCTURE; MECHANICAL PROPERTIES; DOG; RECOVERY;
D O I
10.1007/BF00310408
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The goal of this study was to find out if bone can recover after long-term administration of bisphosphonate. Disodium pamidronate (APD) was given orally by gavage to mature beagle dogs at doses of 0, 2.5, 12.5, and 25 mg/kg/day for 1 year (0.1% concentration) and the animals were allowed to recover for another year. At sacrifice, the os ilium was used to determine bone mineralization profile and, subsequently, each density fraction was analyzed chemically. The ribs were used to determine the lattice parameters and the size of the apatite crystals of bone. The sternum was used to determine selected morphometric parameters using image analysis of specimen X-ray films and, subsequently, to determine bone mechanical properties using a 3-point bending technique. We found that the 12.5 and 25 mg/kg/day doses exhibit a significant shift towards greater mineralization versus control, whereas the lower dose (2.5 mg/kg/day) was indistinguishable from the controls. The lattice parameters and crystal size of bone apatite remained unchanged. The image analysis shows a dose-related increase in trabecular volume and thickness. The connectivity increased with dose but the anisotropy of bone remained unchanged. Both the elastic modulus and the maximum stress of bone remain unaffected by APD. We conclude that when dogs are treated with APD for 1 year, their bones can reestablish their physical-chemical characteristics (mineralization profile, chemistry, and crystal size/strain) after 1 year of recovery, provided that the treatment dose is 2.5 mg/kg/day. In addition, the mechanical properties of the bone remained unaffected and the gains in trabecular volume and thickness are maintained.
引用
收藏
页码:288 / 294
页数:7
相关论文
共 21 条
[1]   EVALUATION OF THE BECKMAN SYNCHRON CX4 CLINICAL-CHEMISTRY ANALYZER IN A HOSPITAL LABORATORY [J].
AMBUS, T ;
KOROGYI, N ;
DECAMPOS, F ;
GROOM, B ;
INNANEN, VT .
JOURNAL OF CLINICAL LABORATORY ANALYSIS, 1990, 4 (02) :120-125
[2]   X-RAY-DIFFRACTION STUDIES OF THE CRYSTALLINITY OF BONE-MINERAL IN NEWLY SYNTHESIZED AND DENSITY FRACTIONATED BONE [J].
BONAR, LC ;
ROUFOSSE, AH ;
SABINE, WK ;
GRYNPAS, MD ;
GLIMCHER, MJ .
CALCIFIED TISSUE INTERNATIONAL, 1983, 35 (02) :202-209
[3]   RATIONALE FOR DIPHOSPHONATE THERAPY IN HYPERCALCEMIA OF MALIGNANCY - INTRODUCTION [J].
CANFIELD, RE .
AMERICAN JOURNAL OF MEDICINE, 1987, 82 (2A) :1-5
[4]  
CHAPPARD D, 1991, J BONE MINER RES, V6, P673
[5]  
EINHORN T, 1990, J BONE MINER RES, V5, P597
[6]   DETERMINATION OF CARBONATE CARBON IN GEOLOGICAL-MATERIALS BY COULOMETRIC TITRATION [J].
ENGLEMAN, EE ;
JACKSON, LL ;
NORTON, DR .
CHEMICAL GEOLOGY, 1985, 53 (1-2) :125-128
[7]   BIOMECHANICAL EFFECTS OF THE FULL RANGE OF USEFUL DOSES OF (3-AMINO-1-HYDROXYPROPYLIDENE)-1,1-BISPHOSPHONATE (APD) ON FEMUR DIAPHYSES AND CORTICAL BONE TISSUE IN RATS [J].
FERRETTI, JL ;
COINTRY, G ;
CAPOZZA, R ;
MONTUORI, E ;
ROLDAN, E ;
LLORET, AP .
BONE AND MINERAL, 1990, 11 (01) :111-122
[8]  
Francis M.D., 1983, P55
[9]  
FRIJLINK WB, 1979, LANCET, V1, P799
[10]  
Fromm G A, 1991, Osteoporos Int, V1, P129, DOI 10.1007/BF01625440