Abstract:OBJECTIVE: By establishing a model of straight-leg swaddle of newborn rats and observing the experimental animals′ hips morphologically and pathologically, this study explored the changes of gross appearance of the acetabulum and the maturity of cartilage cells in the different regions of acetabular cartilage complex. METHODS: The legs and hips were fixed by adhesive tape for 10 days in the position of hip extension and adduction in 31 newborn Wistar rats (experimental group). The other 31 newborn rats without legs and hips treatment were used as the control group. After 10 days raising in the same condition, all the rats were sacrificed. The gross appearance, histological observations and VEGF and type X collagen immunohistochemistry were used for examining the acetabulum changes. RESULTS: A straight-leg swaddle model of newborn rats was established successfully. In the experimental group the acetabulum became shallow and small and surrounded by more soft tissues. There were 49 dislocated hips (49/54) in the experimental group and 2 hips dislocated (2/60) in the control group (P<0.01). Fake acetabulum appeared in the experimental group. In the control group, the shape of the acetabulum was normol, and no fake acetabulum was found. The safranin O-fast green staining showed that the orange-red cartilage in the experimental group was wider than the control group. Immunohistochemistry observations showed VEGF and type X collagen immunoreactivities in the hypertrophic layer of the acetabular cartilage complex in the experimental group were lower than those in the control group. The percentages of VEGF positive and type X collagen positive cells in the iliac hypertrophic layer of the acetabular articular cartilage were significantly higher than those in the ischiadic ramus and the pubic branch in the experimental group. CONCLUSIONS: VEGF and type X collagen immunoreactivities in acetabular cartilage cells decrease in a straight-leg swaddle model of newborn rats. This suggests that this position might lead to dysmaturity of the acetabular cartilage cells and affect the development of the acetabulum.[Chin J Contemp Pediatr, 2009, 11 (10):836-840]
ZHAO Xiao-Ming,WANG En-Bo,LI Jian-Jun et al. Developmental changes of acetabular cartilage complex: an experimental study of a straight-leg swaddle model of newborn rats[J]. CJCP, 2009, 11(10): 836-840.
[1]Kutlu A, Memik R, Mutlu M, Kutlu R, Arslan A. Congenital dislocation of the hip and its relation to swaddling used in Turkey[J]. J Pediatr Orhop, 1992, 12(5):598-602.
[2]Kremli MK, Alshahid AH, Khoshhal KI, Zamzam MM. The pattern of developmental dysplasia of the hip[J]. Saudi Med J, 2003, 24(10):1118-1120.
[3]Connolly P, Weinstein SL. The natural history of acetabular development in developmental dysplasia of the hip[J] . Acta Orthop Traumatol Turc, 2007, 41(Suppl 1):1-5.
[4]Cashin M, Uhthoff H, O′Neill M, Beaulé PE. Embryology of the acetabular labral-chondral complex[J]. J Bone Joint Surg Br, 2008, 90(8):1019-1024.
[5]Peng H, Usas A, Olshanski A, Ho AM, Gearhart B, Cooper GM, et al. VEGF improves, whereas sFlt1 inhibits, BMP2-induced bone formation and bone healing through modulation of angiogenesis[J]. J Bone Miner Res, 2005, 20(11):2017-2027.
[6]Higashikawa A, Kawaguchi H, Nakamura K, Chung U. Interactions of chondrocytes and osteoblasts during endochondral bone formation[J]. Clin Calcium, 2006, 16(5):829-836.
[7]Ishimaru J, Handa Y, Kurita K, Goss AN . The effect of occlusal loss on normal and pathological temporomandibular joints: an animal study[J]. J Craniomaxillofac Surg, 1994, 22(2):95-102.
[8]Herring JA. Developmental displysia of the hip[M].//Herring JA. Tachdjian′s Pediatric Orthopaedics. 3rd ed. Philadelphia:W.B.Saunders Company, 2002, 513-517.
[9]Ponseti IV. Growth and development of the acetabulum in the normal child. Anatomical, histological, and roentgenographic studies[J]. J Bone Joint Surg Am, 1978, 60(5):575-585.
[10]O′Hara JN. Congenital dislocation of the hip: acetabular deficiency in adolescence (absence of the lateral acetabular epiphysis) after limbectomy in infancy[J]. J Pediatr Orthop, 1989, 9(6):640-648.
[11]Bluteau G, Julien M, Magne D, Mallein-Gerin F, Weiss P, Daculsi G, et al. VEGF and VEGF receptor are differentially expressed in chondrocytes[J]. Bone, 2007, 40(3):568-576.
[13]Ali AM, Sharawy M. An immunohistochemical study of the effects of surgical induction of anterior disc displacement in the rabbit craniomandibular joint on type Ⅰ and type Ⅱ collagens[J].Archs Oral Biol, 1995, 40(6):473-480.
[14]Christesen LV, Ziebert GJ . Effects of experimental loss of teeth on the temporomandibular joint[J]. J Oral Rehabil, 1986, 13(6):587-598.
[15]Sweeney E, Campbell M, Watkins K, Hunter CA, Jacenko O. Altered endochondral ossification in collagen X mouse models leads to impaired immune responses[J]. Dev Dyn, 2008, 237(10):2693-2704.
[16]Kirsch T, vonder Mark K. Ca2+ binding properties of type X collagen[J]. FEBS Lett, 1991, 294(1-2):149-152.
[17]Kirsch T, Ishikawa Y, Mwale F, Wuthier RE. Roles of the nucleational core complex and collagens (types II and X) in calcification of growth plate cartilage matrix vesicles[J].J Biol Chem, 1994, 269(31):20103-20109.
[18]Klisic PJ. Congenital dislocation of the hip—a misleading term:brief report[J]. J Bone Joint Surg, 1989, 71(1):136.
[19]Smith WS, Ireton RJ, Coleman CR. Sequelae of experimental dislocation of a weight-bearing ball and socket joint in a young growing animal[J]. J Bone Joint Surg Am, 1958, 40(5):1121-1127.
[20]Harrison TJ. The influence of the femoral head on pelvic growth and acetabular form in the rat[J]. J Anat, 1961, 95:12-24.