Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Periosteum”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 109 records · Page 6Linked to original sources

The radiographic and histologic appearance of controlled surgical manipulation of the equine periosteum.

This study documented the normal histologic features of the equine metacarpal and metatarsal periosteum and characterized its osteogenic response to surgical manipulation. Two periosteal flaps were elevated from the dorsomedial matacarpal and metatarsal diaphysis in each of three limbs of four yearling and four adult lightbreed horses. The superficial metacarpal cortex under the flap was resected with a bone chisel in one-half of the horses and was undisturbed in the remainder. One periosteal flap in each limb was excised and the other flap was replaced and secured by sutures. All limbs in the horses were radiographed at regular intervals postoperatively. Horses were killed either 30 or 120 days after surgery. Periosteal bone production occurred only at treatment sites of young horses treated by periosteal flap replacement and was limited to approximately 50% of these sites, as determined by radiography and microradiography. Cortical abrasion resulted in an increased incidence of bone production in the periosteum adjacent to the flap perimeter. The histologic features of the periosteum were similar to those reported in other species; young horses had active osteogenesis referable to appositional growth and adults had an inactive periosteum. Histologically, osteogenesis induced by surgery resembled accentuated appositional growth in both yearlings and adults. In the horse, the cambial (osteogenic) layer is included in sharply elevated periosteal flaps. It should be removed in surgical procedures where bone production is to be avoided, and preserved where osteogenesis is desired.

Animals↗

Differentiative ability of the tibial periosteum for the embryonic chick.

The claim that the hypertrophic cartilage of a transversely divided 9-day chick tibia is able to induce the differentiation of osteoblasts when placed against the fibrous periosteum of a second, intact, 9-day tibia in vitro, is refuted. Tibia from 7- and 9-day-old chick embryos were transversely sectioned though either the diaphysis or epiphysis and these diaphyseal and epiphyseal grafts were then placed in close association with the fibrous periostea of intact, host tibiae of the same or different ages, at either the diaphyseal or epiphyseal level. All of the sixteen possible combinations of paired tibiae were established in organ culture for 7 days on three types of culture media and two types of atmospheres. In response to the close contact established when diaphyseal grafts were used, the fibrous layer of the periosteum underwent hyperplasia to form fibroblasts at the contact site. Contact of the graft with the periosteum as not sufficient to allow osteoprogenitor cells to accumulate, to differentiate into osteoblasts, or to deposit osteoid. We concluded that the outer, fibrous layer of the periosteum is fibroblastic and not osteblastic.

Animals↗

Microscopic study of the rabbit mandibular periosteum and attached structures.

The structure of the mandibular periosteum in rabbits of different ages has been studied by different histological staining techniques and polarization microscopy. The periosteum consisted of two layers. From the inner, cellular layer the functional state could be determined. A reproducible pattern of resorptive and depository areas was found on the bony surface. In the outer, fibrous periosteal layer, collagenous and elastin fibers were running in distinct directions. The masticatory muscles appeared to be attached directly endomysially or indirectly endomysially, via the perimysium or tendinous attachment. From the periosteal structures and the characteristics of muscular fiber attachments to the bone and periosteum, especially in the ramal and condylar areas, it could be concluded that a mechanical influence of the periosteum on condylar growth is very well possible, which will probably vary during life. The masticatory muscles seemed to be only of minor influence in condylar activity.

Age Factors↗

Effects of periosteum wrapped around tendon in a bone tunnel: A biomechanical and histological study in rabbits.

The present study demonstrated the effects of periosteal autograft on tendon-to-bone healing in the rabbits. In 20 Japanese white rabbits, proximal end of the long digital extensor tendon that was wrapped around by a periosteum was transplanted into a drill hole in the proximal tibial metaphysis. A fresh periosteum was used in the left tibia and a frozen periosteum was used in the right tibia. Six specimens were harvested at each 2, 4, and 6 weeks postoperatively. Radiological features showed progressive remodeling of trabecular bone surrounding the implanted tendon. This remodeling in fresh periosteal graft was earlier than that in frozen graft. Generally, the pull-out strength of the transplanted tendons with a fresh or frozen periosteum increased progressively according to the length of the healing periods. The strength was significantly greater in a fresh periosteal graft than that in a frozen graft at 4 weeks postoperatively. In histological analysis, a 4-week specimen with the fresh periosteal graft showed fibrocartilage formation in the bone tendon interface, whereas the specimens with the frozen graft demonstrated simple approximation of oriented fibrous tissue. In conclusion, the fresh periosteal autograft produced the premature form of fibrocartilagenous attachment in a bone tunnel and provided good mechanical strength.

Animals↗

Regulation of proliferation and osteochondrogenic differentiation of periosteum-derived cells by transforming growth factor-beta and basic fibroblast growth factor.

We studied the effects of transforming growth factor-beta and basic fibroblast growth factor on the regulation of proliferation and osteochondrogenic differentiation of periosteum-derived cells, which have the potential to differentiate into bone and hypertrophic cartilage in vitro. Histological observation revealed that transforming growth factor-beta stimulated chondrogenesis of periosteum-derived cells while basic fibroblast growth factor stimulated proliferation of fibroblast-like cells and inhibited osteochondrogenic differentiation. Immunohistochemical studies revealed that basic fibroblast growth factor inhibited the expression of osteocalcin. Transforming growth factor-beta enhanced uronic acid content but decreased DNA content, alkaline phosphatase activity, and calcium content. In contrast, basic fibroblast growth factor enhanced DNA content but decreased alkaline phosphatase activity, calcium content, and uronic acid content. In addition, transforming growth factor-beta shortened the time-course of gene expression of type-X collagen whereas basic fibroblast growth factor inhibited the gene expression. These results indicate that transforming growth factor-beta stimulates osteochondrogenic differentiation of periosteum-derived cells but inhibits proliferation. They also indicate that basic fibroblast growth factor stimulates proliferation of periosteum-derived cells but inhibits osteochondrogenic differentiation.

Alkaline Phosphatase↗

Experimental craniosynostosis in growing rabbits. The role of the periosteum.

Reports on the role of the periosteum in premature sutural synostosis have been contradictory. The present study summarizes a series of six experiments designed to clarify these previously conflicting findings. Twenty-five male New Zealand White rabbits were divided into six experimental groups. In four of the groups, methyl-2-cyanoacrylate was used to glue the frontal and parietal bones together and temporarily immobilize the coronal suture. In the other two groups, the sutures were not immobilized. Polyethylene was used to separate the cyanoacrylate from the periosteum in two of the groups. The experiments were performed at 5 weeks of age, and the animals were killed at either 30, 45, or 180 days postoperatively. Metallic implants were placed in the frontal and parietal bones for monitoring growth and/or sutural immobilization. Sutural fusion was confirmed radiographically or histologically. Based upon the findings it seems that mechanical immobilization of a suture does not induce fusion of that suture in rabbits. Furthermore, it appears that the mere application of methyl-2-cyanoacrylate to the periosteum overlying a suture will consistently cause the formation of a bony bridge in growing rabbits but not in nongrowing animals. The adhesive does not consistently induce synostosis if the periosteum is excised.

Animals↗

Gene marking in adeno-associated virus vector infected periosteum derived cells for cartilage repair.

OBJECTIVE: To evaluate both the potential for transferring genes to periosteal cells using an adeno-associated virus (AAV) vector and the potential for gene expression after transplantation of those cells to a cartilage defect in vivo. METHODS: Periosteum was obtained from the tibia of 6-week-old rabbits and enzymatically digested. The isolated periosteum derived cells were cultured and the subconfluence cells were infected with a recombinant AAV expressing the LacZ gene (AAV-LacZ). Collagen gel containing the LacZ transferred, periosteum derived cells was transplanted into a full thickness articular cartilage defect in 10 rabbits. RESULTS: Infected cells still growing on the plate continued to express LacZ at least 12 weeks after AAV infection, with the highest percentage of LacZ positive cells reaching 74.4%. The LacZ positive cells were recognized at the transplant sites in 8 out of 10 knees. CONCLUSION: Gene expression in periosteum derived cells was sustained in vitro for at least 12 weeks using the AAV vector, and for 2 weeks ex vivo after transplantation into a cartilage defect.

Adenoviruses, Human↗

[Comparison of biomechanical properties between human nasal periosteum and fascia].

There has been a lot of controversies on which layer the silastic implants should be inserted in the augmentation rhinoplasty, i.e. subperiosteal or deep subfascial. This study is to investigate the biomechanical properties of human nasal periosteum and deep fascia, including tensile strength, stress-strain and stress relaxation characters under uniaxial tension system. The periosteum is stronger in tensile strength than that of the fascia, but it is less elastic. Under a sudden increase of load, the periosteum relaxes far less than the fasia. Therefore, in view of biomechanics, the periosteum is thicker, tougher, stiffer and less relaxation than facia, thus has a better fixation effect.

Biomechanical Phenomena↗

[An experimental study on the repair of the necrotic tubular bone with pedicled vascular periosteum grafting in rabbits].

OBJECTIVE: To investigate the mechanism of the repair of the necrotic tubular bone with pedicled vascular periosteum grafting in rabbits. METHODS: Twenty mature New Zealand rabbits aged 8 months were randomly divided into test and control groups by placebo-controlled protocol. A segment of radius measuring 1.2 cm in length with pedicled vascular periosteum of the rabbits in the test group was obtained from the middle distal part of the bone, and boiled for 30 minutes. The cooled bone was then re-grafted and wrapped with vascularized periosteum and immobilized, while those in the control group, no periosteal grafting was done. X-ray examinations of the bones were carried out at 2, 4, 6, 8 approximately 10 post operation weeks (POWs). Meanwhile 4-5 rabbits were sacrificed for the harvesting of the radius on both sides for histological examination. RESULTS: It was revealed by X-ray and histological study that the periosteal hyperplasia could be observed 2-4 weeks after operation in the test group. The sign of union of the fracture and the formation and reconstitution of the trabeculae could be observed 6-8 weeks after operation. The reconstitution of reticulated bone, the formation of the lamellar bone and new haversian system could be observed during 8-10 POW. The structure of the new formed bones became more mature and the fracture healed at 12 POW. In contrast, there was no changes in the necrotic bones in the control group at 2 POW and no signs of fracture healing at 4-6 POW, and the defect of the bones could be observed at 8 POW. The necrotic bones were totally dissolved and absorbed, and the bone defects could be observed clearly filled with fibrotic tissues at 12 POW. CONCLUSION: The necrotic bones could be replaced by regeneration of new bone originated from the pedicled vascular periosteum, so that the necrotic tubular bones could be repaired. But the necrotic bones in the control group were eventually absorbed, resulting in bone defects.

Animals↗

[Long-term clinical observation on the repair of large articular cartilage defects of the hip and the knee with free autogeneous periosteum].

OBJECTIVE: To observe the long-term clinical results of repairing large articular cartilage defects of the hip and the knee with free autogeneous periosteum. METHODS: Based on the results of experimental studies, the authors used free autogeneous periosteum transplantation and postoperative continuous passive motion (CPM) to repair large articular cartilaginous defects in 52 patients from February 1987 to August 1995. Of 37 patients with complete follow-up data, 16 had congenital dislocation of the hip, 6 traumatic arthritis of hip, 1 femoral head destruction following mild infection, 2 ankylosing spondylitis, 6 intra-articular fracture of the knee, 4 arthritis of the knee and 2 stiff knee following joint infection. The patients with dislocation of hip were given relieving traction before operation. The cartilages of pathological changes were excised to bleeding bone. The defects were repaired with periosteum removing from tibia. CPM were immediately applied for 4-6 weeks and no bearing was allowed 6 months after discharge. The silicon membrane was taken out in the 6th month. RESULTS: Thirty-seven patients (17 males, 20 females) were followed up 7-15 years with an average of 10.5 years. The functional evaluation referred to joint pain degree, joint mobile range, daily activity and X ray findings. The results were excellence in 11 patients, good in 18 patients, poor in 8 patients. CONCLUSION: The method to repair articular cartilage defect with free autogeneous periosteum is effective and may be applied clinically.

Adolescent↗

[A comparison study on autologous periosteum-wrapped tendon and spongiosa homogenate as a substitute for lunate].

OBJECTIVE: To study and compare bone-forming mechanism after compound of autologous periosteum-wrapped tendon with spongiosa homogenate and other implants in articular cavity, and to explore the possibility of the compound as a substitute for the lunate in Kienbock's disease. METHODS: Forty-five New Zealand white rabbits were randomly divided into three groups: periosteum group (group A, n=15), composite group (group B, n=15), and control group (group C, n=15). The three sorts of implants were placed into articular cavity of the knee respectively. The changes of bone formation and bone morphogenetic protein (BMP) distribution of the implants were examined under optical microscope with HE and immunohistochemical staining and measured by CT 3, 6 and 9 weeks after operation. RESULTS: The result of BMP staining was negative after 3 weeks and positive in new cartilage cells after 9 weeks in group A. The positive BMP staining was observed in group B after 3 weeks and 9 weeks, which mainly distributed in new bone cells and cartilage cells. And negative BMP staining was observed every stage in group C. The quantitative CT bone mineral density (BMD) values of 3 implants were analyzed, the difference was significant between the groups (P<0.01), except that between groups A and C in the 3rd week (P>0.05). CONCLUSION: The above results demonstrated that the compound of autologous periosteum-wrapped tendon and spongiosa homogenate can produce bone and cartilage massively under the induction of periosteum and bone-forming factors such as BMP in spongiosa homogenate and the compound can be used as a substitute for the lunate.

Animals↗

[Effects of periosteum, synovium and cartilage tissues on genes for joint cartilage regeneration].

OBJECTIVE: To study the effects of the periosteum,synovium and cartilage tissues on the gene expressions of proteoglycan, collagen II, and nuclear factor kappa B (NF-kappaB) and to investigate the different effects of these tissues on cartilage regeneration. METHODS: In 20 New Zealand white rabbits, 20 cartilage explants were taken from the knee joints in each rabbit, the size of which was 4 mm x 4 mm x 4 mm. All the cartilages were divided into the following 4 groups and cultured for 7 days: Group A, with 5 pieces (2 mm x 2 mm) of the synovium of the knee joints in each dish; Group B, with 5 pieces (2 mm x 2 mm) of the periosteum in each dish; Group C, with 5 pieces (2 mm x 2 mm x 2 mm) of the cartilage in each dish; and Group D, with no addition of other tissues (control group). RNA was extracted from the cells of the cartilage explants (4 mm x 4 mm x 4 mm) in all the dishes. The gene expressions of proteoglycan, collagen II and NF-kappaB were defected by a reverse transcription-polymerase chain reaction (RT-PCR). RESULTS: In group A, the gene expression of proteoglycan was significantly decreased. The relative density of this gene expression had a significant difference when compared with that in group D (1.09 +/- 0.21 vs. 1.25 +/- 0.25, P < 0.05); the gene expressions of collagen I and NF-kappaB were also decreased, but they had no significant differences when compared with those in group D (P > 0.05). In group B, the gene expressions of proteoglycan, collagen II, and NF-kappaB were significantly increased. The relative densities of these gene expressions were 1.60 +/- 0.26, 1.57 +/- 0.24, and 4.20 +/- 2.22, respectively, which had significant differences when compared with those in group D (P < 0.05). In group C, the relative density of the gene expression of collagen II was 1.43 +/- 0.28, which had a significant difference when compared with that in group D (P < 0.05), but the relative densities of the gene expressions of proteoglycan and NF-kappaB had no significant differences when compared with those in group D (P > 0.05). CONCLUSION: The results indicate that the periosteum can up-regulate the gene expressions of proteoglycan, collagen II and NF-kappaB. The NF-kappaB is likely to be an important nuclear transcription factor related to cartilage regeneration. The results also suggest that the periosteum may be better in facilitating the cartilage repair and regeneration in clinical practice.

Animals↗

[Features of the femur periosteum and endosteum structure in rodents and hares].

General and some special histologic methods have been used to study the structure of periosteum and endosteum, as well as the morphological peculiarities of their cells in rodents and hares in the early and late postnatal ontogenesis. It is established that the periosteum of animals under study is represented by a two-layer structure: the outer (protective) layer and the inner (osteogenic) one. The outer layer consists of fibroblast-like cells, the inner one of osteogenic cells (pre-osteoblasts and osteoblasts). Endosteum is represented only by osteogenic cells and, unlike the periosteum, possesses no independent fibrillar structure; therefore, it appears to be more labile than the periosteum.

Animals↗

Ultrastructure of the periosteum from membrane bone.

Specimens of skull and palate were taken from 7 beagle dogs after perfusion and the periosteum examined by light and electron microscopy. Three zones were evident in the periosteum, differing in terms of the proportion of cells, fibres and matrix. Zone I consisted of osteoblasts adjacent to the bone surface and a supraosteoblast layer of smaller, compact cells, Zone II was a relatively translucent zone with numerous capillaries and Zone III consisted of cells intermingled with collagen fibrils. Quantification of the relative volumes of tissue components using stereology indicated significant differences between the three zones in each bony site, but not between the two sites. Measurement of numerical density, surface density, profile cross-sectional area, cell volume and cell surface/volume ratio of fibroblast-like cells revealed marked differences between these cells in Zone I and the other two zones; it is possible that the fibroblast-like cells seen in Zone I represent osteoprogenitor cells. Zone II represents the classical cambial layer and contains the majority of the vascular elements present in the periosteum. Zone III contains large volumes of fibroblasts and collagen fibrils and corresponds to the classical fibrous layer. The similarity of this zonal organisation in different regions suggests that periosteum has a consistent structure in membrane bone.

Animals↗

Bone morphogenetic protein-mediated interaction of periosteum and diaphysis. Citric acid and other factors influencing the generation of parosteal bone.

In rabbits, after long-bone growth is complete and the cambium layer regresses, mesenchymal-type cells with embryonic potential (competence) for bone development persist in the adventitial layer of periosteum. These cells are not determined osteoprogenitor cells (stem cells) because bone tissue differentiation does not occur when adult periosteum is transplanted into a heterotopic site. In this respect, adventitial cells differ from bone marrow stroma cells. In a parosteal orthotopic site in the space between the adult periosteum and diaphysis, implants of bone morphogenetic protein (BMP) and associated noncollagenous proteins (BMP/NCP) induce adventitia and adjacent muscle connective-tissue-derived cells to switch from a fibrogenetic to a chondroosteoprogenetic pattern of bone development. The quantity of induced bone is proportional to the dose of BMP/NCP in the range from 10 to 50 mg; immature rabbits produced larger deposits than mature rabbits in response to BMP/NCP. Preoperative local intramuscular injections of citric, edetic, or hyaluronic acids in specified concentrations markedly enhanced subperiosteal BMP/NCP-induced bone formation. The quantity of bovine or human BMP/NCP-induced bone formation in rabbits is also increased by very low-dose immunosuppression but not by bone mineral, tricalcium phosphate ceramic, inorganic calcium salts, or various space-occupying, unspecific chemical irritants. Although composities of BMP/NCP and allogeneic rabbit tendon collagen increased the quantity of bone in a parosteal site, in a heterotopic site the composite failed to induce bone formation. In a parosteal site, the conditions permitting BMP/NCP-induced bone formation develop, and the end product of the morphogenetic response is a duplicate diaphysis. How BMP reactivates the morphogenetic process in postfetal mesenchymal-type adventitial cells persisting in adult periosteum (including adjacent muscle attachments) is not known.

Animals↗

Normal and heterotopic periosteum.

Normal periosteum is an osteoprogenitor cell-containing bone envelope, which can be activated to proliferate by trauma, retroviruses, tumors, and lymphocyte mitogens. Activated periosteum produces cartilage and bone, and is colonized by bone-resorbing cells. The osteogenic activity of periosteum is maintained in heterotopic sites and in vitro. Ectopic bone, however, is colonized by bone marrow precursor cells but does not develop a true periosteum. The absence of true periosteal envelope in the heterotopically induced bone may be the major, if not the only, difference between heterotopic and orthotopic bone deposits.

Animals↗

Growth of transplants of rat humerus following circumferential division of the periosteum.

The growth of transplants of young rat humeri has been studied following circumferential division of the periosteum at either the proximal or the distal end of the shaft. Periosteal division resulted in bones that were longer than those in which the periosteum was not cut. Following proximal division the experimental bones grew 30% more at both ends than the control bones and 16% more at the proximal end following distal division. There was, however, no difference between the growth of the experimental and control bones at the distal end following distal division of the periosteum. The experimental humeri had less new subperiosteal bone deposited over their diaphyses than the control humeri. These findings support the view that the periosteum is under tension as a result of the activity of the growth plates, and that changes in periosteal tension affect both the growth in length and the deposition of subperiosteal bone.

Animals↗

The blood supply of the periosteum.

Twelve goat limbs were injected with red latex and then carefully dissected to display the vessels of the periosteum. The blood supply of periosteum was found to be derived from four sets of vessels: (1) Intrinsic periosteal system. (2) Musculoperiosteal system. (3) Fascioperiosteal system. (4) Cortical capillary anastomoses. The intrinsic system of vessels lay within the fibrous layer of the periosteum. According to the pattern of these vessels they could be divided into: (a) a short vessel pattern, where there were many small vessels with no predominant direction; (b) a circular pattern, where the vessels encircled the bone; (c) a longitudinal pattern, where the vessels ran parallel to the long axis of the bone. The musculoperiosteal system consisted of connections between the muscle circulation and the periosteal vessels at the sites of muscle origin. The fascioperiosteal system consisted of branches from a limb artery that ran in a fascial plane between muscles to supply the periosteum. The cortical capillary anastomosis consisted of capillaries that ran in the bone cortex between the intramedullary circulation and the periosteal vessels.

Animals↗