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Biomedical subjects

C B Johansson

Publications and source records attributed to C B Johansson.

At least 37 records · Page 2Linked to original sources

No biological advantage with a low temperature curing versus a conventional bone cement: an experimental, mechanical and histomorphometrical study in the rabbit tibia.

Both tibial marrow cavities of 12 rabbits were evacuated and filled with curing bone cement. In one of the tibias conventional curing bone cement (Simplex P) was injected, while the other tibia of the same animal was filled with a low temperature curing bone cement (Boneloc). Three titanium implants were inserted along the proximal metaphysis of each tibia. Eight weeks after insertion the most distal implant in each tibia was removed while recording the removal torque. The implant was then once again screwed home into its bone bed. The animals were sacrificed 16 weeks after implant insertion. The previously removed implant and another implant in each tibia were then both removed while recording the removal torque. The third implant in each tibia was cut out en bloc with surrounding tissue and processed for ground section. We found no statistical differences in the mechanical or the histomorphometric evaluation of implant integration between the two cements, indicating that the low temperature curing bone cement does not result in a significantly different bone response from that of a conventional acrylic cement.

Journal Article↗

Bone-tissue formation and integration of titanium implants: an evaluation with newly developed enzyme and immunohistochemical techniques.

BACKGROUND: Examination of the tissue surrounding retrieved implants involve routine investigations on cut and ground sections. Undecalcified sections with implants in situ are histologically stained followed by qualitative and quantitative observations of the tissue response to the implants by light microscopy. PURPOSE: A novel technique that allows for the accurate definition and quantification of enzymes involved in bone formation (alkaline phosphatase) and resorption (acid phosphatase) in the tissue is presented. MATERIALS AND METHODS: Commercially pure titanium and titanium alloy (Ti6Al4V) implants were retrieved after 6 and 12 weeks of healing in rabbit bone. In addition, 4-week specimens from commercially pure titanium bone harvest chambers placed in rabbit bone were used. Undecalcified cut and ground sections were produced and evaluated with enzyme and immunohistochemical staining techniques. RESULTS: The titanium implants retrieved after 6 weeks of insertion in rabbit bone revealed a higher activity of both alkaline phosphatase and acid phosphatase activity compared to the implants followed for 12 months. The former samples revealed ongoing bone-tissue remodeling in the interface, whereas the latter ones showed steady-state bone conditions. Applying the new technique allowed for investigation of various bone proteins present in the tissue that had formed inside titanium canals of harvest chambers at various times of follow-up. CONCLUSIONS: The combination of routine histologic stainings with enzyme and immunohistochemical technique of cut and ground specimens is a valuable tool in the investigations of retrieved implants from humans and animals. This novel technique now may be used to describe the state of bone regeneration in the interface zone associated with implant research.

Acid Phosphatase↗

Retinoid-X receptor signalling in the developing spinal cord.

Retinoids regulate gene expression through the action of retinoic acid receptors (RARs) and retinoid-X receptors (RXRs), which both belong to the family of nuclear hormone receptors. Retinoids are of fundamental importance during development, but it has been difficult to assess the distribution of ligand-activated receptors in vivo. This is particularly the case for RXR, which is a critical unliganded auxiliary protein for several nuclear receptors, including RAR, but its ligand-activated role in vivo remains uncertain. Here we describe an assay in transgenic mice, based on the expression of an effector fusion protein linking the ligand-binding domain of either RXR or RAR to the yeast Gal4 DNA-binding domain, and the in situ detection of ligand-activated effector proteins by using an inducible transgenic lacZ reporter gene. We detect receptor activation in the spinal cord in a pattern that indicates that the receptor functions in the maturation of limb-innervating motor neurons. Our results reveal a specific activation pattern of Gal4-RXR which indicates that RXR is a critical bona fide receptor in the developing spinal cord.

Animals↗

Nerve growth factor induces process formation in meningeal cells: implications for scar formation in the injured CNS.

Nerve growth factor (NGF) induces the differentiation and supports the survival of subpopulations of neurons in the PNS and CNS. Here we report that meningeal cells in the pia mater express immunoreactivity and mRNA for both known NGF receptors, the low-affinity receptor p75 and the tyrosine kinase receptor trkA. NGF induces rapid tyrosine phosphorylation of trkA in meningeal cells in vitro. NGF does not stimulate proliferation of primary meningeal cells but induces process outgrowth. p75- and trkA-immunoreactive meningeal cells with long processes, resembling NGF-treated cells in vitro, are abundant in the scar tissue that forms at spinal cord lesions in rat and cat. These data suggest that NGF, which is expressed at increased levels in the brain and spinal cord after lesions, may be involved in scar formation in the injured CNS.

Animals↗

Central nervous system stem cells in the embryo and adult.

The central nervous system is generated from neural stem cells during embryonic development. These cells are multipotent and generate neurons, astrocytes and oligodendrocytes. The last few years it has been found that there are populations of stem cells also in the adult mammalian brain and spinal cord. In this paper, we review the recent development in the field of embryonic and adult neural stem cells.

Adult↗

The effect of hyperbaric oxygen treatment on bone tissue reactions to c.p. titanium implants placed in free autogenous bone grafts. A histomorphometric study in the rabbit mandible.

This study aimed to investigate the effect of hyperbaric oxygen (HBO) therapy on the tissue reactions to commercially pure (c.p.) titanium implants placed in free autogenous bone graft by a 1-stage procedure. Eighty c.p. titanium implants were placed in the bone grafted from iliac crest to bilateral mandible of 40 Japanese white rabbits without tapping. Twenty rabbits underwent daily a HBO treatment for 60 min under 2.4 ATA during 20 consecutive days and the other untreated 20 rabbits served as controls. The implants with surrounding bone tissue were retrieved 20, 30, 60, 90 and 120 days after surgery, fixated, dehydrated and embedded in resin. About 20 microns thick ground sections were prepared prior to microscopical observations. The bone area and the bone-to-implant contact inside the threads were calculated separately in the grafted bone and in the host bone for each implant. After 30 and up to 120 days, the HBO treated group showed more bone-to-implant contacts in the grafted bone as compared to the non-HBO treated group. In the host bone there were no differences observed between HBO and non-HBO treated groups. This study indicated that HBO treatment was beneficial for the tissue incorporation of c.p. titanium implants when placed immediately in free autogenous bone grafts.

Animals↗

Quantitative and qualitative investigations of surface enlarged titanium and titanium alloy implants.

Screw shaped implants of commercially pure (c.p.) titanium and titanium-6aluminum-4vanadium (Ti6A14V) were blasted with particles of TiO2 of mean sizes of 25 microns (Group I) and 75 microns (Group II) and inserted in rabbit bone for 3 months. The surface roughness of the implants was examined and quantified with an optical scanning 3-dimensional instrument (TopScan 3D system), revealing the two alloy surfaces in each group had similar surface roughness. Biomechanical (removal torque) tests showed the c.p. titanium implants to be significantly more stable in the bone bed than those of Ti6A14V. In Group I, the c.p. titanium implants demonstrated a mean removal torque of 38 N cm while the Ti6A14V demonstrated a mean removal torque of 27 N cm (P = 0.004). Group II implants revealed a mean removal torque of 70 N cm for the c.p. ti and 50 N cm for the alloy samples (P = 0.003). The removal torque values were converted to shear forces/strengths by three calculation methods, based on (a) the entire length of the implant surface in the cortical region, (b) the thickness of the cortical bone measured in close vicinity to the thread peaks and (c) the bone-metal contact length measured on the non-unscrewed neighbouring implants. Group I: (a) the c.p. ti implants revealed a mean shear force of 4 vs a mean of 3 N/mm2 for the alloy samples. Shear strengths based on (b); were 8 for c.p. ti vs 6 N/mm2 for the alloy. The mean shear strength/force if calculated according to (c) revealed 23 for c.p. ti vs 18 N/mm2 for the alloy. Corresponding numbers for Group II; (a) c.p. ti 8 compared to 6 N/mm2 for the alloy, (b) c.p. ti demonstrated a mean value of 17 vs 11 N/mm2 for the alloy. According to method (c); c.p. ti had a mean shear strength of 26 vs 22 N/mm2 for the alloy samples. Histomorphometrical comparisons were performed on 10 microns thick undecalcified ground sections in the light microscope. In both Group I and Group II, the calculations of the mean bone-to-metal contact demonstrated more bone in contact to the c.p. titanium implants than to the Ti6A14V ones. Whereas comparisons of the bone volume inside the threads demonstrated slightly higher bone volumes around the alloy samples, no statistically significant difference was obtained between the two materials histomorphometrically.

Alloys↗

Removal of titanium implants from the temporal bone: histologic findings.

OBJECTIVE: This study aimed to evaluate the histologic examination of bone tissue surrounding three titanium implants, which were removed since the patients presented with long-standing pain in the implant area. The histologic examination was both qualitatively and quantitatively performed. Furthermore, could an explanation be obtained for the pain in the implant area, which, after removal of the percutaneous implant, disappeared immediately? STUDY DESIGN: Retrospective case review; clinical histomorphometric. SETTING: University Hospital Nijmegen, Göteborg University, Sweden. PATIENTS: Three patients of a consecutive series of 189; 1 man and 2 women who had received a bone-anchored, percutaneous, skin-penetrating, commercially pure titanium implant in the temporal bone, on which a transducer was mounted. The implants were removed because of pain in the implant area from the three patients after 31 months, 18 months, and 8 months, respectively. MAIN OUTCOME MEASURES: The percentage of direct bone-to-metal contact was 81%, 59%, and 42%, respectively. The percentage of bone volume between the threads of the screw was 90, 78, and 75, respectively. RESULTS: The qualitatively histologic findings showed no major differences among the three investigated samples. Quantitatively, the amount of osseointegration depended on the duration of implantation. CONCLUSIONS: Direct bone-to-metal contact and the bone volume between the threads increased as the implantation time increased. No explanation was found for the longstanding pain in the implant area and the relief of pain after removal of the percutaneous implant.

Adult↗

Bone tissue reactions to an electrophoretically applied calcium phosphate coating.

Oral implants of a threaded design, calcium phosphate (CaP)-coated using an electrophoretic deposition technique, were compared to uncoated commercially pure (c.p.) titanium control in an animal study with 4 weeks and 6 months of follow-up, respectively. The 3D surface roughness of a CaP-coated implant was about three times greater than that of an uncoated control. Histomorphometric analyses of the direct bone-implant contact demonstrated a short-term advantage to the CaP-coated implants, whereas no significant difference to the uncoated titanium was found after 6 months. Comparison of the amount of bone inside or outside the threads showed similar values for test and control after 4 weeks. Significantly higher amounts of bone outside the uncoated c.p. titanium implants were measured after the long-term follow-up.

Animals↗

Norditerpenoids and diterpenoids from Salvia multicaulis with antituberculous activity.

From the roots of Salvia multicaulis, four new aromatic norditerpenoids, multicaulin (1), 12-demethylmulticauline (2), multiorthoquinone (3), and 12-demetylmultiorthoquinone (4), two new abietane diterpenoids, 12-methyl-5-dethydrohorminone (5) and 12-methyl-5-dehydroacetylhorminone (6), as well as a new pimarane diterpenoid, salvipimarone (7), were isolated. Also obtained in this investigation were the known compounds alpha-amyrin, hinokione, horminone, lupeol, manool, 1-oxoferruginol, 18-oxoferruginol, pisiferal, and sempervirol. The structures of compounds 1-7 were established by 1D and 2D NMR techniques and by chemical methods. The antituberculous activity of 1-7 was tested against Mycobacterium tuberculosis strain H37Rv, and all compounds were found to be significantly active, with 2 and 4-6 being the most potent substances. Six of these novel compounds were evaluated against a number of additional bacterial cultures.

Antitubercular Agents↗

Short- and long-term animal studies with a plasma-sprayed calcium phosphate-coated implant.

A commercially available hydroxyapatite (HA)-coating was investigated in a 4- and 24-week animal study. HA-coated and uncoated commercially pure (c.p.) titanium threaded implants were inserted in rabbit tibia and femur. Qualitative histology showed giant cells and macrophages around both types of implants. Histomorphometry demonstrated significantly more bone in contact to the HA-coated specimens at both follow-up periods. In contrast, bone area measurements (the amount of bone inside and/or outside the threads) revealed significantly higher percentages of bone around the uncoated c.p. titanium controls after 6 months of follow-up. The inferior amount of bone around the HA-coated implants in the longer-term perspective may relate to macrophage-induced resorption.

Animals↗

Improved long-term bone-implant integration. Experiments in transgenic mice overexpressing bovine growth hormone.

Several recent studies have investigated the effects of growth hormone (GH) on the healing of fractures and bone ingrowth, but with conflicting results. The negative results may be due to antibody formation against injected GH or because some experimental models are able to prove only positive GH effects. In this study, we wanted to investigate the effect of GH on implant integration in bone. To avoid potential formation of antibodies against injected GH, we used a model with transgenic mice overexpressing bovine GH (bGH). Titanium implants were inserted in the forehead of the mice. 4 months after insertion, the implants were cut out en bloc with the surrounding bone. The calcified specimens were cut and ground to a thickness of approximately 10 microns. Histomorphometry demonstrated significantly more direct bone-to-metal contact in the transgenic mice than in the nontransgenic littermates. Our findings indicate that systemic administration of GH in humans may improve implant integration in bone.

Animals↗

Titanium-anchored prostheses in otology.

In the late 1970s, Per-Ingvar Branemark and coworkers in Goteberg, Sweden, successfully introduced osseointegrated titanium implants into clinical practice. They had achieved the previously elusive goal of producing stable, secure percutaneous implants anchored in underlying cortical bone. Two applications of these implants to otology were obvious: (1) to provide a coupling for bone-conduction hearing aids and (2) to provide fixation points for anchoring of auricular prostheses. Before describing the current state of these clinical applications and considering future potential uses, the authors review the basis for titanium osseointegration.

Bone Conduction↗

Cutting directions of bone with biomaterials in situ does influence the outcome of histomorphometrical quantifications.

Ten commercially pure titanium implants were inserted in the tibia of ten mature New Zealand white rabbits for a healing period of 3 months. Cut and ground sections were performed on transversely and longitudinally cut tibia bone with implants in situ. Each implant with surrounding bone was processed by (a) dividing it into two parts by cutting transversely through the tibia and then (b) cutting one of the implant halves longitudinally through the tibia. In both cases 10 microns sections were made. Computerized histomorphometrical calculations of the bone-to-metal contact and the bone area in the threads were performed and comparisons of the differently cut sections were made for the same implant. Larger amounts of bone-to-metal contact and bone area in the threads were observed in the longitudinally cut samples in comparison to transversely cut ones. A strong statistically significant difference was obtained when comparing the transversely with the longitudinally cut samples with respect to bony contacts in the cortical region, demonstrating 25% more bone-to-metal contact lengths in the longitudinal cutting direction of the tibia. Quantitative histomorphometrical comparisons should, therefore, be performed on samples that are cut in the same direction.

Animals↗

Importance of ground section thickness for reliable histomorphometrical results.

Ten screw-shaped commercially pure titanium implants were inserted in 10 rabbit tibia. The implants with surrounding bone were harvested after 12 weeks. The samples were processed to be cut and ground. Histomorphometrical analyses of the bone-to-metal contact and the bone area around the entire implants were performed on transvertically cut sections at intervals, starting with 100 microns thick sections; then the same sections were further ground down to 50, 30 and 10 microns. The thicker the section the more bone-to-metal contacts were demonstrated. A statistically significant difference was obtained when comparing the 100-30, 100-10, 50-30 and the 50-10 microns thick sections. Comparing the area measurements of 100-10, 50-30, 50-10 and 30-10 microns revealed a statistically significant difference. Bone-to-metal contact measurements on ground sections that are too thick (over 30 microns) may result in overestimations of the 'true' bony contacts.

Animals↗

Spinal axons in central nervous system scar tissue are closely related to laminin-immunoreactive astrocytes.

Although transected central nervous system axons fail to regrow after injuries in adult mammals, they send sprouts into the scar tissue that forms at the lesion. We have investigated the relation between scar cells, laminin-like immunoreactivity and cut spinal axons in two previously characterized spinal cord lesion types. Labeling with antisera to glial fibrillary acidic protein and laminin demonstrated that the scar tissue formed after lesions in the rat and cat dorsal and ventral funiculi showed prominent gliosis and strong laminin-like immunoreactivity four days to one year postlesion. Axonal sprouts in the scar, visualized with antibodies to neurofilament (RT97) or by tracing using fluorescein-conjugated dextran, were ensheathed by a thin layer of strongly laminin-immunoreactive tissue. Immunoelectron microscopy demonstrated that axons in the scar were ensheathed predominantly by astrocytes, and that the surface of the cells outlining the axons in the scar showed strong laminin-like immunoreactivity. Adhesive and neurite orienting properties in the scar tissue were assessed in an in vitro system where PC12 cells were cultured on spinal cord slices from dorsal funiculus-lesioned rats. Very few cells adhered to the spinal cord section except for the part where the scar tissue had formed, where numerous cells were attached. The PC12 cells that had adhered to the scar tissue were mainly seen in parts of the scar that showed laminin-like immunoreactivity and their neurites predominantly followed tissue showing laminin-like immunoreactivity. The close association between axonal sprouts and laminin-like immunoreactivity indicates a role for laminin in axonal growth and/or guidance in the injured spinal cord.

Animals↗

Rapid, widespread, and longlasting induction of nestin contributes to the generation of glial scar tissue after CNS injury.

Neuronal regeneration does generally not occur in the central nervous system (CNS) after injury, which has been attributed to the generation of glial scar tissue. In this report we show that the composition of the glial scar after traumatic CNS injury in rat and mouse is more complex than previously assumed: expression of the intermediate filament nestin is induced in reactive astrocytes. Nestin induction occurs within 48 hours in the spinal cord both at the site of lesion and in degenerating tracts and lasts for at least 13 months. Nestin expression is induced with similar kinetics in the crushed optic nerve. In addition to the expression in reactive astrocytes, we also observed nestin induction within 48 hours after injury in cells close to the central canal in the spinal cord, while nestin expressing cells at later timepoints were found progressively further out from the central canal. This dynamic pattern of nestin induction after injury was mimicked by lacZ expressing cells in nestin promoter/lacZ transgenic mice, suggesting that defined nestin regulatory regions mediate the injury response. We discuss the possibility that the spatiotemporal pattern of nestin expression reflects a population of nestin positive cells, which proliferates and migrates from a region close to the central canal to the site of lesion in response to injury.

Animals↗