1.Distribution and property of nerve fibers in human long bone tissue.
Bin CHEN ; Guo-xian PEI ; Dan JIN ; Kuan-hai WEI ; Yu QIN ; Qing-si LIU
Chinese Journal of Traumatology 2007;10(1):3-9
OBJECTIVETo observe the distribution of the nerve fibers in the bone tissue and the entry points of these fibers into the bone.
METHODSThe adult tibia was used for the ground sections which were afterwards made into the slice sections by decalcification in ethylenediamine tetraacetic acid (EDTA). The ground sections were stained in silver and the slice sections were stained in silver and haematoxylin and eosin (HE) respectively. Then, the samples of the transmission electron microscope and the atomic force microscope were made and observed.
RESULTSIn the human long bone tissue, many nerve fibers were distributed in the membrane, cortical bone, cancellous bone and marrow. The nerve fibers entered the bone from the nutrient foramen, and passed through the nutrient canal, Haversian's canal and Volkmann's canal, and finally into the bone marrow. In the nutrient canal, the nerve fibers, mainly the medullary nerve fibers, followed the blood vessel into the bone. In the cortical bone, the nerve fibers also followed the blood vessels and were mainly distributed along Haversian's canal and Volkmann's canal. In the bone trabecular and bone marrow, there were many nerve fiber endings arranged around the blood vessels, mainly around the tunica media of medium-size arteries in the marrow and around capillary blood vessels, and a few scattered in the bone marrow. There were sporadic nerve endings in epiphyseal plate and no nerve fibers permeated epiphysis to diaphysis. No distribution of nerve fibers could be found in cartilaginous part.
CONCLUSIONSThere are many nerve fibers in bone and the nerve passageway is nutrient foramen, Volkman's canal, Haversian's canal and bone marrow.
Adult ; Humans ; Microscopy, Atomic Force ; Microscopy, Confocal ; Microscopy, Electron, Scanning ; Nerve Fibers ; ultrastructure ; Staining and Labeling ; Tibia ; anatomy & histology ; innervation ; ultrastructure
2.Comparation on Haversian system between human and animal bones by imaging analysis.
Hui-Ling LU ; Jing ZHENG ; Ya-Nan YAO ; Sen CHEN ; Hui-Pin WANG ; Li-Xian CHEN ; Jing-Yuan GUO
Journal of Forensic Medicine 2006;22(2):97-100
OBJECTIVE:
To explore the differences in Haversian system between human and animal bones through imaging analysis and morphology description.
METHODS:
Thirty-five slices grinding from human being as well as dog, pig, cow and sheep bones were observed to compare their structure, then were analysed with the researchful microscope.
RESULTS:
Plexiform bone or oeston band was not found in human bones; There were significant differences in the shape, size, location, density of Haversian system, between human and animal bones. The amount of Haversian lamella and diameter of central canal in human were the biggest; Significant differences in the central canal diameter and total area percentage between human and animal bones were shown by imaging analysis.
CONCLUSION
(1) Plexiform bone and osteon band could be the exclusive index in human bone; (2) There were significant differences in the structure of Haversian system between human and animal bones; (3) The percentage of central canals total area was valuable in species identification through imaging analysis.
Adult
;
Animals
;
Bone and Bones/ultrastructure*
;
Cattle
;
Dogs
;
Haversian System/ultrastructure*
;
Humans
;
Image Processing, Computer-Assisted
;
Microscopy, Electron
;
Sheep
;
Species Specificity
;
Swine
;
Tibia/ultrastructure*
3.Analysis of apposition on differently treated implant surface at early stage of implantation.
Fu-ming HE ; Song CHEN ; Shan-shan ZHAO
Journal of Zhejiang University. Medical sciences 2006;35(5):472-478
OBJECTIVETo compare the surface apposition and the bone response at early period of implantation in two differently treated implants.
METHODSThe implants were subject to double acid-etched-H2O2/HCl-heat treatment and double acid-etching treatment, and then randomly implanted into the tibia of rabbits. After 2, 4, 8 weeks of follow up, the bone specimens containing implants were prepared and examined by a field emission SEM and EDX.
RESULTA layer rich with calcium and phosphorus was clearly demonstrated on the implants surface of both groups after 2 weeks of implantation, but it was mostly disappeared after 4 weeks. There were large amounts of osteoblasts cells on double acid-etched-H2O2/HCl-heat treated implants surface indicating the initiation of osteogenesis. After 8 weeks of implantation some new bones were attached on the implants surface in both groups, more bones attached were shown on double acid-etched- H2O2/HCl-heat treated implants surface.
CONCLUSIONA calcium and phosphorus-rich layer was formed on the implants surface of both groups at early period of implantation.
Animals ; Dental Implantation ; Dental Implants ; Dental Materials ; chemistry ; Dental Prosthesis Design ; Hydrogen Peroxide ; chemistry ; Osseointegration ; physiology ; Osteogenesis ; physiology ; Rabbits ; Surface Properties ; Tibia ; surgery ; ultrastructure ; Titanium ; chemistry