Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników

Znaleziono wyników: 9

Liczba wyników na stronie
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 1 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników

Wyniki wyszukiwania

help Sortuj według:

help Ogranicz wyniki do:
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 1 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników
The purpose of this experiment was to optimize the methodology of culturing predegenerated Schwann cells. Right sciatic nerves of adult rats (n=3) were cut and left for 7 days. Then, 1-mm fragments of predegenerated (P) and intact (C) nerves were separately planted in 12-well culture plates precoated with laminin or fibronectin. Medium for culturing of endothelial cells EBM-2 (endothelial cell culture medium) was compared with DMEM (Dulbecco’s Modified Eagle’s Medium). Additionally, culture media were supplemented with factors supporting SCs growth: bovine pituitary extract (5 µg/ml), heregulin (40 ng/ml), and insulin (2.5 ng/ml). After 7 or 14 days, plates were subjected to analysis. Cell culture purity was determined under the fluorescent microscope by estimating the percentage of GFAP, N-Cadherin and NGFR p75-positive cells, and intensity of cell growth - by counting the number of cell islets migrating from nerve explants. Percentage of cells confirmed as Schwann cells was 94–97. Number of islets was significantly higher in both time-frames: (1) in plates precoated with fibronectin in both groups; (2) in P than in C groups. Thus, nerve predegeneration, application of EBM-2 as culture medium and fibronectin as coating appeared a good method for obtaining cultured Schwann cells to be used in different experimental models in rats.
Epidural fibrosis is a frequent complication of lumbar disc surgery, however its influence on incidence of failed back surgeries remains controversial. A bilateral laminectomy (L2–L4) with associated disc injury was performed in 32 adult male Wistar rats. In three experimental groups (n=8 each), spinal cord on laminectomy site was covered with thin layer of gel: alginate, chitosan, or mixture of both. Control group (n=8) was left without treatment. After 4 or 8 weeks, rats (n=4 for each group) were sacrificed and spinal lumbar segments with surrounding muscles were removed and prepared for histologic analysis. Transverse and longitudinal sections were subjected to Masson-Goldner Trichrome staining and examined for severity of epidural fibrosis. Epidural scarring of variable density was found in all laminectomy sites. All experimental groups showed less epidural fibrosis, dural adhesion, fibroblast density, foreign body reaction, and nerve root retraction as compared to the control group. However, no significant differences were found between experimental groups. We suggest that both chitosan and alginate gels form effective barriers for collagen penetration preventing spinal cord from epidural fibrosis following disc injury.
BACKGROUND AND AIMS: Current methods of peripheral nerve cutting are highly unsatisfactory. Imperfect cutting plane directly influences the effect of nerve anastomosis. For precise rejoining of cut nerve stumps directly, or to bridge large gap with autologous nerve graft, the surfaces of nerve stumps must be even and perfectly matching. Actual methods still do not provide such undisturbed pathway for regenerating fibers. In this study, we examined the in situ morphological properties of peripheral nerves cut with an innovative device. METHODS: Rat and rabbit sciatic nerves were cut with the carbonmetal coated blade with bioactive surface mounted on the highspeed dental drill. Transected nerves were subjected to immediate analysis of the plane surface. It was performed using the scanning electron microscope, and standard H-E as well as Masson-trichrome stainings of the serial transverse sections. Analysis was performed by two experienced certified histopathologists. RESULTS: The procedure provided a section area devoid of unevenness or shreds of epineurium or perineurium. Moreover, individual axons seemed to be cut smoothly. The scanning electron microscope images showed the transected axons arranged paralelly to the main axis as well as other undisturbed components of the nerve (i.e. blood vessels and Schwann cells). Also, there was no thermal damage of the cutting plane. CONCLUSION: This technique holds a promise for the development of a minimally invasive alternative approach that utilizes already available technology and equipment, with cutting plane allowing for perfect matching of nerve stumps subjected for rejoining.
We investigated the influence of activated Schwann cells on regeneration of the spinal cord in rats. Young adult male Wistar C rats were used (n=36). Focal injury of spinal cord white matter at Th10 level was produced using our original non-laminectomy method by means of high-pressured air stream. Schwann cells obtained from 7-days-predegenerated rats’ sciatic nerves (n=3) were cultured, transfected with GFP and injected into cisterna magna (S group, n=23) three times: immediately after spinal cord injury and 3 as well as 7 days later (300 000 cells/injection). Control animals (n=10) were subjected to the spinal cord injury only. Neurons in brain stem and motor cortex were labeled with FluoroGold (FG) delivered caudally from the injury site and transported via spinal ascending tracts a week before the end of experiment. Functional outcome (BBB scale, Sciatic Functional Index) and morphological features of regeneration were analyzed during 12-week follow-up. The lesions were characterized by means of MRI. Maximal distance of expansion of implanted cells in the spinal cord was measured and the number of FG-positive neurons was counted. Rats treated with Schwann cells presented significant improvement of locomotor performance when compared to the control group. MR images showed no cyst in the spinal cord in S group, while in the control group changes resembling typical post-traumatic syringomyelia were found. The sizes of lesions were also significantly smaller in S group. Distance covered by Schwann cells was 12 mm from the epicenter of injury. Number of brain stem and motor cortex FG-positive neurons in S group was significantly higher than in control group. Obtained data revealed that activated Schwann cells are able to induce the repair of injured spinal cord white matter. The route of cells application via cisterna magna appeared useful for their delivery into the injury area.
Pierwsza strona wyników Pięć stron wyników wstecz Poprzednia strona wyników Strona / 1 Następna strona wyników Pięć stron wyników wprzód Ostatnia strona wyników
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.