Tendon chitosan tubes covalently coupled with synthesized laminin peptides facilitate nerve regeneration in vivo

2003 ◽  
Vol 72 (5) ◽  
pp. 646-659 ◽  
Author(s):  
Masumi Suzuki ◽  
Soichiro Itoh ◽  
Isamu Yamaguchi ◽  
Kazuo Takakuda ◽  
Hisatoshi Kobayashi ◽  
...  
Keyword(s):  
Nerve Regeneration ◽  
Laminin Peptides

Hydroxyapatite-coated tendon chitosan tubes with adsorbed laminin peptides facilitate nerve regeneration in vivo

2003 ◽  
Vol 993 (1-2) ◽  
pp. 111-123 ◽  
Author(s):  
Soichiro Itoh ◽  
Isamu Yamaguchi ◽  
Masumi Suzuki ◽  
Shizuko Ichinose ◽  
Kazuo Takakuda ◽  
...  
Keyword(s):  
Nerve Regeneration ◽  
Laminin Peptides

The effect of Rho Kinase inhibition on corneal nerve regeneration in vitro and in vivo

2021 ◽  
Author(s):  
Sonja Mertsch ◽  
Inga Neumann ◽  
Cosima Rose ◽  
Marc Schargus ◽  
Gerd Geerling ◽  
...  
Keyword(s):  
Nerve Regeneration ◽  
Rho Kinase ◽  
Kinase Inhibition ◽  
Corneal Nerve ◽  
Regeneration In Vitro

Nerve branching is induced and oriented by a small applied electric field

1990 ◽  
Vol 95 (4) ◽  
pp. 605-615
Author(s):  
C.D. McCaig
Keyword(s):  
Electric Field ◽  
Dimethyl Sulfoxide ◽  
Nerve Regeneration ◽  
Applied Electric Field ◽  
Large Majority ◽  
Ganglioside Gm1 ◽  
Pharmacological Agents ◽  
Extrinsic Cues

Nerve branching is controlled by intrinsic and extrinsic cues, one of which may be a small applied electric field. Lateral processes were induced by passing current through a micropipette placed at 90 degrees to the shaft of a developing nerve. The appearance of processes was a polarised event with a large majority arising from the cathodal facing side of nerves. Whilst an electric field alone may promote branching, the presence of dimethyl sulfoxide (DMSO) or the ganglioside GM1 enhanced branching of developing nerves. It is likely that an applied electric field promotes microtubule disassembly locally along the neurite shaft and that this can lead to a polarised rearrangement of the neuronal cyto-skeleton. It is suggested that the use of an applied electric field in conjunction with these pharmacological agents might enhance nerve regeneration in vivo.

scholarly journals 3D Printed Polymeric Hydrogels for Nerve Regeneration

Polymers ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 1041 ◽  
Author(s):  
Binoy Maiti ◽  
David Díaz Díaz
Keyword(s):  
Nerve Regeneration ◽  
Nerve Cell ◽  
Clinical Applications ◽  
Cell Regeneration ◽  
3D Bioprinting ◽  
Ability To Regenerate ◽  
3D Printed ◽  
Polymeric Hydrogels ◽  
Human Nervous System

The human nervous system lacks an inherent ability to regenerate its components upon damage or diseased conditions. During the last decade, this has motivated the development of a number of strategies for nerve regeneration. However, most of those approaches have not been used in clinical applications till today. For instance, although biomaterial-based scaffolds have been extensively used for nerve reparation, the lack of more customized structures have hampered their use in vivo. This highlight focuses mainly on how 3D bioprinting technology, using polymeric hydrogels as bio-inks, can be used for the development of new nerve guidance channels or devices for peripheral nerve cell regeneration. In this concise contribution, some of the most recent and representative examples are highlighted to discuss the challenges involved in various aspects of 3D bioprinting for nerve cell regeneration, specifically when using polymeric hydrogels.

scholarly journals Motor Nerve Regeneration Using an Optimized Nerve Allograft in a Rat Model - An In vitro and In vivo Analysis

2015 ◽  
Vol 40 (9) ◽  
pp. e35
Author(s):  
Caroline A. Hundepool ◽  
Liselotte F. Bulstra ◽  
Dimitra Kotsougiani ◽  
Steven Hovius ◽  
Allen Bishop ◽  
...  
Keyword(s):  
Nerve Regeneration ◽  
Rat Model ◽  
Motor Nerve ◽  
In Vivo Analysis

Nerve regeneration model and trophic factors in vivo

1982 ◽  
Vol 232 (1) ◽  
pp. 157-161 ◽  
Author(s):  
Göran Lundborg ◽  
Frank M. Longo ◽  
Silvio Varon
Keyword(s):  
Nerve Regeneration ◽  
Trophic Factors

scholarly journals In Vivo Confocal Microscopy Evaluation in Patients with Keratoconus

2022 ◽  
Vol 11 (2) ◽  
pp. 393
Author(s):  
Alvin Wei Jun Teo ◽  
Hassan Mansoor ◽  
Nigel Sim ◽  
Molly Tzu-Yu Lin ◽  
Yu-Chi Liu
Keyword(s):  
Confocal Microscopy ◽  
Nerve Regeneration ◽  
Nerve Fibre ◽  
Ex Vivo ◽  
Fibre Length ◽  
In Vivo Confocal Microscopy ◽  
Corneal Sensitivity ◽  
Mechanical Removal ◽  
Cellular Changes

Keratoconus is the most common primary corneal ectasia characterized by progressive focal thinning. Patients experience increased irregular astigmatism, decreased visual acuity and corneal sensitivity. Corneal collagen crosslinking (CXL), a minimally invasive procedure, is effective in halting disease progression. Historically, keratoconus research was confined to ex vivo settings. In vivo confocal microscopy (IVCM) has been used to examine the corneal microstructure clinically. In this review, we discuss keratoconus cellular changes evaluated by IVCM before and after CXL. Cellular changes before CXL include decreased keratocyte and nerve densities, disorganized subbasal nerves with thickening, increased nerve tortuosity and shortened nerve fibre length. Repopulation of keratocytes occurs up to 1 year post procedure. IVCM also correlates corneal nerve status to functional corneal sensitivity. Immediately after CXL, there is reduced nerve density and keratocyte absence due to mechanical removal of the epithelium and CXL effect. Nerve regeneration begins after 1 month, with nerve fibre densities recovering to pre-operative levels between 6 months to 1 year and remains stable up to 5 years. Nerves remain tortuous and nerve densities are reduced. Corneal sensitivity is reduced immediately postoperatively but recovers with nerve regeneration. Our article provides comprehensive review on the use of IVCM imaging in keratoconus patients.

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