Long-Term Functionality of Transversal Intraneural Electrodes Is Improved by Dexamethasone Treatment

被引:18
作者
de la Oliva, N. [1 ,2 ]
del Valle, J. [1 ,2 ,3 ,4 ]
Delgado-Martinez, I. [1 ,2 ]
Mueller, M. [5 ]
Stieglitz, T. [5 ,6 ,7 ]
Navarro, Xavier [1 ,2 ,8 ]
机构
[1] Univ Autonoma Barcelona, Inst Neurosci, Dept Cell Biol Physiol & Immunol, E-08193 Barcelona, Spain
[2] Ctr Invest Biomed Red Enfermedades Neurodegenerat, Madrid 28031, Spain
[3] CSIC, Catalan Inst Nanotechnol ICN2, Campus UAB, Bellaterra 08193, Spain
[4] BIST, Campus UAB, Bellaterra, Spain
[5] Albert Ludwigs Univ Freiburg, Lab Biomed Microtechnol, Dept Microsyst Engn IMTEK, D-79085 Freiburg, Germany
[6] Albert Ludwigs Univ Freiburg, BrainLinks BrainTools Cluster Excellence, D-79085 Freiburg, Germany
[7] Albert Ludwigs Univ Freiburg, Bernstein Ctr Freiburg, D-79085 Freiburg, Germany
[8] Univ Autonoma Barcelona, Fac Med, E-08193 Barcelona, Spain
关键词
Dexamethasone; foreign body reaction; intraneural electrode; neuroprosthesis; stimulation; FOREIGN-BODY REACTION; RELEASE; TISSUE; MICROELECTRODES; INTERFACE; RESPONSES; IMPLANT; DEVICES; TIME;
D O I
10.1109/TNSRE.2019.2897256
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Neuroprostheses aimed to restore lost functions after a limb amputation are based on the interaction with the nervous system by means of neural interfaces. Among the different designs, intraneural electrodes implanted in peripheral nerves represent a good strategy to stimulate nerve fibers to send sensory feedback and to record nerve signals to control the prosthetic limb. However, intraneural electrodes, as any device implanted in the body, induce a foreign body reaction (FBR) that results in the tissue encapsulation of the device. The FBR causes a progressive decline of the electrode functionality over time due to the physical separation between the electrode active sites and the axons to the interface. Modulation of the inflammatory response has arisen as a good strategy to reduce the FBR and maintain electrode functionality. In this paper, transversal intraneural multi-channel electrodes (TIMEs) were implanted in the rat sciatic nerve and tested for three months to evaluate stimulation and recording capabilities under chronic administration of dexamethasone. Dexamethasone treatment significantly reduced the threshold for evoking muscle responses during the follow-up compared to saline-treated animals, without affecting the selectivity of stimulation. However, dexamethasone treatment did not improve the signal-to-noise ratio of the recorded neural signals. Dexamethasone treatment allowed to maintain more working active sites along time than saline treatment. Thus, systemic administration of dexamethasone appears as a useful treatment in chronically implanted animals with neural electrodes as it increases the number of functioning contacts of the implanted TIME and reduces the intensity needed to stimulate the nerve.
引用
收藏
页码:457 / 464
页数:8
相关论文
共 41 条
[1]   Foreign body reaction to biomaterials [J].
Anderson, James M. ;
Rodriguez, Analiz ;
Chang, David T. .
SEMINARS IN IMMUNOLOGY, 2008, 20 (02) :86-100
[2]  
[Anonymous], 2009, 1099312018 ISO, V3
[3]   Spatial and Functional Selectivity of Peripheral Nerve Signal Recording With the Transversal Intrafascicular Multichannel Electrode (TIME) [J].
Badia, Jordi ;
Raspopovic, Stanisa ;
Carpaneto, Jacopo ;
Micera, Silvestro ;
Navarro, Xavier .
IEEE TRANSACTIONS ON NEURAL SYSTEMS AND REHABILITATION ENGINEERING, 2016, 24 (01) :20-27
[4]   Biocompatibility of Chronically Implanted Transverse Intrafascicular Multichannel Electrode (TIME) in the Rat Sciatic Nerve [J].
Badia, Jordi ;
Boretius, Tim ;
Pascual-Font, Aran ;
Udina, Esther ;
Stieglitz, Thomas ;
Navarro, Xavier .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2011, 58 (08) :2324-2332
[5]   Comparative analysis of transverse intrafascicular multichannel, longitudinal intrafascicular and multipolar cuff electrodes for the selective stimulation of nerve fascicles [J].
Badia, Jordi ;
Boretius, Tim ;
Andreu, David ;
Azevedo-Coste, Christine ;
Stieglitz, Thomas ;
Navarro, Xavier .
JOURNAL OF NEURAL ENGINEERING, 2011, 8 (03)
[6]   Prospects of common biomolecules as coating substances for polymeric biomaterials [J].
Balaji, A. ;
Jaganathan, S. K. ;
Vellayappan, M. V. ;
John, A. A. ;
Subramanian, A. P. ;
SelvaKumar, M. ;
Mohandas, H. ;
Raj, Sundar M. ;
Supriyanto, Eko .
RSC ADVANCES, 2015, 5 (85) :69660-69679
[7]   N Methods for Implant Acceptance and Wound Healing: Material Selection and Implant Location Modulate Macrophage and Fibroblast Phenotypes [J].
Boddupalli, Anuraag ;
Zhu, Lida ;
Bratlie, Kaitlin M. .
ADVANCED HEALTHCARE MATERIALS, 2016, 5 (20) :2575-2594
[8]   A transverse intrafascicular multichannel electrode (TIME) to interface with the peripheral nerve [J].
Boretius, Tim ;
Badia, Jordi ;
Pascual-Font, Aran ;
Schuettler, Martin ;
Navarro, Xavier ;
Yoshida, Ken ;
Stieglitz, Thomas .
BIOSENSORS & BIOELECTRONICS, 2010, 26 (01) :62-69
[9]   Actively controlled release of Dexamethasone from neural microelectrodes in a chronic in vivo study [J].
Buehler, C. ;
Kleber, C. ;
Martini, N. ;
Xie, Y. ;
Dryg, I. ;
Stieglitz, T. ;
Hofmann, U. G. ;
Asplund, M. .
BIOMATERIALS, 2017, 129 :176-187
[10]   Extracellular matrix-based materials for neural interfacing [J].
Chen, Shuodan ;
Allen, Mark G. .
MRS BULLETIN, 2012, 37 (06) :606-613