A method for generating precise temporal patterns of retinal spiking using prosthetic stimulation

被引:181
作者
Fried, SI
Hsueh, HA
Werblin, FS
机构
[1] Univ Calif Berkeley, Dept Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Vis Sci, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Bioengn & Mol, Berkeley, CA 94720 USA
关键词
D O I
10.1152/jn.00849.2005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The goal of retinal prosthetic devices is to generate meaningful visual information in patients that have lost outer retinal function. To accomplish this, these devices should generate patterns of ganglion cell activity that closely resemble the spatial and temporal components of those patterns that are normally elicited by light. Here, we developed a stimulus paradigm that generates precise temporal patterns of activity in retinal ganglion cells, including those patterns normally generated by light. Electrical stimulus pulses (>= 1-ms duration) elicited activity in neurons distal to the ganglion cells; this resulted in ganglion cell spiking that could last as long as 100 ms. However, short pulses, < 0.15 ms, elicited only a single spike within 0.7 ms of the leading edge of the pulse. Trains of these short pulses elicited one spike per pulse at frequencies <= 250 Hz. Patterns of short electrical pulses ( derived from normal light elicited spike patterns) were delivered to ganglion cells and generated spike patterns that replicated the normal light patterns. Finally, we found that one spike per pulse was elicited over almost a 2.5:1 range of stimulus amplitudes. Thus a common stimulus amplitude could accommodate a 2.5: 1 range of activation thresholds, e. g., caused by differences arising from cell biophysical properties or from variations in electrode-to-cell distance arising when a multielectrode array is placed on the retina. This stimulus paradigm can generate the temporal resolution required for a prosthetic device.
引用
收藏
页码:970 / 978
页数:9
相关论文
共 34 条
[1]   A MODEL FOR ELECTRCAL STIMULATION OF CENTRAL MYELINATED FIBERS WITH MONOPOLAR ELECTRODES [J].
BEMENT, SL ;
RANCK, JB .
EXPERIMENTAL NEUROLOGY, 1969, 24 (02) :171-+
[2]   ELECTRICAL-STIMULATION WITH PT ELECTRODES .2. ESTIMATION OF MAXIMUM SURFACE REDOX (THEORETICAL NON-GASSING) LIMITS [J].
BRUMMER, SB ;
TURNER, MJ .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 1977, 24 (05) :440-443
[3]   PREVALENCE OF RETINITIS PIGMENTOSA IN MAINE [J].
BUNKER, CH ;
BERSON, EL ;
BROMLEY, WC ;
HAYES, RP ;
RODERICK, TH .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1984, 97 (03) :357-365
[4]   The artificial silicon retina microchip for the treatment of vision loss from retinitis pigmentosa [J].
Chow, AY ;
Chow, VY ;
Packo, KH ;
Pollack, JS ;
Peyman, GA ;
Schuchard, R .
ARCHIVES OF OPHTHALMOLOGY, 2004, 122 (04) :460-469
[5]   In vitro comparison of the charge-injection limits of activated iridium oxide (AIROF) and platinum-iridium microelectrodes [J].
Cogan, SF ;
Troyk, PR ;
Ehrlich, J ;
Plante, TD .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2005, 52 (09) :1612-1614
[6]  
Curcio CA, 1996, INVEST OPHTH VIS SCI, V37, P1236
[7]   Directional selectivity is formed at multiple levels by laterally offset inhibition in the rabbit retina [J].
Fried, SI ;
Münch, TA ;
Werblin, FS .
NEURON, 2005, 46 (01) :117-127
[8]   Mechanisms and circuitry underlying directional selectivity in the retina [J].
Fried, SI ;
Münch, TA ;
Werblin, FS .
NATURE, 2002, 420 (6914) :411-414
[9]  
Friedman DS, 2004, ARCH OPHTHALMOL-CHIC, V122, P564
[10]  
GREENBERG RJ, 1998, THESIS J HOPKINS U