메뉴 건너뛰기




Volumn 60, Issue 3, 1999, Pages 3239-3243

Nonlinear transfer function encodes synchronization in a neural network from the mammalian brain

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; BRAIN; HIPPOCAMPUS; NERVE CELL NETWORK; NEWBORN; PATHOLOGY; PHYSIOLOGY; RABBIT;

EID: 0033200637     PISSN: 1063651X     EISSN: None     Source Type: Journal    
DOI: 10.1103/PhysRevE.60.3239     Document Type: Article
Times cited : (9)

References (49)
  • 12
    • 85036252452 scopus 로고    scopus 로고
    • The stimulation protocol was established at the beginning of every experiment. The stimulus amplitude was kept constant at the minimal value able to produce a synaptic response (known as postsynaptic potential). Ten to twenty trials of repetitive stimulation from 0 to 20 Hz were tested
    • The stimulation protocol was established at the beginning of every experiment. The stimulus amplitude was kept constant at the minimal value able to produce a synaptic response (known as postsynaptic potential). Ten to twenty trials of repetitive stimulation from 0 to 20 Hz were tested.
  • 13
    • 85036245247 scopus 로고    scopus 로고
    • Transverse slices of hippocampus from newborn rats and rabbits (2–5 postnatal days), 500 μm in thickness, were prepared using a drop-blade chopper. For recording, one slice was transferred to a submerged-type recording chamber (Medical Systems) continuously perfused with the standard perfusion medium (in mM: 125 NaCl, 3 KCl, 1.2 (Formula presented) 1.2 (Formula presented) 2 (Formula presented) 22 (Formula presented) and 10 glucose, saturated with 95% (Formula presented) (Formula presented) pH: 7.4). Recording electrodes were made from borosilicate glass (outer diameter, 1.2 mm, Sutter Instrument Co.) pulled with a Brown-Flaming horizontal puller (Sutter Instrument Co.), and filled with 3M KCl (50–100 MΩ). Simultaneous intracellular recordings were made with separated manipulators using a dual intracellular amplifier (Axoclamp II B). Monopolar electrical stimulation was applied via tungsten electrodes at mossy fibers simultaneously with intracellular recordings. The stimulus duration was 100 μs. See 8 for more details on the stimulation protocol
    • Transverse slices of hippocampus from newborn rats and rabbits (2–5 postnatal days), 500 μm in thickness, were prepared using a drop-blade chopper. For recording, one slice was transferred to a submerged-type recording chamber (Medical Systems) continuously perfused with the standard perfusion medium (in mM: 125 NaCl, 3 KCl, 1.2 (Formula presented) 1.2 (Formula presented) 2 (Formula presented) 22 (Formula presented) and 10 glucose, saturated with 95% (Formula presented) (Formula presented) pH: 7.4). Recording electrodes were made from borosilicate glass (outer diameter, 1.2 mm, Sutter Instrument Co.) pulled with a Brown-Flaming horizontal puller (Sutter Instrument Co.), and filled with 3M KCl (50–100 MΩ). Simultaneous intracellular recordings were made with separated manipulators using a dual intracellular amplifier (Axoclamp II B). Monopolar electrical stimulation was applied via tungsten electrodes at mossy fibers simultaneously with intracellular recordings. The stimulus duration was 100 μs. See 8 for more details on the stimulation protocol.
  • 21
    • 0023986221 scopus 로고
    • Long-term potentiation (LTP) is a mechanism by which repetitive stimulation of a fiber enhances its excitatory synaptic contacts. It has been proposed to be a form of memory; see R. A. Nicoll, J. A. Kauer, and R. C. Malenka, Neuron 1, 97 (1988)
    • (1988) Neuron , vol.1 , pp. 97
    • Nicoll, R.A.1    Kauer, J.A.2    Malenka, R.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.