Intracellular Ca2+ and adaptation of voltage responses to light in Hermissenda photoreceptors
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Muzzio, IA
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Rutgers State Univ, Dept Psychol, Program Biopsychol & Behav Neurosci, New Brunswick, NJ 08902 USARutgers State Univ, Dept Psychol, Program Biopsychol & Behav Neurosci, New Brunswick, NJ 08902 USA
Muzzio, IA
[1
]
Talk, AC
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Rutgers State Univ, Dept Psychol, Program Biopsychol & Behav Neurosci, New Brunswick, NJ 08902 USARutgers State Univ, Dept Psychol, Program Biopsychol & Behav Neurosci, New Brunswick, NJ 08902 USA
Talk, AC
[1
]
Matzel, LD
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Rutgers State Univ, Dept Psychol, Program Biopsychol & Behav Neurosci, New Brunswick, NJ 08902 USARutgers State Univ, Dept Psychol, Program Biopsychol & Behav Neurosci, New Brunswick, NJ 08902 USA
Matzel, LD
[1
]
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[1] Rutgers State Univ, Dept Psychol, Program Biopsychol & Behav Neurosci, New Brunswick, NJ 08902 USA
FLUORESCENT imaging of Ca2+ and intracellular recordings were used to assess Ca2+ increases and voltage responses during light presentations in Hermissenda B photoreceptors. Ca2+ levels increased and were sustained during a relatively long exposure to light. Repeated presentations of a brief light induced an elevation of intracellular Ca2+ that persisted throughout short inter-light intervals, but which dissipated during long inter-light intervals. In all instances, the magnitude of the intracellular Ca2+ signal was inversely related to the amplitude of the light-induced generator potential. Blocking of voltage-dependent Ca2+ channels did not significantly affect the magnitude of the Ca2+ signal, suggesting that the intracellular Ca2+ response arises primarily from release from intracellular stores. These results indicate that Ca2+ plays an important role in the modulation of the voltage responses to light, acting to suppress the response during repetitive or prolonged stimulation. (C) 1998 Rapid Science Ltd.