Histamine: putative transmitter for lateral inhibition in Limulus eye.
Histamine: putative transmitter for lateral inhibition in Limulus eye.
复制标题
组胺:鲎眼中横向抑制的推定递质。
DOI:
10.1086/bblv193n2p203
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发表时间:
1997
期刊:
影响因子:
--
通讯作者:
Barlow,RB
中科院分区:
文献类型:
--
作者:
Stewart,KM;Porcello,DM;McSweeney,ME;Saito,T;Passaglia,CL;Dodge,FA;Barlow,RB
Lateral inhibition is an integrative mechanism found in many nervous systems. In retinas, it enhances borders and edges in the visual field (1). Since its discovery in the lateral eye of the horseshoe crab, Limulus polyphemus, by H. Keffer Hartline and colleagues in 1952 (2), lateral inhibition has been studied extensively (3). It is now the foundation of a comprehensive model of retinal function (4). One question, however, remains unanswered. What is the neurotransmitter that mediates lateral inhibition in the Limulus eye? Histamine has been implicated as a photoreceptor neurotransmitter in Uniramia and Crustacea, two of the major groups of arthropods (5, 6, 7). In preparations that study the postsynaptic effects of histamine, histamine has been shown to be inhibitory (7, 8). Biochemical studies show that histamine and the enzymes that synthesize it are present in the Limulus retina (9), but provide no physiological evidence that histamine is the transmitter of lateral inhibition. In this paper, we report electrophysiological and pharmacological studies that test the role of histamine in lateral inhibition in the Limulus eye.In the first experiment, we tested whether histamine mimics the action of lateral inhibition on optic nerve activity generated by eccentric cells in individual ommatidia. To gain access to eccentric cells, we excised the lateral eye and sectioned it into three or four slices. One slice was placed in a Lucite perfusion chamber (volume 0.5 ml). A glass microelectrode filled with 3 h4 KC1 (25 MR) was connected to a DC bridge amplifier (Electronics Shop, Rockefeller University) and advanced into an ommatidium using a Burleigh Inchworm (Burleigh Instruments, Fishers, NY) attached to a manipulator. A fiber optic light pipe was aligned with the optical axis of the ommatidium for maximal stimulation. In this manner, we recorded intracellular responses of eccentric cells to 8-s light flashes delivered every 5 min. After a series of control runs in which a modified Limulus Ringer was perfused over the slice (rate: 1 ml/min), a 1 mM solution of histamine in saline was applied to the slice at the same rate.