1995
DOI: 10.1017/s0952523800007276
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Synaptic circuitry of serotonin-synthesizing and serotonin-accumulating amacrine cells in the retina of the cane toad, Bufo marinus

Abstract: The synaptic connections of amacrine cells synthesizing or accumulating serotonin in the retina of the cane toad, Bufo marinus, were studied by using preembedding double-labeling electron-microscopic immunocytochemistry. The binding sites of an anti-serotonin antibody were revealed by the diaminobenzidine reaction, whilst a colloidal gold-conjugated secondary antibody was used to detect an antibody to phenylalanine hydroxylase. Since the latter antibody recognizes tryptophan 5-hydroxylase, one of the synthesiz… Show more

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Cited by 7 publications
(8 citation statements)
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“…Our findings are consistent with the notion that some types of bipolar cells accumulate serotonin in different vertebrate retinas (Witkovsky et al. 1984; Zhu et al. 1992, 1995; Gabriel et al.…”
Section: Discussionsupporting
confidence: 93%
“…Our findings are consistent with the notion that some types of bipolar cells accumulate serotonin in different vertebrate retinas (Witkovsky et al. 1984; Zhu et al. 1992, 1995; Gabriel et al.…”
Section: Discussionsupporting
confidence: 93%
“…Possible postsynaptic elements are the serotonin immunoreactive amacrines of Xenopus which receive input from bipolars mostly in SLs 2 and 5 of the IPL. Serotonin synthesizing amacrines in Bufo were also found to receive input from bipolar cells but the peak of the distribution is in SL3 Zhu et al, 1995) where the direct bipolar to ganglion cell contacts are few. GABA immunoreactivity appears in about 50% of the amacrine cells in Bufo and they are postsynaptic to bipolar cells.…”
Section: Cell Types Possibly Involved and Functional Considerationsmentioning
confidence: 98%
“…The strips were rinsed in PBS containing 0.1% BSA, followed by a rinse in 50% ethanol in distilled water for 10 min to facilitate antibody penetration (Llewellyn-Smith et al, 1992). The combined treatment of 1% sodium borohydride with washing in 50% ethanol significantly enhanced the penetration of antibody (Zhu et al, 1995), but either treatment alone had less effect. Retinal strips were initially incubated in 0.6% hydrogen peroxide in PBS for 30 min; blocked in 10% HS, 10% RS, and 5% BSA in PBS without Triton X-100 for 1 h; and subsequently incubated with 192-IgG (1:50, Oncogene) for about 72 h at 4°C.…”
Section: Pre-embedding Immunoelectron Microscopymentioning
confidence: 99%