Aminergic and Indoleamine Accumulating Neurons in the Retina of the River Lamprey (Lampetra fluviatilis)

Tissues were processed for fluorescence microscopy of biogenic amines according to the method of Falck and Hillarp. Normal animals, and animals injected with α-methylnoradrenaline or 5,6-dihydroxytryptamine were used. Catecholamine containing neurons (junctional cells) occur in the innermost rows of cell bodies of the inner nuclear layer (INL) and close to the vitreous surface. Catecholamine containing fibers occur in three layers: (1) an outer layer around the innermost perikarya of the INL, which is a condition not found in retinas of gnathostome chordates; (2) a middle layer within the outer third of the inner synaptic layer (ISL), separated from the outer layer by ganglion cell axons; (3) a sparse inner layer within the innermost third of the ISL. A few catecholamine containing fibers were seen to extend from the innermost region of the INL to the outer synaptic layer. The position of the junctional cells in the lamprey corresponds to that in gnathostome chordates, but whereas all catecholamine containing fiber layers in gnathostomes are located sclerally to the optic fiber layer and within the ISL, the middle and the inner fiber layers in the lamprey occur vitreally to the optic fiber layer. Indoleamine accumulating neurons occur in the innermost row of perikarya of the INL and close to the vitreous surface. Those of the INL send fine, varicose branches to the ISL forming a network which is somewhat denser at the inner and outer borders of the ISL than in its middle. The indoleamine accumulating terminals do not ramify within the INL in contrast to the catecholamine containing terminals.

[1]  K. Holmberg,et al.  ERG-recordings from the retina of the river lamprey (Lampetra fluviatilis) , 1977, Vision Research.

[2]  Peter Öhman Fine structure of photoreceptors and associated neurons in the retina of Lampetra fluviatilis (Cyclostomi) , 1976, Vision Research.

[3]  B. Ehinger CHAPTER 7 – BIOGENIC MONOAMINES AS TRANSMITTERS IN THE RETINA , 1976 .

[4]  B. Boycott,et al.  Interplexiform cells of the mammalian retina and their comparison with catecholamine-containing retinal cells , 1975, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[5]  B Ehinger,et al.  Synaptic organization of the amine-containing interplexiform cells of the goldfish and Cebus monkey retinas. , 1975, Science.

[6]  L. Iversen Uptake mechanisms for neurotransmitter amines. , 1974, Biochemical pharmacology.

[7]  A. Laties,et al.  An indoleamine-containing cell in chick retina. , 1973, Investigative Ophthalmology.

[8]  A. Björklund,et al.  Cytofluorometry of Biogenic Monoamines in the Falck-Hillarp Method. Structural Identification by Spectral Analysis , 1973 .

[9]  Y. Sano,et al.  Fluorescence microscopic observations on the dog retina. , 1968, Archivum histologicum Japonicum = Nihon soshikigaku kiroku.

[10]  D. Jacobowitz,et al.  The influence of light and dark on the catecholamine content of the retina and choroid. , 1967, Investigative ophthalmology.

[11]  D. Jacobowitz,et al.  A comparative study of the autonomic innervation of the eye in monkey, cat, and rabbit , 1966, The Anatomical record.

[12]  J. Häggendal,et al.  IDENTIFICATION AND CELLULAR LOCALIZATION OF THE CATECHOLAMINES IN THE RETINA AND THE CHOROID OF THE RABBIT. , 1965, Acta physiologica Scandinavica.

[13]  C. Owman,et al.  A DETAILED METHODOLOGICAL DESCRIPTION OF THE FLUORESCENCE METHOD FOR THE CELLULAR DEMONSTRATION OF BIOGENIC MONOAMINES , 1965 .

[14]  T. Malmfors,et al.  EVIDENCE OF DOPAMINE-CONTAINING NEURONS IN THE RETINA OF RABBITS. , 1963, Acta physiologica Scandinavica.