» Articles » PMID: 7226202

Pineal Complex of the Clawed Toad, Xenopus Laevis Daud.: Structure and Function

Overview
Journal Cell Tissue Res
Date 1981 Jan 1
PMID 7226202
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

The morphological and physiological properties of the pineal complex of Xenopus laevis were investigated in larval, juvenile and adult animals. In a representative majority of adult X. laevis, the frontal organ does not display signs of degeneration. Fully differentiated frontal organs contain photoreceptors typical of the pineal complex of lower vertebrates. By means of the acetylcholinesterase (AChE)-reaction approximately 30 neurons of two different types were demonstrated in the frontal organ. The frontal-organ nerve is composed of approximately 10 myelinated and 40 unmyelinated nerve fibers. The neuropil areas of the frontal organ are generally similar to the corresponding structures of the intracranial epiphysis. The neuronal apparatus of the epiphysis cerebri of X. laevis consists of (i) photoreceptor cells, (ii) approximately 100 AChE-positive neurons, (iii) complex neuropil areas, and (iv) a pineal tract formed by approximately 10 myelinated and approximately 100 unmyelinated nerve fibers. Some of them exhibit granular inclusions indicating that pinealopetal elements may enter the pineal complex of X. laevis via this pathway. The topography of the pineal tract of X. laevis differs considerably from that in ranid species. The most conspicuous element of the plexiform zones is the ribbon synapse. The basal processes of the photoreceptor cells may be presynaptic elements of simple, tangential, dyad or triad synaptic contacts. Conventional synapses were observed only occasionally. Electrophysiological recordings revealed that the pineal complex of Xenopus laevis is directly sensitive to light. In response to light stimuli, two types of responses, achromatic and chromatic, were recorded from the nerve of the frontal organ. In contrast, the epiphysis exhibited only achromatic units. The opposed color mechanism of the chromatic response showed a maximum sensitivity at approximately 360 nm for the inhibitory and at 520 nm for the excitatory event. The action spectrum of the achromatic response of the epiphysis and the frontal organ peaked between 500 and 520 nm and showed no Purkinje-shift during dark adaptation. The functional significance of these phenomena is discussed.

Citing Articles

Photoneuroendocrine, circadian and seasonal systems: from photoneuroendocrinology to circadian biology and medicine.

Korf H Cell Tissue Res. 2024; .

PMID: 39264444 DOI: 10.1007/s00441-024-03913-7.


Type II Opsins in the Eye, the Pineal Complex and the Skin of : Using Changes in Skin Pigmentation as a Readout of Visual and Circadian Activity.

Bertolesi G, Debnath N, Malik H, Man L, McFarlane S Front Neuroanat. 2022; 15:784478.

PMID: 35126061 PMC: 8814574. DOI: 10.3389/fnana.2021.784478.


Chromatic clocks: Color opponency in non-image-forming visual function.

Spitschan M, Lucas R, Brown T Neurosci Biobehav Rev. 2017; 78:24-33.

PMID: 28442402 PMC: 5510539. DOI: 10.1016/j.neubiorev.2017.04.016.


Spontaneous magnetic alignment behaviour in free-living lizards.

Diego-Rasilla F, Perez-Mellado V, Perez-Cembranos A Naturwissenschaften. 2017; 104(3-4):13.

PMID: 28251303 DOI: 10.1007/s00114-017-1439-7.


Diversification of non-visual photopigment parapinopsin in spectral sensitivity for diverse pineal functions.

Koyanagi M, Wada S, Kawano-Yamashita E, Hara Y, Kuraku S, Kosaka S BMC Biol. 2015; 13:73.

PMID: 26370232 PMC: 4570685. DOI: 10.1186/s12915-015-0174-9.


References
1.
Omura Y, Ali M . Responses of pineal photoreceptors in the brook and rainbow trout. Cell Tissue Res. 1980; 208(1):111-22. DOI: 10.1007/BF00234177. View

2.
Diederen J . A possible functional relationship between the subcommissural organ and the pineal complex and lateral eyes in Rana esculenta and Rana temporaria. Cell Tissue Res. 1975; 158(1):37-60. DOI: 10.1007/BF00219950. View

3.
Paul E, Hartwig H, Oksche A . [Neurons and central nervous connections of the pineal organ in Anura]. Z Zellforsch Mikrosk Anat. 1971; 112(4):466-93. View

4.
Oksche A, VAUPEL-VON HARNACK M . [Electron microscopic studies on the nerve tracts of the pineal complex of Rana esculenta L]. Z Zellforsch Mikrosk Anat. 1965; 68(3):389-426. View

5.
Eldred W, Finger T, Nolte J . Central projections of the frontal organ of Rana pipiens, as demonstrated by the anterograde transport of horseradish peroxidase. Cell Tissue Res. 1980; 211(2):215-22. DOI: 10.1007/BF00236444. View