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Brazilian Journal of Medical and Biological Research

versão On-line ISSN 1414-431X

Braz J Med Biol Res v.34 n.10 Ribeirão Preto out. 2001

http://dx.doi.org/10.1590/S0100-879X2001001000013 

Braz J Med Biol Res, October 2001, Volume 34(10) 1325-1329 (Short Communication)

Frequent occurrence of nicotinic acetylcholine receptors in GABAergic neurons of the chick visual system

A.S. Torrão and L.R.G. Britto

Departamento de Fisiologia e Biofísica, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, SP, Brasil

Abstract
Text
References
Acknowledgments
Correspondence and Footnotes


Abstract

Double-labeling immunohistochemical methods were used to investigate the occurrence of the a8 and a5 nicotinic receptor subunits in presumptive GABAergic neurons of the chick nervous system. Nicotinic receptor immunoreactivity was often found in cells exhibiting GABA-like immunoreactivity, especially in the visual system. The a8 subunit appeared to be present in presumptive GABAergic cells of the ventral lateral geniculate nucleus, nucleus of the basal optic root of the accessory optic system, and the optic tectum, among several other structures. The a5 subunit was also found in GABA-positive neurons, as observed in the lentiform nucleus of the mesencephalon and other pretectal nuclei. The numbers of a8- and a5-positive neurons that were also GABA-positive represented high percentages of the total number of neurons containing nicotinic receptor labeling in several brain areas, which indicates that most of the a8 and a5 nicotinic receptor subunits are present in GABAergic cells. Taken together with data from other studies, our results indicate an important role of the nicotinic acetylcholine receptors in the functional organization of GABAergic circuits in the visual system.

Key words: acetylcholine, GABA, neurotransmitters, nicotinic receptors, visual system


Nicotinic acetylcholine receptors (nAChRs) have been reported to be widely distributed in the central nervous system (1,2), where most of them appear to have a modulatory role (3-5). Indeed, several studies have shown a predominance of presynaptic nAChRs in the visual (1,6,7) and other neural systems (5). In addition, several electrophysiological and pharmacological data are suggestive of a modulatory function of nAChRs upon dopaminergic, glutamatergic, noradrenergic (4), and GABAergic (8-14) circuits. As part of a program to chemically identify the central neurons containing nAChRs, we investigated the occurrence of nAChR subunits in presumptive GABAergic neurons of the chick brain by means of double-labeling immunohistochemical techniques. The a8 and a5 nAChR subunits were chosen for this analysis, as they represent different nAChR families (2) and also because monoclonal antibodies (mAb) directed against these two subunits have produced reliable cellular labeling in previous experiments (1,15).

Ten 1-2-week-old chicks (Gallus gallus) were used in the present study. The birds were deeply anesthetized with ketamine and xylazine and perfused through the heart with 0.9% saline and 2% paraformaldehyde (PFA) in 0.1 M phosphate buffer (PB, pH 7.4). The brains were postfixed in 2% PFA for 3-5 h and then transferred to 30% sucrose in PB for cryoprotection. Coronal sections (30 µm) of the frozen brains were cut with a sliding microtome and submitted to immunohistochemical procedures. The brain sections were processed free-floating according to a double-labeling protocol, either with a combination of the rat mAb305 against the a8 nAChR subunit (16) and a guinea pig antiserum against GABA (Eugenetech, Ridgefield Park, NJ, USA), or with a combination of the rat mAb210 against the a5 nAChR subunit (2,17) and the guinea pig antiserum against GABA. All antibodies were diluted 1:250 in PB containing 0.3% Triton X-100. Sections were initially incubated with the mixture of primary antibodies for 14-18 h at room temperature (ca. 22oC). After three washes (15 min each) in PB, the sections were incubated for 1 h at room temperature with a mixture of a goat anti-rat antiserum labeled with rhodamine and a rabbit anti-guinea pig antiserum labeled with fluorescein, both diluted 1:100 in PB. The sections were then washed in PB as described before, mounted on gelatin and chromoalumen-coated slides, and coverslipped with a mixture of carbonate buffer and glycerin. As the antigens studied here are not readily available for preadsorption controls, in some experiments we have omitted the primary antibodies from the procedure or replaced them with normal sera of the same species as the antibodies. Specific staining was completely abolished in both control conditions. The material was analyzed with a fluorescence microscope using the appropriate filters and also with a Zeiss 510 confocal microscope. Double labeling was subjectively evaluated, and cell counts were performed in order to obtain an overall index of co-occurrence of the a8 and a5 nAChR subunits with GABA. These cell counts included only the neurons that stained well above the background, and were performed in at least three sections/animal for each of the structures analyzed here.

The GABA-immunostaining pattern found in the present study for the chick brain was similar to that previously described for the pigeon brain (18), and the patterns of a8 and a5 immunoreactivity agreed well with previous descriptions from our laboratory (1,15). As expected, GABA-immunoreactive cells are much more widely distributed in the chick brain than neurons containing the a8 and a5 nAChR subunits. Double-stained cells containing the a8 subunit of the nAChRs and GABA were found in several structures. These cells were especially frequent in visual system structures, such as the ventral lateral geniculate nucleus (Figure 1), nucleus of the basal optic root of the accessory optic system, and the optic tectum. Some structures exhibited an especially high percentage of a8-positive cells which also contained GABA, such as the subpretectal nucleus (approximately 74%), the ventral lateral geniculate nucleus (about 75%), and the lentiform nucleus of the mesencephalon (ca. 70%). Several structures also exhibited double labeling for the a5 nAChR subunit and GABA, such as the pretectal area, isthmic nucleus, magnocellular portion, and the lentiform nucleus of the mesencephalon (Figure 1). Among the structures that exhibited high percentages of a5-positive cells which also contained GABA are the gray tectal nucleus (100% of the a5-positive cells), the lentiform nucleus of the mesencephalon (approximately 83%), the isthmic nucleus, magnocellular portion (about 90%), and the lateral spiriform nucleus (ca. 80%). The approximate percentages of cholinoceptive neurons (a8- or a5-positive) that contain GABA in several structures of the chick brain are summarized in Table 1. It should be stressed that co-localization of nAChR subunits and GABA was also marked in some non-visual structures, such as the ventral tegmental area and lateral hypothalamus (high numbers of a8/GABA-positive cells), the interpeduncular nucleus (moderate numbers of a8- and a5-positive neurons containing GABA), and the subpretectal nucleus (high numbers of a8/GABA- and a5/GABA-positive cells). Despite the high number of GABA-positive neurons in the chick brain, we could also subjectively estimate the number of presumptive GABAergic neurons containing a8 or a5 nAChR subunits. These numbers were highly variable among structures, ranging from about 5% in the optic tectum to about 90% in the lateral spiriform nucleus and the isthmic nucleus, magnocellular portion. The numbers, however, were very consistent among data from different experiments. The degree of consistency of these numbers was as high as the consistency of the approximate numbers given above for the cholinoceptive neurons containing GABA immunoreactivity.


Figure 1. Digital images of coronal sections of the chick brain through the ventral lateral geniculate nucleus (top) and the lentiform nucleus of the mesencephalon (bottom), taken under rhodamine (a8 and a5) and fluorescein (GABA) microscope filters. The arrows indicate double-labeled neurons and the arrowheads indicate neurons containing only one of the antigens studied. GABA, gamma-aminobutyric acid. Scale bars: 25 µm. Note the greater magnification of the bottom images.

[View larger version of this image (154 K JPG file)]


The data of the present study suggest that many neurons of the chick brain containing both a-bungarotoxin-sensitive (a8) and a-bungarotoxin-insensitive (a5) nAChR subunits (2) also contain GABA immunoreactivity. This indicates that in several chick brain structures the majority of the cholinoceptive neurons are possibly GABAergic. The numbers of cholinoceptive neurons containing GABA in the chick visual system are possibly even higher than those described above, for at least two reasons. First, the immunofluorescence technique is recognizably less sensitive than other immunohistochemical protocols, which suggests that the approximate numbers of double-labeled (nAChR/GABA) neurons given here could actually be higher. Second, we have only tested two nAChR subunits, and the possibility exists that other subunits are also present in GABA-positive neurons. It should be stressed, however, that a5 must assemble with other nAChR subunits in order to generate functional receptors. It is noteworthy that the distribution of the a5 nAChR subunit is similar to the distribution of the ß2 subunit in the chick brain (1,15). The a8 subunits can constitute functional homo-oligomeric receptors, but they may also assemble with a7 subunits in the avian brain (2). In fact, these two subunits of the a-bungarotoxin-sensitive nAChR family co-occur in several visual areas of the chick brain (1).

The frequent occurrence of nAChRs in GABAergic neurons may either represent a morphological substrate for the existence of presynaptic nicotinic receptors which may modulate GABA release, or represent postsynaptic receptors which may directly control the activity of GABAergic cells. The first of these possibilities implies that the existence of nAChR subunits in GABA-positive neurons may mean that these subunits are present in the cell body en route to axon terminals, where they could have a modulatory role (1). In the second case, the staining of perikarya may possibly represent somatic nAChRs, located either on the cell membrane or in the cytoplasm as part of a cytoplasmic receptor pool (2). There are a series of physiological data indicating an effect of nicotinic agonists on the facilitation of GABA release. This effect has been found in the sensory thalamus (11), the rat dorsal motor nucleus of the vagus nerve (9), the hippocampus (8), the ventral lateral geniculate nucleus (10), the lateral spiriform nucleus (14), and cortical interneurons (19). GABAergic axons in these areas should therefore express nicotinic receptors in a terminal or preterminal location, so that these receptors could modulate GABA release. Very little information appears to exist concerning possible postsynaptic effects of nAChRs upon GABAergic neurons. In only one of the structures analyzed here, namely the lateral spiriform nucleus, does a possibility clearly exist of fast postsynaptic nAChRs acting upon GABAergic cells (13). Additional studies are needed to identify the presynaptic or postsynaptic nature of the nAChRs found in GABAergic neurons in this study.

The presence of nAChRs in GABAergic neurons demonstrated here in visual areas of the chick brain does not appear to be limited to that particular neural system. Indeed, the physiological data mentioned above suggest the occurrence of nAChRs in GABAergic neurons in other neural systems and in the brains of other species, including humans (8-11,14,19). Also, the analysis of the extensive maps of the distribution of nAChRs and GABA in the brain of birds and other species (see 1,2,18) reveals that the nicotinic receptor-GABA relationship is likely to extend to the majority of brain areas. Further studies are clearly necessary to evaluate the latter possibility. Interestingly, the a3 nAChR subunit has already been detected in GABAergic perikarya of the chick retina (20). The numbers of cholinoceptive neurons exhibiting the GABA phenotype and the numbers of GABAergic neurons expressing nAChRs both varied according to the retinal area analyzed, reaching almost 40% in both cases (20). Taken together with the latter data in the retina, the present results reveal a close relationship of nAChRs and GABA in the chick visual system and add information about a modulatory role of acetylcholine, acting on nAChRs, in GABAergic circuits.


References

1. Britto LRG, Keyser KT, Lindstrom JM & Karten HJ (1992). Immunohistochemical localization of nicotinic acetylcholine receptor subunits in the mesencephalon and diencephalon of the chick (Gallus gallus). Journal of Comparative Neurology, 317: 325-340.        [ Links ]

2. Lindstrom J (1996). Neuronal nicotinic acetylcholine receptors. In: Narahashi T (Editor), Ion Channels. Plenum Press, New York, 377-450.        [ Links ]

3. MacDermott AB, Role LW & Siegelbaum AS (1999). Presynaptic ionotropic receptors and the control of transmitter release. Annual Review of Neuroscience, 22: 443-485.        [ Links ]

4. Vizi ES & Lendvai B (1999). Modulatory role of presynaptic nicotinic receptors in synaptic and non-synaptic chemical communication in the central nervous system. Brain Research Reviews, 30: 219-235.        [ Links ]

5. Wonnacott S (1997). Presynaptic nicotinic ACh receptors. Trends in Neurosciences, 20: 92-98.        [ Links ]

6. Sargent PB, Pike SH, Nadel DB & Lindstrom JM (1989). Nicotinic acetylcholine receptor-like molecules in the retina, retinotectal pathway, and optic tectum of the frog. Journal of Neuroscience, 9: 565-573.        [ Links ]

7. Swanson LW, Simmons DM, Whiting PJ & Lindstrom J (1987). Immunohistochemical localization of neuronal nicotinic receptors in the rodent central nervous system. Journal of Neuroscience, 7: 3334-3342.        [ Links ]

8. Alkondon M, Pereira EFR, Barbosa CTF & Albuquerque EX (1997). Neuronal nicotinic receptor activation modulates gamma-aminobutyric acid release from CA1 neurons of rat hippocampal slices. Journal of Pharmacology and Experimental Therapeutics, 283: 1396-1411.        [ Links ]

9. Bertolino M, Kellar KJ, Vicini S & Gillis RA (1997). Nicotinic receptor mediates spontaneous GABA release in the rat dorsal motor nucleus of the vagus. Neuroscience, 79: 671-681.        [ Links ]

10. Guo JZ, Tredway TL & Chiappinelli VA (1998). Glutamate and GABA release are enhanced by different subtypes of presynaptic nicotinic receptors in the lateral geniculate nucleus. Journal of Neuroscience, 18: 1963-1969.        [ Links ]

11. Léna C & Changeux JP (1997). Role of Ca2+ ions in nicotinic facilitation of GABA release in mouse thalamus. Journal of Neuroscience, 17: 576-585.        [ Links ]

12. Lu Y, Grady S, Marks MJ, Picciotto M, Changeux JP & Collins AC (1998). Pharmacological characterization of nicotinic receptor-stimulated GABA release from mouse brain synaptosomes. Journal of Pharmacology and Experimental Therapeutics, 287: 648-657.        [ Links ]

13. Nong Y, Sorenson EM & Chiappinelli VA (1999). Fast excitatory nicotinic transmission in the chick lateral spiriform nucleus. Journal of Neuroscience, 19: 7804-7811.        [ Links ]

14. Zhu PJ & Chiappinelli VA (1999). Nicotine modulates evoked GABAergic transmission in the brain. Journal of Neurophysiology, 82: 3041-3045.        [ Links ]

15. Torrão AS, Lindstrom JM & Britto LRG (1997). Distribution of the a2, a3, and a5 nicotinic acetylcholine receptor subunits in the chick brain. Brazilian Journal of Medical and Biological Research, 30: 1209-1213.        [ Links ]

16. Schoepfer R, Conroy WG, Whiting P, Gore M & Lindstrom J (1990). Brain a-bungarotoxin binding protein cDNAs and mAbs reveal subtypes of this branch of the ligand-gated ion channel gene superfamily. Neuron, 5: 35-48.        [ Links ]

17. Conroy WG, Vernallis AB & Berg DK (1992). The a5 gene product assembles with multiple acetylcholine receptor subunits to form distinctive receptor subtypes in brain. Neuron, 9: 679-691.        [ Links ]

18. Veenman CL & Reiner A (1994). The distribution of GABA-containing perikarya, fibers, and terminals in the forebrain and midbrain of pigeons, with particular reference to the basal ganglia and its projection targets. Journal of Comparative Neurology, 339: 209-250.        [ Links ]

19. Alkondon M, Pereira EFR, Eisenberg HM & Albuquerque EX (2000). Nicotinic receptor activation in human cerebral cortical interneurons: a mechanism for inhibition and disinhibition of neuronal networks. Journal of Neuroscience, 20: 66-75.        [ Links ]

20. Hamassaki-Britto DE, Brzozowska-Prechtl A, Karten HJ, Lindstrom JM & Keyser KT (1991). GABA-like immunoreactive cells containing nicotinic acetylcholine receptors in the chick retina. Journal of Comparative Neurology, 313: 394-408.        [ Links ]


Acknowledgments

Thanks are due to Dr. Jon M. Lindstrom, University of Pennsylvania, for his kind donation of monoclonal antibodies against nicotinic receptor subunits.


Correspondence and Footnotes

Address for correspondence: A.S. Torrão, Departamento de Fisiologia e Biofísica, ICB, USP, Av. Prof. Lineu Prestes, 1524, 05508-900 São Paulo, SP, Brasil. Fax: +55-11-3818-7426. E-mail: andrea@fisio.icb.usp.br

Research supported by FAPESP, CNPq and PRONEX/MCT. A.S. Torrão was the recipient of a postdoctoral fellowship from FAPESP. Received April 4, 2001. Accepted August 2, 2001.

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