Summary
The effects of microelectrophoretically applied melatonin (aMT), 5-methoxytryptophol (ML), 5-hydroxytryptophol (HL) and noradrenaline (NA) on the electrical activity of cerebellar Purkinje and other cells during both day- and nighttime were studied in urethane-anesthetized intact and pinealectomized homing pigeons and guinea pigs.
In the intact pigeon, equal numbers of Purkinje cells were excited and inhibited by aMT and ML, whilst the responses to HL were predominantly inhibitory. The responses varied significantly depending on whether the cells were tested during the day or at night (P<0.001). Pinealectomy abolished the observed day/night differences. In intact pigeons most of the other cerebellar units were inhibited by aMT and ML, whilst HL elicited an excitation in about 50% of the units.
In the guinea pig most of the Purkinje cells were inhibited by aMT and ML, whereas HL caused no response in most of the units. No significant 24-h rhythmicity in response to the indoles could be observed. The responses of the other cerebellar units were more complicated. aMT caused an excitation in most of the units, whilst the predominant response caused by ML was inhibition. Only 30% of these units responded to HL; the remainder showed no measurable responses.
It is apparent from these studies that pineal indoleamines may play a modulatory role in the cerebellum.
Similar content being viewed by others
Abbreviations
- ECG :
-
electrocardiogram
- GABA :
-
gamma-aminobutyric acid
References
Aschoff J, Daan S, Groos GA (1982) Vertebrate circadian systems. Structure and physiology. Springer, Berlin Heidelberg New York
Bloom FE, Hoffer BJ, Siggins GR, Barker JL, Nicoll RA (1972) Effects of serotonin on central neurons: Microiontophoretic administration. Fed Proc 31:97–106
Brown G, Grota L, Bubenik G, Niles L, Tsui H (1981) Physiologic regulation of melatonin. In: Birau N, Schloot W (eds) Melatonin, current status and perspectives. Adv Biosci 29:95–112
Bubenik GA, Brown GM, Uhlir I, Grota LJ (1974) Immunohistological localization of N-acetylindolalkylamines in pineal gland, retina and cerebellum. Brain Res 81:233–242
Carter SJ, Laud CA, Smith I, Leone RM, Hooper RJL, Silman RE, Finnie MDA, Mullen PE, Larson-Carter DL (1979) Concentration of 5-methoxytryptophol in pineal gland and plasma of the rat. J Endocrinol 83:35–40
Chan-Palay V (1977) Cerebellar dentate nucleus. Organization, cytology and transmitters. Springer, Berlin Heidelberg New York
Cohen M, Roselle D, Chabner B, Schmidt TJ, Lippman M (1978) Evidence for a cytoplasmic melatonin receptor. Nature 274:894–895
Crepel F, Dhanjal SS (1981) Sensitivity of Purkinje cell dendrites to glutamate and aspartate in cerebellar slices maintained in vitro. J Physiol 320:54P
Demaine C, Kann HC (1979) Modification of electrical activity of hypothalamic neurones by pineal indoles. Progr Brain Res 52:373–375
Eccles JC, Ito M, Szentágothai J (1967) The cerebellum as a neuronal machine. Springer, Berlin Heidelberg New York
Freedman R, Hoffer BJ, Puro D, Woodward DJ (1976) Noradrenaline modulation of the responses of the cerebellar Purkinje cell to afferent synaptic activity. Br J Pharmacol 57:603–605
Freedman R, Hoffer BJ, Woodward DJ, Puro D (1977) A functional role for the adrenergic input to the cerebellar cortex: interaction of norepinephrine with activity evoked by mossy and climbing fibers. Exp Neurol 55:269–288
Fuxe K, Johnsson G (1974) Further mapping of central 5-hydroxytryptamine neurons: Studies with the neurotoxic dihydroxytryptamines. Adv Biochem Pharmacol 10:1–12
Gaston S, Menaker M (1968) Pineal function: The biological clock in the sparrow. Science 160:1125–1127
Gwinner E, Benzinger I (1978) Synchronisation of a circadian rhythm in pinealectomized European starlings by daily injections of melatonin. J Comp Physiol 127:209–213
Harnischfeger G (1979) An improved method for extracellular marking of electrode tips in nervous tissue. J Neurosci Meth 1:195–200
Hökfelt T, Fuxe K (1969) Cerebellar monoamine nerve terminals, a new type of afferent fibers to the cortex cerebelli. Exp Brain Res 9:63–72
Hoffer BJ, Siggins GR, Bloom FE (1969) Response of single cerebellar Purkinje (P) cells to microelectrophoresis by norepinephrine (NE) and serotonin (5-MT). Fed Proc 28:443
Hoffer BJ, Siggins GR, Oliver AP, Bloom FE (1973) Activation of the pathway from locus coeruleus to rat cerebellar Purkinje neurons: Pharmacological evidence of noradrenergic central inhibition. J Pharmacol Exp Ther 184:553–569
Lerner AB, Case JD, Takahashi Y, Lee Y, Mori W (1958) Isolation of melatonin, the pineal gland factor that lightens melanocytes. J Am Chem Soc 80:2587
McGeer PL, Eccles JC, McGeer EG (1978) Molecular neurobiology of the mammalian brain. Plenum Press, New York London
McLaughlin BJ, Wood JG, Saito K, Barber R, Vaughn JE, Roberts E, Wu J-Y (1974) The fine structural localization of glutamate decarboxylase in synaptic terminals of rodent cerebellum. Brain Res 76:377–391
Menaker M, Zimmerman N (1976) Role of the pineal in the circadian system of birds. Am Zool 16:45–55
Moises HC, Woodward DJ, Hoffer BJ, Freedman R (1979) Interactions of norepinephrine with Purkinje cell responses to putative amino acid neurotransmitters applied by microiontophoresis. Exp Neurol 64:493–515
Moises HC, Waterhouse BD, Woodward DJ (1981) Locus coeruleus stimulation potentiates Purkinje cell responses to afferent input: The climbing fiber system. Brain Res 222:43–64
Müller U, Heinsen H (1984) Regional differences in the ultrastructure of Purkinje cells of the rat. Cell Tissue Res 235:91–98
Niles LP, Wong Y-W, Misra RK, Brown GM (1979) Melatonin receptors in brain. Eur J Pharmacol 55:219–220
Palkovits M, Brownstein M, Saavedra JM (1974) Serotonin content of the brain stem nuclei in the rat. Brain Res 80:237–249
Pévet P (1983) Is 5-methoxytryptamine a pineal hormone? Psychoneuroendocrinol 8:61–73
Quay WB (1968) Individuation and lack of pineal effect in the rat's circadian locomotor activity. Physiol Behav 3:109–118
Quay WB (1974) Pineal chemistry. Charles C Thomas, Springfield, Ill
Ralph CL, Pelham RW, MacBride SE, Reilly DP (1974) Persistent rhythms of pineal and serum melatonin in cockerels in continuous darkness. J Endocrinol 63:319–324
Ralph CL, Binkley S, MacBride SE, Klein DC (1975) Regulation of pineal rhythms in chickens: effects of blinding, constant light, constant dark, and superior cervical ganglionectomy. Endocrinology 97:1373–1378
Reiter RJ (1981) The pineal gland. Anatomy and biochemistry, vol 1. CRC Press, Boca Raton, Florida
Sailinger-Holle R, Vollrath L (1980) Pineal structure and wheelrunning activity in rats. Physiol Behav 25:985–987
Semm P (1981) Electrophysiological aspects of the mammalian pineal gland. In: Oksche A, Pévet P (eds) The pineal organ: Photobiology-biochronometry-endocrinology. Developments in endocrinology, vol 14, Elsevier/North-Holland, Amsterdam New York Oxford, pp 81–96
Semm P (1983) Neurobiological investigations of the pineal gland and its hormone melatonin. In: Axelrod J, Fraschini F, Velo GP (eds) Pineal and its endocrine role. Plenum Press, New York London, pp 437–465
Semm P, Vollrath L (1982) Alterations in the spontaneous activity of cells in the guinea pig pineal gland and visual system produced by pineal indoles. J Neural Transm 53:265–275
Semm P, Demaine C, Vollrath L (1981a) Electrical responses of pineal cells to melatonin and putative transmitters. Evidence for circadian changes in sensitivity. Exp Brain Res 43:361–370
Semm P, Demaine C, Vollrath L (1981b) Electrical responses of pineal cells to thyroid hormones and parathormone: a microelectrophoretic study. Neuroendocrinology 33:212–217
Szabadi E (1979) Adrenoceptors on central neurones: Microelectrophoretic studies. Neuropharmacology 18:831–843
Vollrath L (1981) The pineal organ. In: Oksche A, Vollrath L (eds) Handbuch der mikroskopischen Anatomie des Menschen, vol 6, Part 7. Springer, Berlin Heidelberg New York, pp 1–665
Waldhauser F, Wurtman RJ (1983) The secretion and actions of melatonin. In: Litwack G (ed) Biochemical actions of hormones, vol 10. Academic Press, New York, pp 187–225
Wilkinson M, Arendt J, Bradtke J, De Ziegler D (1977) Determination of a dark-induced increase of pineal N-acetyl transferase activity and simultaneous radioimmunoassay of melatonin in pineal, serum and pituitary tissue of the male rat. J Endocrinol 72:243–244
Yeh HH, Moises HC, Waterhouse BD, Woodward DJ (1981) Modulatory interactions between norepinephrine and taurine, beta-alanine, gamma-aminobutyric acid and muscimol, applied iontophoretically to cerebellar Purkinje cells. Neuropharmacology 20:549–560
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Semm, P., Vollrath, L. Electrical responses of homing pigeon and guinea pig Purkinje cells to pineal indoleamines applied by microelectrophoresis. J. Comp. Physiol. 154, 675–681 (1984). https://doi.org/10.1007/BF01350221
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF01350221