Cited by 8

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Structures mediating cholinergic reticular facilitation of cortical responses in the cat: effects of lesions in immunocytochemically characterized projections

Müller, C. M., Lewandowski, M. H., Singer, W.·1993·Experimental Brain Research

Abstract

Cholinergic afferents to the neocortex controlled by the mesencephalic reticular formation (MRF) are known to transiently facilitate cortical excitability. In an attempt to identify the pathway mediating this effect in the cat visual cortex we combined retrograde tracing techniques with immunocytochemical methods to visualize the acetylcholine-synthesizing enzyme choline acetyltransferase (ChAT). In addition we examined, in acute electrophysiological experiments, whether local neurotoxin injections into nuclei of the basal forebrain interfered with the reticular facilitation of cortical evoked potentials. Cholinergic projections to area 17 originate from different centers in the homolateral substantia innominata/internal capsule, the septal nuclei, and the nuclei of the diagonal band of Broca. No direct cholinergic projection from the MRF to the visual cortex was observed. Retrogradely labelled cells intermingled with ChAT-positive neurons in the brainstem generally revealed immunopositivity for catecholaminergic markers. Local injections of neurotoxins in the substantia innominata blocked reticular facilitation, whereas local lesions of the septal nuclei and the nuclei of the diagonal band had no effect on MRF-induced facilitation. The blockage of the reticular facilitation of cortical evoked responses after unilateral lesions of the substantia innominata was bilateral, suggesting a cooperative interaction between basal forebrain structures of the two hemispheres. The anatom…

Overview

Integrity signals

Registry

Crossref · 10.1007/bf00230434

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

Research works printed but not linked: 47

  1. Bear MF, Singer W (1986) Modulation of visual cortical plasticity by acetylcholine and noradrenaline. Nature 320:172–176 · DOI · Paper page
  2. Bear MF, Carnes KM, Ebner FF (1985) An investigation of cholinergic circuitry in cat striate cortex using acetylcholinesterase histochemistry. J Comp Neurol 234:411–430 · DOI
  3. Bentivoglio M, Macchi G, Rossini P, Tempesta E (1978) Brain stem neurons projecting to neocortex: an HRP study in the cat. Exp Brain Res 31:489–498 · DOI
  4. Boylan MK, Fisher RS, Hull CD, Buchwald NA, Levine MS (1986) Axonal branching of basal forebrain projections to the neocortex: a double-labeling study in the cat. Brain Res 375:176–181 · DOI
  5. Buzsáki G, Bickford RG, Ponomareff G, Thal LJ, Mandel R, Gage FH (1988) Nucleus basalis and thalamic control of neocortical activity in the freely moving rat. J Neurosci 8:4007–4026 · DOI · Paper page
  6. Divac I (1975) Magnocellular nuclei of the basal forebrain project to neocortex, brain stem, and olfactory bulb. Review of some functional correlates. Brain Res 93:385–398 · DOI
  7. Edwards SB, Olmos JS de (1976) Autoradiographic studies of the projections of the midbrain reticular formation: ascending projections of nucleus cuniformis. J Comp Neurol 165:417–432 · DOI
  8. Fisher RS, Buchwald NA, Hull CD, Levine MS (1988) GABAergic basal forebrain neurons project to the neocortex: the localization of glutamic acid decarboxylase and choline acetyltransferase in feline corticopetal neurons. J Comp Neurol 272:489–502 · DOI
  9. Francesconi W, Müller CM, Singer W (1988) Cholinergic mechanisms in the reticular control of transmission in the cat lateral geniculate nucleus. J Neurophysiol 59:1690–1718 · DOI
  10. Henderson Z (1987) Source of cholinergic input to ferret visual cortex. Brain Res 412:261–268 · DOI
  11. Johnston MV, Young AC, Coyle, JT (1981) Laminar distribution of cholinergic markers in neocortex: effects of lesions. J Neurosci Res 6:597–607 · DOI
  12. Jones BE, Beaudet A (1987a) Retrograde labeling of neurons in the brainstem following injections of [3H]choline into the forebrain of the rat. Exp Brain Res 65:437–448
  13. Jones BE, Beaudet A (1987b) Distribution of acetylcholine and catecholamine neurons in the cat brainstem: a choline acetyltransferase and tyrosine hydroxylase immunohistochemical study. J Comp Neurol 261:15–32 · DOI
  14. Katz LC, Burkhalter A, Dreyer WJ (1984) Fluorescent latex microspheres as a retrograde neuronal marker for in vivo and in vitro studies of visual cortex. Nature 310:498–500 · DOI
  15. Krnjevic K, Pumain R, Renaud L (1971) The mechanism of excitation by acetylcholine in the cerebral cortex. J Physiol (Lond) 215:247–268 · DOI
  16. Lamour Y, Dutar P, Jobert A (1984) Cortical projections of the nucleus of the diagonal band of Broca and of the substantia innominata in the rat: an anatomical study using the anterograde transport of a conjugate of wheat germ agglutinin and horseradish peroxidase. Neuroscience 12:395–408 · DOI
  17. Lewandowski M, Müller CM, Singer W (1993) Reticular facilitation of cat visual cortical responses is mediated by nicotinic and muscarinic cholinergic mechanisms. Exp Brain Res 96:1–7 · DOI
  18. Lima AD de, Singer W (1987) The brainstem projection to the lateral geniculate nucleus in the cat: identification of cholinergic and monoaminergic elements. J Comp Neurol 259:92–121 · DOI
  19. McCormick DA, Prince DA (1986) Mechanisms of action of acetylcholine in the guinea pig cerebral cortex, in vitro. J Physiol (Lond) 375:169–194 · DOI · Paper page
  20. McDonald JW, Silverstein FS, Johnston MV (1988) Neurotoxicity of N-methyl-d-aspartate is markedly enhanced in developing rat central nervous system. Brain Res 459:200–203 · DOI
  21. Metherate R, Weinberger NM (1989) Acetylcholine produces stimulus specific receptive-field alterations in cat auditory cortex. Brain Res 480:372–377 · DOI
  22. Metherate R, Tremblay N, Dykes RW (1987) Acetylcholine permits long-term enhancement of neuronal responsiveness in cat primary somatosensory cortex. Neuroscience 1:75–81 · DOI
  23. Mitchell SJ, Richardson RT, Baker FH, De Long MR (1987) The primate nucleus basalis of Meynert: neuronal activity related to a visuomotor tracking task. Exp Brain Res 68:506–515
  24. Moruzzi G, Magoun HW (1949) Brainstem reticular formation and activation of the EEG. Electroencephalogr Clin Neurophysiol 1:455–473 · DOI · Paper page
  25. Müller CM, Singer W (1989) Acetylcholine-induced inhibition in the cat visual cortex is mediated by a GABAergic mechanism. Brain Res 487:335–342 · DOI
  26. Nistri A, Bartolini A, Deffenu G, Pepeu G (1972) Investigations into the release of acetylcholine from the cerebral cortex of the cat: effects of amphetamine, of scopolamine and of septal lesions. Neuropharmacology 11:665–674 · DOI
  27. Pearson RCA, Neal JW, Powell TPS (1986) Hypertrophy of cholinergic neurones of the basal nucleus in the rat following damage of the contralateral nucleus. Brain Res 382:149–152 · DOI
  28. Price JL, Stern R (1983) Individual cells in the nucleus basalis-diagonal band complex have restricted axonal projections to the cerebral cortex in the rat. Brain Res 269:352–356 · DOI
  29. Prusky GT, Shaw C, Cynader MS (1988) The distribution and ontogenesis of [3H]nicotine binding sites in cat visual cortex. Brain Res Dev Brain Res 39:161–176 · DOI
  30. Richardson RT, De Long MR (1986) Nucleus basalis of Meynert neuronal activity during a delayed response task in monkey. Brain Res 399:364–368 · DOI
  31. Sato H, Hata Y, Hagihara K, Tsumoto T (1987a) Effects of cholinergic depletion on neuron activities in the cat visual cortex. J Neurophysiol 58:781–794 · DOI
  32. Sato H, Hata Y, Masui H, Tsumoto T (1987b) A functional role of cholinergic innervation to neurons in the cat visual cortex. J Neurophysiol 58:765–780 · DOI · Paper page
  33. Semba K, Reiner PB, McGeer EG, Fibinger HC (1988a) Noncholinergic basal forebrain neurons project to the contralateral basal forebrain in the rat. Neurosci Lett 84:23–28 · DOI
  34. Semba K, Reiner PB, McGeer EG, Fibinger HC (1988b) Brainstem afferents to the magnocellular basal forebrain studied by axonal transport, immunohistochemistry, and electrophysiology in the rat. J Comp Neurol 267:433–453 · DOI
  35. Shaw C, Needler MC, Cynader M (1984) Ontogenesis of muscarinic acetylcholine binding sites in cat visual cortex: reversal of specific laminar distribution during the critical period. Brain Res Dev Brain Res 14:295–299 · DOI
  36. Singer W (1977) Control of thalamic transmission by corticofugal and ascending reticular pathways in the visual system. Physiol Rev 57:386–420 · DOI
  37. Singer W (1979) Central-core control of visual cortex functions. In: Schmitt FO, Worden FG (eds) The neurosciences fourth study program, MIT, Cambridge, Mass., pp 1093–1110
  38. Steriade M, Biesold D (eds) (1990) Brain cholinergic systems, Oxford University Press, Oxford
  39. Stewart DJ, MacFabe DF, Vanderwolf CH (1984) Cholinergic activation of the electrocorticogram: role of the substantia innominata and effects of atropine and quinuclidinyl benzilate. Brain Res 322:219–232 · DOI
  40. Stichel CC, Singer W (1985) Organization and morphological characteristics of choline acetyltransferase-containing fibers in the visual thalamus and striate cortex of the cat. Neurosci Lett 53:155–160 · DOI
  41. Stichel CC, Singer W (1987) Quantitative analysis of the choline acetyltransferase-immunoreactive axonal network in the cat primary visual cortex. I. Adult cats. J Comp Neurol 258:91–98 · DOI
  42. Swanson LW (1976) An autoradiographic study of the efferent conections of the preoptic region in the rat. J Comp Neurol 167:227–256 · DOI · Paper page
  43. Tomimoto H, Kamo H, Kameyama M, McGeer P, Kimura H (1987) Descending projections of the basal forebrain in the rat demonstrated by the anterograde neural tracer Phaseolus vulgaris leucoagglutinin (PHA-L). Brain Res 425:248–255 · DOI
  44. Vanderwolf CH (1987) Near-total loss of ‘learning’ and ‘memory’ as a result of combined cholinergic and serotonergic blockade in the rat. Behav Brain Res 23:43–57 · DOI
  45. Vertes RP (1988) Brainstem afferents to the basal forebrain in the rat. Neuroscience 24:907–935 · DOI
  46. Vincent SR, Reiner PB (1987) The immunohistochemical localization of choline acetyltransferase in the cat brain. Brain Res Bull 18:371–415 · DOI
  47. Wahle P, Sanides-Buchholtz C, Eckenstein F, Albus K (1984) Concurrent visualization of choline acetyltransferase like immunoreactivity and retrograde transport of neocortically injected markers in basal forebrain neurons of cat and rat. Neurosci Lett 44:223–228 · DOI

Cited by

Sorted by citations

See all 8

Metadata

Authors
Müller, C. M., Lewandowski, M. H., & Singer, W.
Venue
Experimental Brain Research
Published
1993-09
Volume
96
Issue
1
Pages
8-18
ISSN
  • 0014-4819
  • 1432-1106
Cited by
8
References
1
Language
en

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review