The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Afferent connections of the laterodorsal and the pedunculopontine tegmental nuclei in the rat: A retro‐ and antero‐grade transport and immunohistochemical study
Abstract
Increasingly strong evidence suggests that cholinergic neurons in the mesopontine tegmentum play important roles in the control of wakefulness and sleep. To understand better how the activity of these neurons is regulated, the potential afferent connections of the laterodorsal (LDT) and pedunculopontine tegmental nuclei (PPT) were investigated in the rat. This was accomplished by using retrograde and anterograde axonal transport methods and NADPH‐diaphorase histochemistry. Immunohistochemistry was also used to identify the transmitter content of some of the retrogradely identified afferents. Following injections of the retrograde tracer wheatgerm agglutinin‐conjugated horseradish peroxidase (WGA‐HRP) into either the LDT or the PPT, labelled neurons were seen in a number of limbic forebrain structures. The medial prefrontal cortex and lateral habenula contained more retrogradely labelled neurons from the LDT, whereas in the bed nucleus of the stria terminalis and central nucleus of the amygdala, more cells were labelled from the PPT. Moderate numbers of neurons were seen in the magnocellular regions of the basal forebrain, and many labelled neurons were observed in the lateral hypothalamus, the zona incerta, and the midbrain central gray from both the LDT and the PPT. Accessory oculomotor nuclei in the midbrain as well as eye movement‐related structures in the lower brainstem contained some neurons labelled from the LDT, and fewer neurons from the PPT. A few labelled neurons were seen in somatosensory and other sensory relay nuclei in the brainstem and the spinal cord. Retrograde labelling was seen in a number of extrapyramidal structures, including the globus pallidus, entopenduncular and subthalamic nuclei, and substantia nigra following PPT injections; with LDT injections, labelling was similar in density in the substantia nigra but virtually absent in the entopeduncular and subthalamic nuclei. Data with the fluorescent retrograde tracer fluorogold combined with immunofluorescence indicated that many neurons in the zona incerta‐lateral hypothalamic region that were retrogradely labelled from the LDT contained α‐melanocyte‐stimulating hormone. Numerous neurons were labelled throughout the reticular formation of the brainstem following either LDT or PPT injections. Many neurons retrogradely labelled in the LDT and PPT, the dorsal and median raphe nuclei, and the locus ceruleus contained choline acetyltransferase, serotonin, and tyrosine hydroxylase, respectively. The anterograde tracers WGA‐HRP and phaseolus vulgaris leucoagglutinin were used to confirm some of the projections indicated by the retrograde labelling data; anterograde labelling was seen in the LDT and PPT following injections of one of these tracers into the medial prefrontal cortex, lateral hypothalamus, and the contralateral LDT. NADPH‐diaphorase histochemistry combined with immunohistochemistry indicated that serotonin and tyrosine hydroxylase‐immunoreactive fibers bearing occasional swellings were closely associated with NADPH‐diaphorase‐positive, cholinergic neurons in the LDT and PPT. These data suggest that potential afferents to the LDT and the PPT arise in many common, but also some separate structures in the forebrain, brainstem, and spinal cord. Both the LDT and the PPT appear to receive heavy inputs from three structures: brainstem reticular formation, midbrain central gray, and lateral hypothalamus‐zona incerta region. Other, less prominent afferents originate in a number of limbic, oculomotor, extrapyramidal, and sensory structures, with some degrees of preference for the LDT or PPT. Some of the reticular connections with the LDT and PPT are serotoninergic or noradrenergic. The reticuloreticular network also includes commissural and rostrocaudal cholinergic interconnections between the LDT and PPT. The apparent similarities in both the afferent and efferent connections of the LDT and the PPT are consistent with the working hypothesis that cholinergic neurons in the mesopontine tegmentum represent a single functional unit. The potential afferent connections identified in the present study also suggest that the PPT and LDT are involved in the regulation of behavioral state. © 1992 Wiley‐Liss, Inc.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Jones, B. E., & Yang, T. (1985) · Journal of Comparative Neurology · doi:10.1002/cne.902420105 · Cited by 896
Kayama, Y., Ohta, M., & Jodo, E. (1992) · Brain Research · doi:10.1016/0006-8993(92)90632-j · Cited by 247
REM sleep burst neurons, PGO waves, and eye movement information.
Nelson, J. P., McCarley, R. W., & Hobson, J. A. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.50.4.784 · Cited by 190
Cited by
The hippocampal-VTA loop: controlling the entry of information into long-term memory
Lisman, J. E., & Grace, A. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.002 · Cited by 1,983
Control of sleep and wakefulness
Brown, R. E., Basheer, R., McKenna, J. T., Strecker, R. E., & McCarley, R. W. (2012) · Physiological Reviews · doi:10.1152/physrev.00032.2011 · Cited by 1,477
Dreaming and the brain: toward a cognitive neuroscience of conscious states
Hobson, J. A., Pace-Schott, E. F., & Stickgold, R. (2000) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00003976 · Cited by 985
Heidbreder, C. A., & Groenewegen, H. J. (2003) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2003.09.003 · Cited by 882
The reinterpretation of dreams: An evolutionary hypothesis of the function of dreaming
Revonsuo, A. (2000) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00004015 · Cited by 676
Metadata
- Authors
- Semba, K., & Fibiger, H. C.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1992-09-15
- Volume
- 323
- Issue
- 3
- Pages
- 387-410
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2042593835
- Cited by
- 543
- References
- 3
- FWCI
- 6.26
- Type
- journal article
- Language
- en
- Open access
- closed
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
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Afferent connections of the laterodorsal and the pedunculopontine tegmental nuclei in the rat: A retro‐ and antero‐grade transport and immunohistochemical study. https://app.cochat.ai/papers/10.1002/cne.903230307
- The paper
- Semba, K., & Fibiger, H. C. (1992). Afferent connections of the laterodorsal and the pedunculopontine tegmental nuclei in the rat: A retro‐ and antero‐grade transport and immunohistochemical study. Journal of Comparative Neurology. https://doi.org/10.1002/cne.903230307
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.