The DOI matches its Crossref record; 99 of the 99 references it cites were found in a registry or an index.
Projections of the medial preoptic nucleus: A Phaseolus vulgaris leucoagglutinin anterograde tract‐tracing study in the rat
Abstract
The projections of the medial preoptic nucleus (MPN) were examined by making injections of the anterogradely transported lectin Phaseolus vulgaris leucoagglutinin (PHA‐L) into the MPN and charting the distribution of labeled fibers. The evidence indicates that the MPN projects extensively to widely distributed regions in both the forebrain and brainstem, most of which also supply inputs to the nucleus. An important neuroendocrine role for the MPN is underscored by its extensive projections to almost all parts of the periventricular zone of the hypothalamus, including the anteroventral periventricular, anterior part of the periventricular, paraventricular (PVH), and arcuate nuclei, and a role in autonomic mechanisms is indicated by projections to such regions as the dorsal and lateral parvicellular parts of the PVH, the lateral parabrachial nucleus, and the nucleus of the solitary tract. Other projections of the MPN suggest participation in the initiation of specific motivated behaviors. For example, inputs to two nuclei of the medial zone of the hypothalamus, the ventromedial and dorsomedial nuclei, may be related to the control of reproductive and ingestive behaviors, respectively, although the possible functional significance of a strong projection to the ventral premammillary nucleus is presently unclear. The execution of these behaviors may involve activation of somatomotor regions via projections to the substantia innominata, zona incerta, ventral tegmental area, and pedunculopontine nucleus. Similarly, inputs to other regions that project directly to the spinal cord, such as the periaqueductal gray, the laterodorsal tegmental nucleus, certain medullary raphe nuclei, and the magnocellular reticular nucleus may also be involved in modulating somatic and/or autonomic reflexes. Finally, the MPN may influence a wide variety of physiological mechanisms and behaviors through its massive projections to areas like the ventral part of the lateral septal nucleus, the bed nucleus of the stria terminalis, the lateral hypothalamic area, the supramammillary nucleus, and the ventral tegmental area, all of which have extensive connections with regions along the medial forebrain bundle. Although the PHA‐L method does not allow a clear demonstration of possible differential projections from each subdivision of the MPN, our results suggest that each of them does give rise to a unique pattern of outputs. This pattern of projections was found to be essentially the same in female rats and appears to be unique to the MPN, since injections of PHA‐L into the lateral preoptic or anterior hypothalamic areas, or into other nuclei within the medial preoptic area showed quite different patterns of outputs.
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
Hsu, S. M., Raine, L., & Fanger, H. (1981) · Journal of Histochemistry & Cytochemistry · doi:10.1177/29.4.6166661 · Cited by 14,140
Hypothalamic integration: organization of the paraventricular and supraoptic nuclei
Swanson, L. W., & Sawchenko, P. E. (1983) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.06.030183.001413 · Cited by 1,991
Self-citationSwanson, L. W. (1982) · Brain Research Bulletin · doi:10.1016/0361-9230(82)90145-9 · Cited by 1,718
Self-citationAtlas of estradiol‐concentrating cells in the central nervous system of the female rat
Pfaff, D., & Keiner, M. (1973) · Journal of Comparative Neurology · doi:10.1002/cne.901510204 · Cited by 1,494
Swanson, L. W., & Kuypers, H. G. J. M. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901940306 · Cited by 1,413
Self-citationAnnals of the New York Academy of Sciences
(2019) · Annals of the New York Academy of Sciences · doi:10.1111/(issn)1749-6632 · Cited by 1,305
Evidence for a morphological sex difference within the medial preoptic area of the rat brain
Gorski, R. A., Gordon, J. H., Shryne, J. E., & Southam, A. M. (1978) · Brain Research · doi:10.1016/0006-8993(78)90723-0 · Cited by 1,227
Gerfen, C. R., & Sawchenko, P. E. (1984) · Brain Research · doi:10.1016/0006-8993(84)90940-5 · Cited by 1,199
The connections of the septal region in the rat
Swanson, L. W., & Cowan, W. M. (1979) · Journal of Comparative Neurology · doi:10.1002/cne.901860408 · Cited by 1,135
Self-citationSubnuclear organization of the efferent connections of the parabrachial nucleus in the rat
Fulwiler, C. E., & Saper, C. B. (1984) · Brain Research Reviews · doi:10.1016/0165-0173(84)90012-2 · Cited by 918
Cited by
Simerly, R. B., Swanson, L. W., Chang, C., & Muramatsu, M. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.902940107 · Cited by 2,118
Self-citationNEWMAN, S. W. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09271.x · Cited by 1,189
Cerebral hemisphere regulation of motivated behavior
Swanson, L. W. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02905-x · Cited by 846
Self-citationEfferent projections of the infralimbic cortex of the rat
Hurley, K. M., Herbert, H., Moga, M. M., & Saper, C. B. (1991) · Journal of Comparative Neurology · doi:10.1002/cne.903080210 · Cited by 777
Sherin, J. E., Elmquist, J. K., Torrealba, F., & Saper, C. B. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-12-04705.1998 · Cited by 746
Metadata
- Authors
- Simerly, R. B., & Swanson, L. W.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1988-04-08
- Volume
- 270
- Issue
- 2
- Pages
- 209-242
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2075236615
- Cited by
- 592
- References
- 99
- FWCI
- 10.27
- 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: Projections of the medial preoptic nucleus: A Phaseolus vulgaris leucoagglutinin anterograde tract‐tracing study in the rat. https://app.cochat.ai/papers/10.1002/cne.902700205
- The paper
- Simerly, R. B., & Swanson, L. W. (1988). Projections of the medial preoptic nucleus: A Phaseolus vulgaris leucoagglutinin anterograde tract‐tracing study in the rat. Journal of Comparative Neurology. https://doi.org/10.1002/cne.902700205
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.