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Prefrontal cortex afferents to the anterior temporal lobe in the Macaca fascicularis monkey
ABSTRACT The anatomical organization of the lateral prefrontal cortex (LPFC) afferents to the anterior part of the temporal lobe (ATL) remains to be clarified. The LPFC has two subdivisions, dorsal (dLPFC) and ventral (vLPFC), which have been linked to cognitive processes. The ATL includes several d...
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Published in: | Journal of comparative neurology (1911) 2015-12, Vol.523 (17), p.2570-2598 |
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creator | Mohedano-Moriano, Alicia Muñoz-López, Mónica Sanz-Arigita, Ernesto Pró-Sistiaga, Palma Martínez-Marcos, Alino Legidos-Garcia, María Ester Insausti, Ana María Cebada-Sánchez, Sandra Arroyo-Jiménez, María Del Mar Marcos, Pilar Artacho-Pérula, Emilio Insausti, Ricardo |
description | ABSTRACT
The anatomical organization of the lateral prefrontal cortex (LPFC) afferents to the anterior part of the temporal lobe (ATL) remains to be clarified. The LPFC has two subdivisions, dorsal (dLPFC) and ventral (vLPFC), which have been linked to cognitive processes. The ATL includes several different cortical areas, namely, the temporal polar cortex and rostral parts of the perirhinal, inferotemporal, and anterior tip of the superior temporal gyrus cortices. Multiple sensory modalities converge in the ATL. All of them (except the rostral inferotemporal and superior temporal gyrus cortices) are components of the medial temporal lobe, which is critical for long‐term memory processing. We studied the LPFC connections with the ATL by placing retrograde tracer injections into the ATL: the temporal polar (n = 3), perirhinal (areas 35 and 36, n = 6), and inferotemporal cortices (area TE, n = 5), plus one additional deposit in the posterior parahippocampal cortex (area TF, n = 1). Anterograde tracer deposits into the dLPFC (A9 and A46, n = 2), the vLPFC (A46v, n = 2), and the orbitofrontal cortex (OF; n = 2) were placed for confirmation of those projections. The results showed that the vLPFC displays a moderate projection to rostral area TE and the dorsomedial portion of the temporal polar cortex; in contrast, the dLPFC connections with the ATL were weak. By comparison, the OFC and medial frontal cortices (MFC) showed dense connectivity with the ATL, namely, A13 with the temporopolar and perirhinal cortices. All areas of the MFC projected to the temporopolar cortex, albeit with a lower intensity. The functional significance of such paucity of LPFC afferents is unknown. J. Comp. Neurol. 523:2570–2598, 2015. © 2015 Wiley Periodicals, Inc.
Schematic representation of the dLPFC and vLPFC afferents to the ATL in Macaca fascicularis. Line thickness indicates the density of the projection. Whereas the vLPFC projects moderately to the rostral TE, the dLPFC presents sparse projections to the ATL. In contrast, the OFC and MFC display heavy projections. |
doi_str_mv | 10.1002/cne.23805 |
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The anatomical organization of the lateral prefrontal cortex (LPFC) afferents to the anterior part of the temporal lobe (ATL) remains to be clarified. The LPFC has two subdivisions, dorsal (dLPFC) and ventral (vLPFC), which have been linked to cognitive processes. The ATL includes several different cortical areas, namely, the temporal polar cortex and rostral parts of the perirhinal, inferotemporal, and anterior tip of the superior temporal gyrus cortices. Multiple sensory modalities converge in the ATL. All of them (except the rostral inferotemporal and superior temporal gyrus cortices) are components of the medial temporal lobe, which is critical for long‐term memory processing. We studied the LPFC connections with the ATL by placing retrograde tracer injections into the ATL: the temporal polar (n = 3), perirhinal (areas 35 and 36, n = 6), and inferotemporal cortices (area TE, n = 5), plus one additional deposit in the posterior parahippocampal cortex (area TF, n = 1). Anterograde tracer deposits into the dLPFC (A9 and A46, n = 2), the vLPFC (A46v, n = 2), and the orbitofrontal cortex (OF; n = 2) were placed for confirmation of those projections. The results showed that the vLPFC displays a moderate projection to rostral area TE and the dorsomedial portion of the temporal polar cortex; in contrast, the dLPFC connections with the ATL were weak. By comparison, the OFC and medial frontal cortices (MFC) showed dense connectivity with the ATL, namely, A13 with the temporopolar and perirhinal cortices. All areas of the MFC projected to the temporopolar cortex, albeit with a lower intensity. The functional significance of such paucity of LPFC afferents is unknown. J. Comp. Neurol. 523:2570–2598, 2015. © 2015 Wiley Periodicals, Inc.
Schematic representation of the dLPFC and vLPFC afferents to the ATL in Macaca fascicularis. Line thickness indicates the density of the projection. Whereas the vLPFC projects moderately to the rostral TE, the dLPFC presents sparse projections to the ATL. In contrast, the OFC and MFC display heavy projections.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.23805</identifier><identifier>PMID: 25975699</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Afferent Pathways - physiology ; afferents ; Amidines - metabolism ; Animals ; anterior temporal cortex ; Biotin - analogs & derivatives ; Biotin - metabolism ; Brain Mapping ; Dextrans - metabolism ; Fasting ; Macaca fascicularis ; Macaca fascicularis - anatomy & histology ; Male ; nonhuman primate ; prefrontal cortex ; Prefrontal Cortex - anatomy & histology ; Temporal Lobe - anatomy & histology ; Wheat Germ Agglutinin-Horseradish Peroxidase Conjugate - metabolism</subject><ispartof>Journal of comparative neurology (1911), 2015-12, Vol.523 (17), p.2570-2598</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5295-9392590ab4050a170a5fd318d3f9b424957306eef009f715162c71abf864f4773</citedby><cites>FETCH-LOGICAL-c5295-9392590ab4050a170a5fd318d3f9b424957306eef009f715162c71abf864f4773</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25975699$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mohedano-Moriano, Alicia</creatorcontrib><creatorcontrib>Muñoz-López, Mónica</creatorcontrib><creatorcontrib>Sanz-Arigita, Ernesto</creatorcontrib><creatorcontrib>Pró-Sistiaga, Palma</creatorcontrib><creatorcontrib>Martínez-Marcos, Alino</creatorcontrib><creatorcontrib>Legidos-Garcia, María Ester</creatorcontrib><creatorcontrib>Insausti, Ana María</creatorcontrib><creatorcontrib>Cebada-Sánchez, Sandra</creatorcontrib><creatorcontrib>Arroyo-Jiménez, María Del Mar</creatorcontrib><creatorcontrib>Marcos, Pilar</creatorcontrib><creatorcontrib>Artacho-Pérula, Emilio</creatorcontrib><creatorcontrib>Insausti, Ricardo</creatorcontrib><title>Prefrontal cortex afferents to the anterior temporal lobe in the Macaca fascicularis monkey</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>ABSTRACT
The anatomical organization of the lateral prefrontal cortex (LPFC) afferents to the anterior part of the temporal lobe (ATL) remains to be clarified. The LPFC has two subdivisions, dorsal (dLPFC) and ventral (vLPFC), which have been linked to cognitive processes. The ATL includes several different cortical areas, namely, the temporal polar cortex and rostral parts of the perirhinal, inferotemporal, and anterior tip of the superior temporal gyrus cortices. Multiple sensory modalities converge in the ATL. All of them (except the rostral inferotemporal and superior temporal gyrus cortices) are components of the medial temporal lobe, which is critical for long‐term memory processing. We studied the LPFC connections with the ATL by placing retrograde tracer injections into the ATL: the temporal polar (n = 3), perirhinal (areas 35 and 36, n = 6), and inferotemporal cortices (area TE, n = 5), plus one additional deposit in the posterior parahippocampal cortex (area TF, n = 1). Anterograde tracer deposits into the dLPFC (A9 and A46, n = 2), the vLPFC (A46v, n = 2), and the orbitofrontal cortex (OF; n = 2) were placed for confirmation of those projections. The results showed that the vLPFC displays a moderate projection to rostral area TE and the dorsomedial portion of the temporal polar cortex; in contrast, the dLPFC connections with the ATL were weak. By comparison, the OFC and medial frontal cortices (MFC) showed dense connectivity with the ATL, namely, A13 with the temporopolar and perirhinal cortices. All areas of the MFC projected to the temporopolar cortex, albeit with a lower intensity. The functional significance of such paucity of LPFC afferents is unknown. J. Comp. Neurol. 523:2570–2598, 2015. © 2015 Wiley Periodicals, Inc.
Schematic representation of the dLPFC and vLPFC afferents to the ATL in Macaca fascicularis. Line thickness indicates the density of the projection. Whereas the vLPFC projects moderately to the rostral TE, the dLPFC presents sparse projections to the ATL. In contrast, the OFC and MFC display heavy projections.</description><subject>Afferent Pathways - physiology</subject><subject>afferents</subject><subject>Amidines - metabolism</subject><subject>Animals</subject><subject>anterior temporal cortex</subject><subject>Biotin - analogs & derivatives</subject><subject>Biotin - metabolism</subject><subject>Brain Mapping</subject><subject>Dextrans - metabolism</subject><subject>Fasting</subject><subject>Macaca fascicularis</subject><subject>Macaca fascicularis - anatomy & histology</subject><subject>Male</subject><subject>nonhuman primate</subject><subject>prefrontal cortex</subject><subject>Prefrontal Cortex - anatomy & histology</subject><subject>Temporal Lobe - anatomy & histology</subject><subject>Wheat Germ Agglutinin-Horseradish Peroxidase Conjugate - metabolism</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkcFu1DAURS0EokNhwQ8gS2xgkdbPju14iaK2gEoBqYgFC8vxPIu0STy1E8H8PZ5O2wUSEvLCi3fe1bUPIS-BHQFj_NhPeMRFw-QjsgJmVGUaBY_JqsygMkbpA_Is5yvGmDGieUoOuDRaKmNW5MeXhCHFaXYD9THN-Ju6EDDhNGc6Rzr_ROqmGVMfE51x3MRUyCF2SPvpdvrJ-XJocNn3fhlc6jMd43SN2-fkSXBDxhd39yH5dnpy2b6vzj-ffWjfnVdeciMrI0zpw1xXM8kcaOZkWAto1iKYrua1kVowhRhK_aBBguJeg-tCo-pQay0OyZt97ibFmwXzbMc-exwGN2FcsgXNOTTQNPI_UGgMgNI79PVf6FVc0lQesqO0qaHULdTbPeVTzLn8pd2kfnRpa4HZnRxb5NhbOYV9dZe4dCOuH8h7GwU43gO_-gG3_06y7cXJfWS13-hzUfew4dK1VVpoab9fnNn2Y3vK2_rSfhV_AF7GpbA</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Mohedano-Moriano, Alicia</creator><creator>Muñoz-López, Mónica</creator><creator>Sanz-Arigita, Ernesto</creator><creator>Pró-Sistiaga, Palma</creator><creator>Martínez-Marcos, Alino</creator><creator>Legidos-Garcia, María Ester</creator><creator>Insausti, Ana María</creator><creator>Cebada-Sánchez, Sandra</creator><creator>Arroyo-Jiménez, María Del Mar</creator><creator>Marcos, Pilar</creator><creator>Artacho-Pérula, Emilio</creator><creator>Insausti, Ricardo</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20151201</creationdate><title>Prefrontal cortex afferents to the anterior temporal lobe in the Macaca fascicularis monkey</title><author>Mohedano-Moriano, Alicia ; Muñoz-López, Mónica ; Sanz-Arigita, Ernesto ; Pró-Sistiaga, Palma ; Martínez-Marcos, Alino ; Legidos-Garcia, María Ester ; Insausti, Ana María ; Cebada-Sánchez, Sandra ; Arroyo-Jiménez, María Del Mar ; Marcos, Pilar ; Artacho-Pérula, Emilio ; Insausti, Ricardo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5295-9392590ab4050a170a5fd318d3f9b424957306eef009f715162c71abf864f4773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Afferent Pathways - physiology</topic><topic>afferents</topic><topic>Amidines - metabolism</topic><topic>Animals</topic><topic>anterior temporal cortex</topic><topic>Biotin - analogs & derivatives</topic><topic>Biotin - metabolism</topic><topic>Brain Mapping</topic><topic>Dextrans - metabolism</topic><topic>Fasting</topic><topic>Macaca fascicularis</topic><topic>Macaca fascicularis - anatomy & histology</topic><topic>Male</topic><topic>nonhuman primate</topic><topic>prefrontal cortex</topic><topic>Prefrontal Cortex - anatomy & histology</topic><topic>Temporal Lobe - anatomy & histology</topic><topic>Wheat Germ Agglutinin-Horseradish Peroxidase Conjugate - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohedano-Moriano, Alicia</creatorcontrib><creatorcontrib>Muñoz-López, Mónica</creatorcontrib><creatorcontrib>Sanz-Arigita, Ernesto</creatorcontrib><creatorcontrib>Pró-Sistiaga, Palma</creatorcontrib><creatorcontrib>Martínez-Marcos, Alino</creatorcontrib><creatorcontrib>Legidos-Garcia, María Ester</creatorcontrib><creatorcontrib>Insausti, Ana María</creatorcontrib><creatorcontrib>Cebada-Sánchez, Sandra</creatorcontrib><creatorcontrib>Arroyo-Jiménez, María Del Mar</creatorcontrib><creatorcontrib>Marcos, Pilar</creatorcontrib><creatorcontrib>Artacho-Pérula, Emilio</creatorcontrib><creatorcontrib>Insausti, Ricardo</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mohedano-Moriano, Alicia</au><au>Muñoz-López, Mónica</au><au>Sanz-Arigita, Ernesto</au><au>Pró-Sistiaga, Palma</au><au>Martínez-Marcos, Alino</au><au>Legidos-Garcia, María Ester</au><au>Insausti, Ana María</au><au>Cebada-Sánchez, Sandra</au><au>Arroyo-Jiménez, María Del Mar</au><au>Marcos, Pilar</au><au>Artacho-Pérula, Emilio</au><au>Insausti, Ricardo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prefrontal cortex afferents to the anterior temporal lobe in the Macaca fascicularis monkey</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>523</volume><issue>17</issue><spage>2570</spage><epage>2598</epage><pages>2570-2598</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>ABSTRACT
The anatomical organization of the lateral prefrontal cortex (LPFC) afferents to the anterior part of the temporal lobe (ATL) remains to be clarified. The LPFC has two subdivisions, dorsal (dLPFC) and ventral (vLPFC), which have been linked to cognitive processes. The ATL includes several different cortical areas, namely, the temporal polar cortex and rostral parts of the perirhinal, inferotemporal, and anterior tip of the superior temporal gyrus cortices. Multiple sensory modalities converge in the ATL. All of them (except the rostral inferotemporal and superior temporal gyrus cortices) are components of the medial temporal lobe, which is critical for long‐term memory processing. We studied the LPFC connections with the ATL by placing retrograde tracer injections into the ATL: the temporal polar (n = 3), perirhinal (areas 35 and 36, n = 6), and inferotemporal cortices (area TE, n = 5), plus one additional deposit in the posterior parahippocampal cortex (area TF, n = 1). Anterograde tracer deposits into the dLPFC (A9 and A46, n = 2), the vLPFC (A46v, n = 2), and the orbitofrontal cortex (OF; n = 2) were placed for confirmation of those projections. The results showed that the vLPFC displays a moderate projection to rostral area TE and the dorsomedial portion of the temporal polar cortex; in contrast, the dLPFC connections with the ATL were weak. By comparison, the OFC and medial frontal cortices (MFC) showed dense connectivity with the ATL, namely, A13 with the temporopolar and perirhinal cortices. All areas of the MFC projected to the temporopolar cortex, albeit with a lower intensity. The functional significance of such paucity of LPFC afferents is unknown. J. Comp. Neurol. 523:2570–2598, 2015. © 2015 Wiley Periodicals, Inc.
Schematic representation of the dLPFC and vLPFC afferents to the ATL in Macaca fascicularis. Line thickness indicates the density of the projection. Whereas the vLPFC projects moderately to the rostral TE, the dLPFC presents sparse projections to the ATL. In contrast, the OFC and MFC display heavy projections.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25975699</pmid><doi>10.1002/cne.23805</doi><tpages>29</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Afferent Pathways - physiology afferents Amidines - metabolism Animals anterior temporal cortex Biotin - analogs & derivatives Biotin - metabolism Brain Mapping Dextrans - metabolism Fasting Macaca fascicularis Macaca fascicularis - anatomy & histology Male nonhuman primate prefrontal cortex Prefrontal Cortex - anatomy & histology Temporal Lobe - anatomy & histology Wheat Germ Agglutinin-Horseradish Peroxidase Conjugate - metabolism |
title | Prefrontal cortex afferents to the anterior temporal lobe in the Macaca fascicularis monkey |
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