Integrated signaling in heterodimers and receptor mosaics of different types of GPCRs of the forebrain: relevance for schizophrenia
Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics...
Ausführliche Beschreibung
Autor*in: |
Fuxe, Kjell [verfasserIn] Marcellino, Daniel [verfasserIn] Woods, Amina S. [verfasserIn] Giuseppina, Leo [verfasserIn] Antonelli, Tiziana [verfasserIn] Ferraro, Luca [verfasserIn] Tanganelli, Sergio [verfasserIn] Agnati, Luigi F. [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2009 |
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Übergeordnetes Werk: |
Enthalten in: Journal of neural transmission - Wien [u.a.] : Springer, 1950, 116(2009), 8 vom: 21. Jan. |
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Übergeordnetes Werk: |
volume:116 ; year:2009 ; number:8 ; day:21 ; month:01 |
Links: |
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DOI / URN: |
10.1007/s00702-008-0174-9 |
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Katalog-ID: |
SPR00764406X |
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520 | |a Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics in the ventral striatum containing $ D_{2} $ receptors and 5-$ HT_{2A} $ receptors in cortical networks may contribute to disturbances of key pathways involving ventral striato-pallidal GABA neurons and mediodorsal thalamic prefrontal glutamate neurons that may lead to the development of schizophrenia. The ventral striatum transmits emotional information to the cerebral cortex through a $ D_{2} $ regulated accumbal–ventral pallidal–mediodorsal–prefrontal circuit which is of special interest to schizophrenia in view of the reduced number of glutamate mediodorsal–prefrontal projections associated with this disease. This circuit is especially vulnerable to $ D_{2} $ receptor activity in the nucleus accumbens, since it produces a reduction in the prefrontal glutamate drive from the mediodorsal nucleus. The following $ D_{2} $ receptor containing heterodimers/receptor mosaics are of special interest to schizophrenia: $ A_{2A} $–$ D_{2} $, mGluR5–$ D_{2} $, $ CB_{1} $–$ D_{2} $, $ NTS_{1} $–$ D_{2} $ and $ D_{2} $–$ D_{3} $ and are discussed in this review. They may have a differential distribution pattern in the local circuits of the ventral striato-pallidal GABA pathway, predominantly located extrasynaptically. Specifically, trimeric receptor mosaics consisting of $ A_{2A} $–$ D_{2} $–mGluR5 and $ CB_{1} $–$ D_{2} $–$ A_{2A} $ may also exist in these local circuits and are discussed. The integration of receptor signaling within assembled heterodimers/receptor mosaics is brought about by agonists and allosteric modulators. These cause the intramembrane receptor–receptor interactions, via allosteric mechanisms, to produce conformational changes that pass over the receptor interfaces. Exogenous and endogenous cooperativity is discussed as well as the role of the cortical mGluR2–5-$ HT_{2A} $ heterodimer/receptor mosaic in schizophrenia (Gonzalez-Maeso et al. 2008). Receptor–receptor interactions within receptor heterodimer/receptor mosaics of different receptors in the ventral striatum and cerebral cortex give novel strategies for treatment of schizophrenia involving, e.g., monotherapy with either $ A_{2A} $, mGluR5, $ CB_{1} $ or $ NTS_{1} $ agonists or combined therapies with some of these agonists combined with $ D_{2} $-like antagonists that specifically target the ventral striatum. In addition, a combined targeting of receptor mosaics in the ventral striatum and in the cerebral cortex should also be considered. | ||
700 | 1 | |a Marcellino, Daniel |e verfasserin |4 aut | |
700 | 1 | |a Woods, Amina S. |e verfasserin |4 aut | |
700 | 1 | |a Giuseppina, Leo |e verfasserin |4 aut | |
700 | 1 | |a Antonelli, Tiziana |e verfasserin |4 aut | |
700 | 1 | |a Ferraro, Luca |e verfasserin |4 aut | |
700 | 1 | |a Tanganelli, Sergio |e verfasserin |4 aut | |
700 | 1 | |a Agnati, Luigi F. |e verfasserin |4 aut | |
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10.1007/s00702-008-0174-9 doi (DE-627)SPR00764406X (SPR)s00702-008-0174-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Fuxe, Kjell verfasserin aut Integrated signaling in heterodimers and receptor mosaics of different types of GPCRs of the forebrain: relevance for schizophrenia 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics in the ventral striatum containing $ D_{2} $ receptors and 5-$ HT_{2A} $ receptors in cortical networks may contribute to disturbances of key pathways involving ventral striato-pallidal GABA neurons and mediodorsal thalamic prefrontal glutamate neurons that may lead to the development of schizophrenia. The ventral striatum transmits emotional information to the cerebral cortex through a $ D_{2} $ regulated accumbal–ventral pallidal–mediodorsal–prefrontal circuit which is of special interest to schizophrenia in view of the reduced number of glutamate mediodorsal–prefrontal projections associated with this disease. This circuit is especially vulnerable to $ D_{2} $ receptor activity in the nucleus accumbens, since it produces a reduction in the prefrontal glutamate drive from the mediodorsal nucleus. The following $ D_{2} $ receptor containing heterodimers/receptor mosaics are of special interest to schizophrenia: $ A_{2A} $–$ D_{2} $, mGluR5–$ D_{2} $, $ CB_{1} $–$ D_{2} $, $ NTS_{1} $–$ D_{2} $ and $ D_{2} $–$ D_{3} $ and are discussed in this review. They may have a differential distribution pattern in the local circuits of the ventral striato-pallidal GABA pathway, predominantly located extrasynaptically. Specifically, trimeric receptor mosaics consisting of $ A_{2A} $–$ D_{2} $–mGluR5 and $ CB_{1} $–$ D_{2} $–$ A_{2A} $ may also exist in these local circuits and are discussed. The integration of receptor signaling within assembled heterodimers/receptor mosaics is brought about by agonists and allosteric modulators. These cause the intramembrane receptor–receptor interactions, via allosteric mechanisms, to produce conformational changes that pass over the receptor interfaces. Exogenous and endogenous cooperativity is discussed as well as the role of the cortical mGluR2–5-$ HT_{2A} $ heterodimer/receptor mosaic in schizophrenia (Gonzalez-Maeso et al. 2008). Receptor–receptor interactions within receptor heterodimer/receptor mosaics of different receptors in the ventral striatum and cerebral cortex give novel strategies for treatment of schizophrenia involving, e.g., monotherapy with either $ A_{2A} $, mGluR5, $ CB_{1} $ or $ NTS_{1} $ agonists or combined therapies with some of these agonists combined with $ D_{2} $-like antagonists that specifically target the ventral striatum. In addition, a combined targeting of receptor mosaics in the ventral striatum and in the cerebral cortex should also be considered. Marcellino, Daniel verfasserin aut Woods, Amina S. verfasserin aut Giuseppina, Leo verfasserin aut Antonelli, Tiziana verfasserin aut Ferraro, Luca verfasserin aut Tanganelli, Sergio verfasserin aut Agnati, Luigi F. verfasserin aut Enthalten in Journal of neural transmission Wien [u.a.] : Springer, 1950 116(2009), 8 vom: 21. Jan. (DE-627)300185901 (DE-600)1481655-6 1435-1463 nnns volume:116 year:2009 number:8 day:21 month:01 https://dx.doi.org/10.1007/s00702-008-0174-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 116 2009 8 21 01 |
spelling |
10.1007/s00702-008-0174-9 doi (DE-627)SPR00764406X (SPR)s00702-008-0174-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Fuxe, Kjell verfasserin aut Integrated signaling in heterodimers and receptor mosaics of different types of GPCRs of the forebrain: relevance for schizophrenia 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics in the ventral striatum containing $ D_{2} $ receptors and 5-$ HT_{2A} $ receptors in cortical networks may contribute to disturbances of key pathways involving ventral striato-pallidal GABA neurons and mediodorsal thalamic prefrontal glutamate neurons that may lead to the development of schizophrenia. The ventral striatum transmits emotional information to the cerebral cortex through a $ D_{2} $ regulated accumbal–ventral pallidal–mediodorsal–prefrontal circuit which is of special interest to schizophrenia in view of the reduced number of glutamate mediodorsal–prefrontal projections associated with this disease. This circuit is especially vulnerable to $ D_{2} $ receptor activity in the nucleus accumbens, since it produces a reduction in the prefrontal glutamate drive from the mediodorsal nucleus. The following $ D_{2} $ receptor containing heterodimers/receptor mosaics are of special interest to schizophrenia: $ A_{2A} $–$ D_{2} $, mGluR5–$ D_{2} $, $ CB_{1} $–$ D_{2} $, $ NTS_{1} $–$ D_{2} $ and $ D_{2} $–$ D_{3} $ and are discussed in this review. They may have a differential distribution pattern in the local circuits of the ventral striato-pallidal GABA pathway, predominantly located extrasynaptically. Specifically, trimeric receptor mosaics consisting of $ A_{2A} $–$ D_{2} $–mGluR5 and $ CB_{1} $–$ D_{2} $–$ A_{2A} $ may also exist in these local circuits and are discussed. The integration of receptor signaling within assembled heterodimers/receptor mosaics is brought about by agonists and allosteric modulators. These cause the intramembrane receptor–receptor interactions, via allosteric mechanisms, to produce conformational changes that pass over the receptor interfaces. Exogenous and endogenous cooperativity is discussed as well as the role of the cortical mGluR2–5-$ HT_{2A} $ heterodimer/receptor mosaic in schizophrenia (Gonzalez-Maeso et al. 2008). Receptor–receptor interactions within receptor heterodimer/receptor mosaics of different receptors in the ventral striatum and cerebral cortex give novel strategies for treatment of schizophrenia involving, e.g., monotherapy with either $ A_{2A} $, mGluR5, $ CB_{1} $ or $ NTS_{1} $ agonists or combined therapies with some of these agonists combined with $ D_{2} $-like antagonists that specifically target the ventral striatum. In addition, a combined targeting of receptor mosaics in the ventral striatum and in the cerebral cortex should also be considered. Marcellino, Daniel verfasserin aut Woods, Amina S. verfasserin aut Giuseppina, Leo verfasserin aut Antonelli, Tiziana verfasserin aut Ferraro, Luca verfasserin aut Tanganelli, Sergio verfasserin aut Agnati, Luigi F. verfasserin aut Enthalten in Journal of neural transmission Wien [u.a.] : Springer, 1950 116(2009), 8 vom: 21. Jan. (DE-627)300185901 (DE-600)1481655-6 1435-1463 nnns volume:116 year:2009 number:8 day:21 month:01 https://dx.doi.org/10.1007/s00702-008-0174-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 116 2009 8 21 01 |
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10.1007/s00702-008-0174-9 doi (DE-627)SPR00764406X (SPR)s00702-008-0174-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Fuxe, Kjell verfasserin aut Integrated signaling in heterodimers and receptor mosaics of different types of GPCRs of the forebrain: relevance for schizophrenia 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics in the ventral striatum containing $ D_{2} $ receptors and 5-$ HT_{2A} $ receptors in cortical networks may contribute to disturbances of key pathways involving ventral striato-pallidal GABA neurons and mediodorsal thalamic prefrontal glutamate neurons that may lead to the development of schizophrenia. The ventral striatum transmits emotional information to the cerebral cortex through a $ D_{2} $ regulated accumbal–ventral pallidal–mediodorsal–prefrontal circuit which is of special interest to schizophrenia in view of the reduced number of glutamate mediodorsal–prefrontal projections associated with this disease. This circuit is especially vulnerable to $ D_{2} $ receptor activity in the nucleus accumbens, since it produces a reduction in the prefrontal glutamate drive from the mediodorsal nucleus. The following $ D_{2} $ receptor containing heterodimers/receptor mosaics are of special interest to schizophrenia: $ A_{2A} $–$ D_{2} $, mGluR5–$ D_{2} $, $ CB_{1} $–$ D_{2} $, $ NTS_{1} $–$ D_{2} $ and $ D_{2} $–$ D_{3} $ and are discussed in this review. They may have a differential distribution pattern in the local circuits of the ventral striato-pallidal GABA pathway, predominantly located extrasynaptically. Specifically, trimeric receptor mosaics consisting of $ A_{2A} $–$ D_{2} $–mGluR5 and $ CB_{1} $–$ D_{2} $–$ A_{2A} $ may also exist in these local circuits and are discussed. The integration of receptor signaling within assembled heterodimers/receptor mosaics is brought about by agonists and allosteric modulators. These cause the intramembrane receptor–receptor interactions, via allosteric mechanisms, to produce conformational changes that pass over the receptor interfaces. Exogenous and endogenous cooperativity is discussed as well as the role of the cortical mGluR2–5-$ HT_{2A} $ heterodimer/receptor mosaic in schizophrenia (Gonzalez-Maeso et al. 2008). Receptor–receptor interactions within receptor heterodimer/receptor mosaics of different receptors in the ventral striatum and cerebral cortex give novel strategies for treatment of schizophrenia involving, e.g., monotherapy with either $ A_{2A} $, mGluR5, $ CB_{1} $ or $ NTS_{1} $ agonists or combined therapies with some of these agonists combined with $ D_{2} $-like antagonists that specifically target the ventral striatum. In addition, a combined targeting of receptor mosaics in the ventral striatum and in the cerebral cortex should also be considered. Marcellino, Daniel verfasserin aut Woods, Amina S. verfasserin aut Giuseppina, Leo verfasserin aut Antonelli, Tiziana verfasserin aut Ferraro, Luca verfasserin aut Tanganelli, Sergio verfasserin aut Agnati, Luigi F. verfasserin aut Enthalten in Journal of neural transmission Wien [u.a.] : Springer, 1950 116(2009), 8 vom: 21. Jan. (DE-627)300185901 (DE-600)1481655-6 1435-1463 nnns volume:116 year:2009 number:8 day:21 month:01 https://dx.doi.org/10.1007/s00702-008-0174-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 116 2009 8 21 01 |
allfieldsGer |
10.1007/s00702-008-0174-9 doi (DE-627)SPR00764406X (SPR)s00702-008-0174-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Fuxe, Kjell verfasserin aut Integrated signaling in heterodimers and receptor mosaics of different types of GPCRs of the forebrain: relevance for schizophrenia 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics in the ventral striatum containing $ D_{2} $ receptors and 5-$ HT_{2A} $ receptors in cortical networks may contribute to disturbances of key pathways involving ventral striato-pallidal GABA neurons and mediodorsal thalamic prefrontal glutamate neurons that may lead to the development of schizophrenia. The ventral striatum transmits emotional information to the cerebral cortex through a $ D_{2} $ regulated accumbal–ventral pallidal–mediodorsal–prefrontal circuit which is of special interest to schizophrenia in view of the reduced number of glutamate mediodorsal–prefrontal projections associated with this disease. This circuit is especially vulnerable to $ D_{2} $ receptor activity in the nucleus accumbens, since it produces a reduction in the prefrontal glutamate drive from the mediodorsal nucleus. The following $ D_{2} $ receptor containing heterodimers/receptor mosaics are of special interest to schizophrenia: $ A_{2A} $–$ D_{2} $, mGluR5–$ D_{2} $, $ CB_{1} $–$ D_{2} $, $ NTS_{1} $–$ D_{2} $ and $ D_{2} $–$ D_{3} $ and are discussed in this review. They may have a differential distribution pattern in the local circuits of the ventral striato-pallidal GABA pathway, predominantly located extrasynaptically. Specifically, trimeric receptor mosaics consisting of $ A_{2A} $–$ D_{2} $–mGluR5 and $ CB_{1} $–$ D_{2} $–$ A_{2A} $ may also exist in these local circuits and are discussed. The integration of receptor signaling within assembled heterodimers/receptor mosaics is brought about by agonists and allosteric modulators. These cause the intramembrane receptor–receptor interactions, via allosteric mechanisms, to produce conformational changes that pass over the receptor interfaces. Exogenous and endogenous cooperativity is discussed as well as the role of the cortical mGluR2–5-$ HT_{2A} $ heterodimer/receptor mosaic in schizophrenia (Gonzalez-Maeso et al. 2008). Receptor–receptor interactions within receptor heterodimer/receptor mosaics of different receptors in the ventral striatum and cerebral cortex give novel strategies for treatment of schizophrenia involving, e.g., monotherapy with either $ A_{2A} $, mGluR5, $ CB_{1} $ or $ NTS_{1} $ agonists or combined therapies with some of these agonists combined with $ D_{2} $-like antagonists that specifically target the ventral striatum. In addition, a combined targeting of receptor mosaics in the ventral striatum and in the cerebral cortex should also be considered. Marcellino, Daniel verfasserin aut Woods, Amina S. verfasserin aut Giuseppina, Leo verfasserin aut Antonelli, Tiziana verfasserin aut Ferraro, Luca verfasserin aut Tanganelli, Sergio verfasserin aut Agnati, Luigi F. verfasserin aut Enthalten in Journal of neural transmission Wien [u.a.] : Springer, 1950 116(2009), 8 vom: 21. Jan. (DE-627)300185901 (DE-600)1481655-6 1435-1463 nnns volume:116 year:2009 number:8 day:21 month:01 https://dx.doi.org/10.1007/s00702-008-0174-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 116 2009 8 21 01 |
allfieldsSound |
10.1007/s00702-008-0174-9 doi (DE-627)SPR00764406X (SPR)s00702-008-0174-9-e DE-627 ger DE-627 rakwb eng 610 ASE 44.90 bkl Fuxe, Kjell verfasserin aut Integrated signaling in heterodimers and receptor mosaics of different types of GPCRs of the forebrain: relevance for schizophrenia 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics in the ventral striatum containing $ D_{2} $ receptors and 5-$ HT_{2A} $ receptors in cortical networks may contribute to disturbances of key pathways involving ventral striato-pallidal GABA neurons and mediodorsal thalamic prefrontal glutamate neurons that may lead to the development of schizophrenia. The ventral striatum transmits emotional information to the cerebral cortex through a $ D_{2} $ regulated accumbal–ventral pallidal–mediodorsal–prefrontal circuit which is of special interest to schizophrenia in view of the reduced number of glutamate mediodorsal–prefrontal projections associated with this disease. This circuit is especially vulnerable to $ D_{2} $ receptor activity in the nucleus accumbens, since it produces a reduction in the prefrontal glutamate drive from the mediodorsal nucleus. The following $ D_{2} $ receptor containing heterodimers/receptor mosaics are of special interest to schizophrenia: $ A_{2A} $–$ D_{2} $, mGluR5–$ D_{2} $, $ CB_{1} $–$ D_{2} $, $ NTS_{1} $–$ D_{2} $ and $ D_{2} $–$ D_{3} $ and are discussed in this review. They may have a differential distribution pattern in the local circuits of the ventral striato-pallidal GABA pathway, predominantly located extrasynaptically. Specifically, trimeric receptor mosaics consisting of $ A_{2A} $–$ D_{2} $–mGluR5 and $ CB_{1} $–$ D_{2} $–$ A_{2A} $ may also exist in these local circuits and are discussed. The integration of receptor signaling within assembled heterodimers/receptor mosaics is brought about by agonists and allosteric modulators. These cause the intramembrane receptor–receptor interactions, via allosteric mechanisms, to produce conformational changes that pass over the receptor interfaces. Exogenous and endogenous cooperativity is discussed as well as the role of the cortical mGluR2–5-$ HT_{2A} $ heterodimer/receptor mosaic in schizophrenia (Gonzalez-Maeso et al. 2008). Receptor–receptor interactions within receptor heterodimer/receptor mosaics of different receptors in the ventral striatum and cerebral cortex give novel strategies for treatment of schizophrenia involving, e.g., monotherapy with either $ A_{2A} $, mGluR5, $ CB_{1} $ or $ NTS_{1} $ agonists or combined therapies with some of these agonists combined with $ D_{2} $-like antagonists that specifically target the ventral striatum. In addition, a combined targeting of receptor mosaics in the ventral striatum and in the cerebral cortex should also be considered. Marcellino, Daniel verfasserin aut Woods, Amina S. verfasserin aut Giuseppina, Leo verfasserin aut Antonelli, Tiziana verfasserin aut Ferraro, Luca verfasserin aut Tanganelli, Sergio verfasserin aut Agnati, Luigi F. verfasserin aut Enthalten in Journal of neural transmission Wien [u.a.] : Springer, 1950 116(2009), 8 vom: 21. Jan. (DE-627)300185901 (DE-600)1481655-6 1435-1463 nnns volume:116 year:2009 number:8 day:21 month:01 https://dx.doi.org/10.1007/s00702-008-0174-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 44.90 ASE AR 116 2009 8 21 01 |
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Fuxe, Kjell @@aut@@ Marcellino, Daniel @@aut@@ Woods, Amina S. @@aut@@ Giuseppina, Leo @@aut@@ Antonelli, Tiziana @@aut@@ Ferraro, Luca @@aut@@ Tanganelli, Sergio @@aut@@ Agnati, Luigi F. @@aut@@ |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR00764406X</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519215439.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201005s2009 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s00702-008-0174-9</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR00764406X</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s00702-008-0174-9-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">ASE</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">44.90</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Fuxe, Kjell</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Integrated signaling in heterodimers and receptor mosaics of different types of GPCRs of the forebrain: relevance for schizophrenia</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2009</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics in the ventral striatum containing $ D_{2} $ receptors and 5-$ HT_{2A} $ receptors in cortical networks may contribute to disturbances of key pathways involving ventral striato-pallidal GABA neurons and mediodorsal thalamic prefrontal glutamate neurons that may lead to the development of schizophrenia. The ventral striatum transmits emotional information to the cerebral cortex through a $ D_{2} $ regulated accumbal–ventral pallidal–mediodorsal–prefrontal circuit which is of special interest to schizophrenia in view of the reduced number of glutamate mediodorsal–prefrontal projections associated with this disease. This circuit is especially vulnerable to $ D_{2} $ receptor activity in the nucleus accumbens, since it produces a reduction in the prefrontal glutamate drive from the mediodorsal nucleus. The following $ D_{2} $ receptor containing heterodimers/receptor mosaics are of special interest to schizophrenia: $ A_{2A} $–$ D_{2} $, mGluR5–$ D_{2} $, $ CB_{1} $–$ D_{2} $, $ NTS_{1} $–$ D_{2} $ and $ D_{2} $–$ D_{3} $ and are discussed in this review. They may have a differential distribution pattern in the local circuits of the ventral striato-pallidal GABA pathway, predominantly located extrasynaptically. Specifically, trimeric receptor mosaics consisting of $ A_{2A} $–$ D_{2} $–mGluR5 and $ CB_{1} $–$ D_{2} $–$ A_{2A} $ may also exist in these local circuits and are discussed. The integration of receptor signaling within assembled heterodimers/receptor mosaics is brought about by agonists and allosteric modulators. These cause the intramembrane receptor–receptor interactions, via allosteric mechanisms, to produce conformational changes that pass over the receptor interfaces. Exogenous and endogenous cooperativity is discussed as well as the role of the cortical mGluR2–5-$ HT_{2A} $ heterodimer/receptor mosaic in schizophrenia (Gonzalez-Maeso et al. 2008). Receptor–receptor interactions within receptor heterodimer/receptor mosaics of different receptors in the ventral striatum and cerebral cortex give novel strategies for treatment of schizophrenia involving, e.g., monotherapy with either $ A_{2A} $, mGluR5, $ CB_{1} $ or $ NTS_{1} $ agonists or combined therapies with some of these agonists combined with $ D_{2} $-like antagonists that specifically target the ventral striatum. In addition, a combined targeting of receptor mosaics in the ventral striatum and in the cerebral cortex should also be considered.</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Marcellino, Daniel</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Woods, Amina S.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Giuseppina, Leo</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Antonelli, Tiziana</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ferraro, Luca</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Tanganelli, Sergio</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Agnati, Luigi F.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of neural transmission</subfield><subfield code="d">Wien [u.a.] : Springer, 1950</subfield><subfield code="g">116(2009), 8 vom: 21. 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Fuxe, Kjell |
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610 ASE 44.90 bkl Integrated signaling in heterodimers and receptor mosaics of different types of GPCRs of the forebrain: relevance for schizophrenia |
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verfasserin |
title_sort |
integrated signaling in heterodimers and receptor mosaics of different types of gpcrs of the forebrain: relevance for schizophrenia |
title_auth |
Integrated signaling in heterodimers and receptor mosaics of different types of GPCRs of the forebrain: relevance for schizophrenia |
abstract |
Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics in the ventral striatum containing $ D_{2} $ receptors and 5-$ HT_{2A} $ receptors in cortical networks may contribute to disturbances of key pathways involving ventral striato-pallidal GABA neurons and mediodorsal thalamic prefrontal glutamate neurons that may lead to the development of schizophrenia. The ventral striatum transmits emotional information to the cerebral cortex through a $ D_{2} $ regulated accumbal–ventral pallidal–mediodorsal–prefrontal circuit which is of special interest to schizophrenia in view of the reduced number of glutamate mediodorsal–prefrontal projections associated with this disease. This circuit is especially vulnerable to $ D_{2} $ receptor activity in the nucleus accumbens, since it produces a reduction in the prefrontal glutamate drive from the mediodorsal nucleus. The following $ D_{2} $ receptor containing heterodimers/receptor mosaics are of special interest to schizophrenia: $ A_{2A} $–$ D_{2} $, mGluR5–$ D_{2} $, $ CB_{1} $–$ D_{2} $, $ NTS_{1} $–$ D_{2} $ and $ D_{2} $–$ D_{3} $ and are discussed in this review. They may have a differential distribution pattern in the local circuits of the ventral striato-pallidal GABA pathway, predominantly located extrasynaptically. Specifically, trimeric receptor mosaics consisting of $ A_{2A} $–$ D_{2} $–mGluR5 and $ CB_{1} $–$ D_{2} $–$ A_{2A} $ may also exist in these local circuits and are discussed. The integration of receptor signaling within assembled heterodimers/receptor mosaics is brought about by agonists and allosteric modulators. These cause the intramembrane receptor–receptor interactions, via allosteric mechanisms, to produce conformational changes that pass over the receptor interfaces. Exogenous and endogenous cooperativity is discussed as well as the role of the cortical mGluR2–5-$ HT_{2A} $ heterodimer/receptor mosaic in schizophrenia (Gonzalez-Maeso et al. 2008). Receptor–receptor interactions within receptor heterodimer/receptor mosaics of different receptors in the ventral striatum and cerebral cortex give novel strategies for treatment of schizophrenia involving, e.g., monotherapy with either $ A_{2A} $, mGluR5, $ CB_{1} $ or $ NTS_{1} $ agonists or combined therapies with some of these agonists combined with $ D_{2} $-like antagonists that specifically target the ventral striatum. In addition, a combined targeting of receptor mosaics in the ventral striatum and in the cerebral cortex should also be considered. |
abstractGer |
Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics in the ventral striatum containing $ D_{2} $ receptors and 5-$ HT_{2A} $ receptors in cortical networks may contribute to disturbances of key pathways involving ventral striato-pallidal GABA neurons and mediodorsal thalamic prefrontal glutamate neurons that may lead to the development of schizophrenia. The ventral striatum transmits emotional information to the cerebral cortex through a $ D_{2} $ regulated accumbal–ventral pallidal–mediodorsal–prefrontal circuit which is of special interest to schizophrenia in view of the reduced number of glutamate mediodorsal–prefrontal projections associated with this disease. This circuit is especially vulnerable to $ D_{2} $ receptor activity in the nucleus accumbens, since it produces a reduction in the prefrontal glutamate drive from the mediodorsal nucleus. The following $ D_{2} $ receptor containing heterodimers/receptor mosaics are of special interest to schizophrenia: $ A_{2A} $–$ D_{2} $, mGluR5–$ D_{2} $, $ CB_{1} $–$ D_{2} $, $ NTS_{1} $–$ D_{2} $ and $ D_{2} $–$ D_{3} $ and are discussed in this review. They may have a differential distribution pattern in the local circuits of the ventral striato-pallidal GABA pathway, predominantly located extrasynaptically. Specifically, trimeric receptor mosaics consisting of $ A_{2A} $–$ D_{2} $–mGluR5 and $ CB_{1} $–$ D_{2} $–$ A_{2A} $ may also exist in these local circuits and are discussed. The integration of receptor signaling within assembled heterodimers/receptor mosaics is brought about by agonists and allosteric modulators. These cause the intramembrane receptor–receptor interactions, via allosteric mechanisms, to produce conformational changes that pass over the receptor interfaces. Exogenous and endogenous cooperativity is discussed as well as the role of the cortical mGluR2–5-$ HT_{2A} $ heterodimer/receptor mosaic in schizophrenia (Gonzalez-Maeso et al. 2008). Receptor–receptor interactions within receptor heterodimer/receptor mosaics of different receptors in the ventral striatum and cerebral cortex give novel strategies for treatment of schizophrenia involving, e.g., monotherapy with either $ A_{2A} $, mGluR5, $ CB_{1} $ or $ NTS_{1} $ agonists or combined therapies with some of these agonists combined with $ D_{2} $-like antagonists that specifically target the ventral striatum. In addition, a combined targeting of receptor mosaics in the ventral striatum and in the cerebral cortex should also be considered. |
abstract_unstemmed |
Abstract Receptor–receptor interactions within receptor heterodimers and receptor mosaics formed by different types of GPCRs represent an important integrative mechanism for signaling in brain networks at the level of the plasma membrane. The malfunction of special heterodimers and receptor mosaics in the ventral striatum containing $ D_{2} $ receptors and 5-$ HT_{2A} $ receptors in cortical networks may contribute to disturbances of key pathways involving ventral striato-pallidal GABA neurons and mediodorsal thalamic prefrontal glutamate neurons that may lead to the development of schizophrenia. The ventral striatum transmits emotional information to the cerebral cortex through a $ D_{2} $ regulated accumbal–ventral pallidal–mediodorsal–prefrontal circuit which is of special interest to schizophrenia in view of the reduced number of glutamate mediodorsal–prefrontal projections associated with this disease. This circuit is especially vulnerable to $ D_{2} $ receptor activity in the nucleus accumbens, since it produces a reduction in the prefrontal glutamate drive from the mediodorsal nucleus. The following $ D_{2} $ receptor containing heterodimers/receptor mosaics are of special interest to schizophrenia: $ A_{2A} $–$ D_{2} $, mGluR5–$ D_{2} $, $ CB_{1} $–$ D_{2} $, $ NTS_{1} $–$ D_{2} $ and $ D_{2} $–$ D_{3} $ and are discussed in this review. They may have a differential distribution pattern in the local circuits of the ventral striato-pallidal GABA pathway, predominantly located extrasynaptically. Specifically, trimeric receptor mosaics consisting of $ A_{2A} $–$ D_{2} $–mGluR5 and $ CB_{1} $–$ D_{2} $–$ A_{2A} $ may also exist in these local circuits and are discussed. The integration of receptor signaling within assembled heterodimers/receptor mosaics is brought about by agonists and allosteric modulators. These cause the intramembrane receptor–receptor interactions, via allosteric mechanisms, to produce conformational changes that pass over the receptor interfaces. Exogenous and endogenous cooperativity is discussed as well as the role of the cortical mGluR2–5-$ HT_{2A} $ heterodimer/receptor mosaic in schizophrenia (Gonzalez-Maeso et al. 2008). Receptor–receptor interactions within receptor heterodimer/receptor mosaics of different receptors in the ventral striatum and cerebral cortex give novel strategies for treatment of schizophrenia involving, e.g., monotherapy with either $ A_{2A} $, mGluR5, $ CB_{1} $ or $ NTS_{1} $ agonists or combined therapies with some of these agonists combined with $ D_{2} $-like antagonists that specifically target the ventral striatum. In addition, a combined targeting of receptor mosaics in the ventral striatum and in the cerebral cortex should also be considered. |
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container_issue |
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title_short |
Integrated signaling in heterodimers and receptor mosaics of different types of GPCRs of the forebrain: relevance for schizophrenia |
url |
https://dx.doi.org/10.1007/s00702-008-0174-9 |
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Marcellino, Daniel Woods, Amina S. Giuseppina, Leo Antonelli, Tiziana Ferraro, Luca Tanganelli, Sergio Agnati, Luigi F. |
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Marcellino, Daniel Woods, Amina S. Giuseppina, Leo Antonelli, Tiziana Ferraro, Luca Tanganelli, Sergio Agnati, Luigi F. |
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up_date |
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score |
7.3995953 |