Increased psychological responses and divergent neuroendocrine responses to m-CPP and ipsapirone in patients with panic disorder
In patients with panic disorder and /or agoraphobia (PDA) an increased sensitivity of central 5-HT2C receptors and a decreased responsiveness of 5-HT1A receptors has been postulated. In the present study, neuroendocrine challenges were performed using oral doses of the non-selective 5-HT2C agonist m...
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Veröffentlicht in: | International clinical psychopharmacology 2000-05, Vol.15 (3), p.153-161 |
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description | In patients with panic disorder and /or agoraphobia (PDA) an increased sensitivity of central 5-HT2C receptors and a decreased responsiveness of 5-HT1A receptors has been postulated. In the present study, neuroendocrine challenges were performed using oral doses of the non-selective 5-HT2C agonist m-chlorophenylpiperazine (m-CPP) (0.4 mg/kg), the selective 5-HT1A antagonist ipsapirone (0.3 mg/kg), and placebo in 40 patients with PDA and 12 healthy controls in order to compare 5-HT2C and 5-HT1A-specific psychobehavioural and neuroendocrine response patterns. At baseline, all psychobehavioural variables and the plasma concentration of noradrenaline (NE) were significantly increased in the patient group compared to the controls. The administration of m-CPP or ipsapirone was followed by comparable psychological symptoms and, in 55% of all patients, panic attacks. In comparison to the control subjects, patients were characterized by significantly higher psychological reactions to both challenge agents and a significantly higher NE response to m-CPP. In the patient group, there was also a trend towards an increased cortisol response after administration of m-CPP and a decreased cortisol and hypothermia response after administration of ipsapirone compared to the control group. The neuroendocrine findings of our study support earlier reports of opposite changes in the responsiveness of 5-HT2C and 5-HT1A-related receptors in PDA patients. The behavioural hypersensitivity to both, m-CPP and ipsapiron, shows that the provocation of anxiety and other psychological symptoms might be influenced by |
doi_str_mv | 10.1097/00004850-200015030-00004 |
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In the present study, neuroendocrine challenges were performed using oral doses of the non-selective 5-HT2C agonist m-chlorophenylpiperazine (m-CPP) (0.4 mg/kg), the selective 5-HT1A antagonist ipsapirone (0.3 mg/kg), and placebo in 40 patients with PDA and 12 healthy controls in order to compare 5-HT2C and 5-HT1A-specific psychobehavioural and neuroendocrine response patterns. At baseline, all psychobehavioural variables and the plasma concentration of noradrenaline (NE) were significantly increased in the patient group compared to the controls. The administration of m-CPP or ipsapirone was followed by comparable psychological symptoms and, in 55% of all patients, panic attacks. In comparison to the control subjects, patients were characterized by significantly higher psychological reactions to both challenge agents and a significantly higher NE response to m-CPP. In the patient group, there was also a trend towards an increased cortisol response after administration of m-CPP and a decreased cortisol and hypothermia response after administration of ipsapirone compared to the control group. The neuroendocrine findings of our study support earlier reports of opposite changes in the responsiveness of 5-HT2C and 5-HT1A-related receptors in PDA patients. The behavioural hypersensitivity to both, m-CPP and ipsapiron, shows that the provocation of anxiety and other psychological symptoms might be influenced by</description><identifier>ISSN: 0268-1315</identifier><identifier>EISSN: 1473-5857</identifier><identifier>DOI: 10.1097/00004850-200015030-00004</identifier><identifier>PMID: 10870873</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins, Inc</publisher><subject>Adolescent ; Adult ; Adult and adolescent clinical studies ; Anxiety disorders. Neuroses ; Biological and medical sciences ; Female ; Humans ; Hydrocortisone - blood ; Hypothermia, Induced ; Male ; Medical sciences ; Neuropharmacology ; Neurotransmitters. Neurotransmission. Receptors ; Panic disorder ; Panic Disorder - physiopathology ; Pharmacology. Drug treatments ; Piperazines - pharmacology ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Pyrimidines - pharmacology ; Receptors, Serotonin - physiology ; Serotonin Receptor Agonists - pharmacology ; Serotoninergic system</subject><ispartof>International clinical psychopharmacology, 2000-05, Vol.15 (3), p.153-161</ispartof><rights>2000 Lippincott Williams & Wilkins, Inc.</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3854-c95dbff4ab0487c1f36dcc7ed51ad0371bcb729aba65c68ccde01ec3913b512e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1361360$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10870873$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Broocks, A</creatorcontrib><creatorcontrib>Bandelow, B</creatorcontrib><creatorcontrib>George, A</creatorcontrib><creatorcontrib>Jestrabeck, C</creatorcontrib><creatorcontrib>Opitz, M</creatorcontrib><creatorcontrib>Bartmann, U</creatorcontrib><creatorcontrib>Gleiter, C H</creatorcontrib><creatorcontrib>Meineke, I</creatorcontrib><creatorcontrib>Roed, I.-S</creatorcontrib><creatorcontrib>Rüther, E</creatorcontrib><creatorcontrib>Hajak, G</creatorcontrib><title>Increased psychological responses and divergent neuroendocrine responses to m-CPP and ipsapirone in patients with panic disorder</title><title>International clinical psychopharmacology</title><addtitle>Int Clin Psychopharmacol</addtitle><description>In patients with panic disorder and /or agoraphobia (PDA) an increased sensitivity of central 5-HT2C receptors and a decreased responsiveness of 5-HT1A receptors has been postulated. In the present study, neuroendocrine challenges were performed using oral doses of the non-selective 5-HT2C agonist m-chlorophenylpiperazine (m-CPP) (0.4 mg/kg), the selective 5-HT1A antagonist ipsapirone (0.3 mg/kg), and placebo in 40 patients with PDA and 12 healthy controls in order to compare 5-HT2C and 5-HT1A-specific psychobehavioural and neuroendocrine response patterns. At baseline, all psychobehavioural variables and the plasma concentration of noradrenaline (NE) were significantly increased in the patient group compared to the controls. The administration of m-CPP or ipsapirone was followed by comparable psychological symptoms and, in 55% of all patients, panic attacks. In comparison to the control subjects, patients were characterized by significantly higher psychological reactions to both challenge agents and a significantly higher NE response to m-CPP. In the patient group, there was also a trend towards an increased cortisol response after administration of m-CPP and a decreased cortisol and hypothermia response after administration of ipsapirone compared to the control group. The neuroendocrine findings of our study support earlier reports of opposite changes in the responsiveness of 5-HT2C and 5-HT1A-related receptors in PDA patients. The behavioural hypersensitivity to both, m-CPP and ipsapiron, shows that the provocation of anxiety and other psychological symptoms might be influenced by</description><subject>Adolescent</subject><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Anxiety disorders. Neuroses</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Humans</subject><subject>Hydrocortisone - blood</subject><subject>Hypothermia, Induced</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neuropharmacology</subject><subject>Neurotransmitters. Neurotransmission. Receptors</subject><subject>Panic disorder</subject><subject>Panic Disorder - physiopathology</subject><subject>Pharmacology. Drug treatments</subject><subject>Piperazines - pharmacology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Pyrimidines - pharmacology</subject><subject>Receptors, Serotonin - physiology</subject><subject>Serotonin Receptor Agonists - pharmacology</subject><subject>Serotoninergic system</subject><issn>0268-1315</issn><issn>1473-5857</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kcFu1DAQhi0EotvCKyAfELcUO47j5IhWlFaqRA_0HDnjSdeQtYMnYdUbj47bbKEXrJE8M_r-sfwPY1yKcyla81HkUzVaFGVOpBZKFI-tF2wjK6MK3Wjzkm1EWTeFVFKfsFOi70KUQrbVa3YiRWNyqA37fRUgoSV0fKJ72MUx3nmwI09IUwyExG1w3PlfmO4wzDzgkiIGFyH5gM-wOfJ9sb25eeT9RHbyKWbCBz7Z2Wct8YOfd7kKHvJEislhesNeDXYkfHu8z9jtxedv28vi-uuXq-2n6wJUo6sCWu36Yahsnz9uQA6qdgAGnZbWCWVkD70pW9vbWkPdADgUEkG1UvValqjO2Id17pTizwVp7vaeAMfRBowLdUaWUmjTZLBZQUiRKOHQTcnvbbrvpOge3O-e3O_-ur-2svTd8Y2l36N7JlztzsD7I2ApmzwkG8DTP07VOUTGqhU7xHHGRD_G5YCp26Ed5133v-WrP2hcn5c</recordid><startdate>200005</startdate><enddate>200005</enddate><creator>Broocks, A</creator><creator>Bandelow, B</creator><creator>George, A</creator><creator>Jestrabeck, C</creator><creator>Opitz, M</creator><creator>Bartmann, U</creator><creator>Gleiter, C H</creator><creator>Meineke, I</creator><creator>Roed, I.-S</creator><creator>Rüther, E</creator><creator>Hajak, G</creator><general>Lippincott Williams & Wilkins, Inc</general><general>Lippincott Williams & Wilkins</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>200005</creationdate><title>Increased psychological responses and divergent neuroendocrine responses to m-CPP and ipsapirone in patients with panic disorder</title><author>Broocks, A ; Bandelow, B ; George, A ; Jestrabeck, C ; Opitz, M ; Bartmann, U ; Gleiter, C H ; Meineke, I ; Roed, I.-S ; Rüther, E ; Hajak, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3854-c95dbff4ab0487c1f36dcc7ed51ad0371bcb729aba65c68ccde01ec3913b512e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Anxiety disorders. Neuroses</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Humans</topic><topic>Hydrocortisone - blood</topic><topic>Hypothermia, Induced</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neuropharmacology</topic><topic>Neurotransmitters. Neurotransmission. Receptors</topic><topic>Panic disorder</topic><topic>Panic Disorder - physiopathology</topic><topic>Pharmacology. Drug treatments</topic><topic>Piperazines - pharmacology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Pyrimidines - pharmacology</topic><topic>Receptors, Serotonin - physiology</topic><topic>Serotonin Receptor Agonists - pharmacology</topic><topic>Serotoninergic system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Broocks, A</creatorcontrib><creatorcontrib>Bandelow, B</creatorcontrib><creatorcontrib>George, A</creatorcontrib><creatorcontrib>Jestrabeck, C</creatorcontrib><creatorcontrib>Opitz, M</creatorcontrib><creatorcontrib>Bartmann, U</creatorcontrib><creatorcontrib>Gleiter, C H</creatorcontrib><creatorcontrib>Meineke, I</creatorcontrib><creatorcontrib>Roed, I.-S</creatorcontrib><creatorcontrib>Rüther, E</creatorcontrib><creatorcontrib>Hajak, G</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International clinical psychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Broocks, A</au><au>Bandelow, B</au><au>George, A</au><au>Jestrabeck, C</au><au>Opitz, M</au><au>Bartmann, U</au><au>Gleiter, C H</au><au>Meineke, I</au><au>Roed, I.-S</au><au>Rüther, E</au><au>Hajak, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased psychological responses and divergent neuroendocrine responses to m-CPP and ipsapirone in patients with panic disorder</atitle><jtitle>International clinical psychopharmacology</jtitle><addtitle>Int Clin Psychopharmacol</addtitle><date>2000-05</date><risdate>2000</risdate><volume>15</volume><issue>3</issue><spage>153</spage><epage>161</epage><pages>153-161</pages><issn>0268-1315</issn><eissn>1473-5857</eissn><abstract>In patients with panic disorder and /or agoraphobia (PDA) an increased sensitivity of central 5-HT2C receptors and a decreased responsiveness of 5-HT1A receptors has been postulated. In the present study, neuroendocrine challenges were performed using oral doses of the non-selective 5-HT2C agonist m-chlorophenylpiperazine (m-CPP) (0.4 mg/kg), the selective 5-HT1A antagonist ipsapirone (0.3 mg/kg), and placebo in 40 patients with PDA and 12 healthy controls in order to compare 5-HT2C and 5-HT1A-specific psychobehavioural and neuroendocrine response patterns. At baseline, all psychobehavioural variables and the plasma concentration of noradrenaline (NE) were significantly increased in the patient group compared to the controls. The administration of m-CPP or ipsapirone was followed by comparable psychological symptoms and, in 55% of all patients, panic attacks. In comparison to the control subjects, patients were characterized by significantly higher psychological reactions to both challenge agents and a significantly higher NE response to m-CPP. In the patient group, there was also a trend towards an increased cortisol response after administration of m-CPP and a decreased cortisol and hypothermia response after administration of ipsapirone compared to the control group. The neuroendocrine findings of our study support earlier reports of opposite changes in the responsiveness of 5-HT2C and 5-HT1A-related receptors in PDA patients. The behavioural hypersensitivity to both, m-CPP and ipsapiron, shows that the provocation of anxiety and other psychological symptoms might be influenced by</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>10870873</pmid><doi>10.1097/00004850-200015030-00004</doi><tpages>9</tpages></addata></record> |
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subjects | Adolescent Adult Adult and adolescent clinical studies Anxiety disorders. Neuroses Biological and medical sciences Female Humans Hydrocortisone - blood Hypothermia, Induced Male Medical sciences Neuropharmacology Neurotransmitters. Neurotransmission. Receptors Panic disorder Panic Disorder - physiopathology Pharmacology. Drug treatments Piperazines - pharmacology Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Pyrimidines - pharmacology Receptors, Serotonin - physiology Serotonin Receptor Agonists - pharmacology Serotoninergic system |
title | Increased psychological responses and divergent neuroendocrine responses to m-CPP and ipsapirone in patients with panic disorder |
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