Effects of Pyrazinoylguanidine on the Glucose-Fatty Acid Cycle in Normal Subjects and Patients with Non-Insulin-Dependent Diabetes Mellitus
Pyrazinoylguanidine (PZG) reduced the hyperglycemia, hyperinsulinemia, and hyperlipidemia of patients with non‐insulin‐dependent diabetes mellitus (NIDDM) as well as of normal subjects receiving hydrochlorothiazide (HCTZ). Mechanisms are proposed by which PZG downregulated the elevated glucose‐fatty...
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Veröffentlicht in: | Journal of clinical pharmacology 1993-09, Vol.33 (9), p.823-831 |
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creator | Vesell, Elliot S. Chambers, Charles E. Passananti, G. Thomas Demers, Laurence M. Beyer Jr, Karl H. |
description | Pyrazinoylguanidine (PZG) reduced the hyperglycemia, hyperinsulinemia, and hyperlipidemia of patients with non‐insulin‐dependent diabetes mellitus (NIDDM) as well as of normal subjects receiving hydrochlorothiazide (HCTZ). Mechanisms are proposed by which PZG downregulated the elevated glucose‐fatty acid cycle toward a more normal level in NIDDM patients and in non‐diabetic subjects maintained on HCTZ. Despite maintenance of these NIDDM patients on their current antihypertensive medication, PZG reduced further their systolic and diastolic pressures. PZG was well tolerated by both normal and NIDDM patients. |
doi_str_mv | 10.1002/j.1552-4604.1993.tb01958.x |
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Thomas</creatorcontrib><creatorcontrib>Demers, Laurence M.</creatorcontrib><creatorcontrib>Beyer Jr, Karl H.</creatorcontrib><title>Effects of Pyrazinoylguanidine on the Glucose-Fatty Acid Cycle in Normal Subjects and Patients with Non-Insulin-Dependent Diabetes Mellitus</title><title>Journal of clinical pharmacology</title><addtitle>J Clin Pharmacol</addtitle><description>Pyrazinoylguanidine (PZG) reduced the hyperglycemia, hyperinsulinemia, and hyperlipidemia of patients with non‐insulin‐dependent diabetes mellitus (NIDDM) as well as of normal subjects receiving hydrochlorothiazide (HCTZ). Mechanisms are proposed by which PZG downregulated the elevated glucose‐fatty acid cycle toward a more normal level in NIDDM patients and in non‐diabetic subjects maintained on HCTZ. Despite maintenance of these NIDDM patients on their current antihypertensive medication, PZG reduced further their systolic and diastolic pressures. PZG was well tolerated by both normal and NIDDM patients.</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - metabolism</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Down-Regulation</subject><subject>Fatty Acids - metabolism</subject><subject>Female</subject><subject>General and cellular metabolism. Vitamins</subject><subject>Glucose Tolerance Test</subject><subject>Guanidines - pharmacology</subject><subject>Humans</subject><subject>Hydrochlorothiazide - pharmacology</subject><subject>Insulin - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Pyrazines - pharmacology</subject><subject>Uremia - drug therapy</subject><issn>0091-2700</issn><issn>1552-4604</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUd1u0zAYjRBolMEjIFkIcZdgO3Zic8XUbe2mMYr4vbMc5wtzlzoldrSGV-ClcWjVe6782ed8x0fnJMkrgjOCMX27zgjnNGUFZhmRMs9ChYnkIts9SmZH6HEyw1iSlJYYP02eeb_GmBSMk5PkRFBaslLOkj8XTQMmeNQ1aDX2-rd13dj-HLSztXWAOofCHaBFO5jOQ3qpQxjRmbE1mo-mBWQduu36jW7R56Fa_1PSrkYrHSy4eHmw4S4yXHrl_NBal57DFlwdMXRudQUBPPoAbWvD4J8nTxrdenhxOE-Tr5cXX-bL9Obj4mp-dpMalguR6pJLwMAMphXXhAAVsqx5Fd8wJxUrtBYNE1rEScpamLLSkubAcywZZSw_Td7sdbd992sAH9TGehNNaAfd4FVZYC44FZH4bk80fed9D43a9naj-1ERrKYm1FpNcaspbjU1oQ5NqF1cfnn4Zag2UB9XD9FH_PUB197otum1M9YfaUySQpaTh_d72oNtYfwPA-p6vlpOY5RI9xLWB9gdJXR_r4oyL7n6frtQP66_fYq2lirP_wICtLaQ</recordid><startdate>199309</startdate><enddate>199309</enddate><creator>Vesell, Elliot S.</creator><creator>Chambers, Charles E.</creator><creator>Passananti, G. Thomas</creator><creator>Demers, Laurence M.</creator><creator>Beyer Jr, Karl H.</creator><general>Blackwell Publishing Ltd</general><general>Sage Science</general><scope>BSCLL</scope><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>199309</creationdate><title>Effects of Pyrazinoylguanidine on the Glucose-Fatty Acid Cycle in Normal Subjects and Patients with Non-Insulin-Dependent Diabetes Mellitus</title><author>Vesell, Elliot S. ; Chambers, Charles E. ; Passananti, G. Thomas ; Demers, Laurence M. ; Beyer Jr, Karl H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4388-a759e0e4c02b5a11e2897d5be0e051b46aa8f48a846a99d8c7ba923e530942443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - metabolism</topic><topic>Diabetes Mellitus, Type 2 - metabolism</topic><topic>Down-Regulation</topic><topic>Fatty Acids - metabolism</topic><topic>Female</topic><topic>General and cellular metabolism. Vitamins</topic><topic>Glucose Tolerance Test</topic><topic>Guanidines - pharmacology</topic><topic>Humans</topic><topic>Hydrochlorothiazide - pharmacology</topic><topic>Insulin - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Pyrazines - pharmacology</topic><topic>Uremia - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vesell, Elliot S.</creatorcontrib><creatorcontrib>Chambers, Charles E.</creatorcontrib><creatorcontrib>Passananti, G. 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Thomas</au><au>Demers, Laurence M.</au><au>Beyer Jr, Karl H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Pyrazinoylguanidine on the Glucose-Fatty Acid Cycle in Normal Subjects and Patients with Non-Insulin-Dependent Diabetes Mellitus</atitle><jtitle>Journal of clinical pharmacology</jtitle><addtitle>J Clin Pharmacol</addtitle><date>1993-09</date><risdate>1993</risdate><volume>33</volume><issue>9</issue><spage>823</spage><epage>831</epage><pages>823-831</pages><issn>0091-2700</issn><eissn>1552-4604</eissn><coden>JCPCBR</coden><abstract>Pyrazinoylguanidine (PZG) reduced the hyperglycemia, hyperinsulinemia, and hyperlipidemia of patients with non‐insulin‐dependent diabetes mellitus (NIDDM) as well as of normal subjects receiving hydrochlorothiazide (HCTZ). Mechanisms are proposed by which PZG downregulated the elevated glucose‐fatty acid cycle toward a more normal level in NIDDM patients and in non‐diabetic subjects maintained on HCTZ. Despite maintenance of these NIDDM patients on their current antihypertensive medication, PZG reduced further their systolic and diastolic pressures. PZG was well tolerated by both normal and NIDDM patients.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>8227479</pmid><doi>10.1002/j.1552-4604.1993.tb01958.x</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged Biological and medical sciences Blood Glucose - metabolism Diabetes Mellitus, Type 2 - metabolism Down-Regulation Fatty Acids - metabolism Female General and cellular metabolism. Vitamins Glucose Tolerance Test Guanidines - pharmacology Humans Hydrochlorothiazide - pharmacology Insulin - blood Male Medical sciences Middle Aged Pharmacology. Drug treatments Pyrazines - pharmacology Uremia - drug therapy |
title | Effects of Pyrazinoylguanidine on the Glucose-Fatty Acid Cycle in Normal Subjects and Patients with Non-Insulin-Dependent Diabetes Mellitus |
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