Glunicate (LG 13979) protects the arterial wall from cholesterol-induced atherosclerotic changes in the rabbit without affecting plasma lipids
Glunicate is evaluated compared to nicotinic acid for effects on aortic atheromatous lesions, lipid parameters and factors involved in thrombosis and haemostasis in rabbits kept on a high-cholesterol diet for 12 weeks, using 2 doses of glunicate (0.17 and 0.69 g/day) and 1 of nicotinic acid (0.6 g/d...
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Veröffentlicht in: | Atherosclerosis 1984-01, Vol.53 (1), p.59-68 |
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description | Glunicate is evaluated compared to nicotinic acid for effects on aortic atheromatous lesions, lipid parameters and factors involved in thrombosis and haemostasis in rabbits kept on a high-cholesterol diet for 12 weeks, using 2 doses of glunicate (0.17 and 0.69 g/day) and 1 of nicotinic acid (0.6 g/day). Glunicate afforded dose-dependent protection of the arterial wall from atheromatous lesions and from cholesterol and collagen accumulation, while nicotinic acid hardly had any effect. These effects were completely independent of plasma lipid-lowering action, the plasma levels of all lipids being indistinguishable in all cholesterol-fed groups. In addition to inducing the expected changes in the lipid pattern, the atherogenic diet increased platelet aggregation in response to collagen but not to ADP, prolonged the APTT and lowered the plasma fibrinogen levels. Both glunicate and nicotinic acid counteracted the effects of the diet on platelet aggregation and on APTT, but only glunicate normalised the fibrinogen levels. There was no change in PT or in prostacyclin-like activity release from the mesenteric artery after the diet or diet plus drugs. |
doi_str_mv | 10.1016/0021-9150(84)90105-9 |
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Glunicate afforded dose-dependent protection of the arterial wall from atheromatous lesions and from cholesterol and collagen accumulation, while nicotinic acid hardly had any effect. These effects were completely independent of plasma lipid-lowering action, the plasma levels of all lipids being indistinguishable in all cholesterol-fed groups. In addition to inducing the expected changes in the lipid pattern, the atherogenic diet increased platelet aggregation in response to collagen but not to ADP, prolonged the APTT and lowered the plasma fibrinogen levels. Both glunicate and nicotinic acid counteracted the effects of the diet on platelet aggregation and on APTT, but only glunicate normalised the fibrinogen levels. There was no change in PT or in prostacyclin-like activity release from the mesenteric artery after the diet or diet plus drugs.</description><identifier>ISSN: 0021-9150</identifier><identifier>EISSN: 1879-1484</identifier><identifier>DOI: 10.1016/0021-9150(84)90105-9</identifier><identifier>PMID: 6238601</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ireland Ltd</publisher><subject>Animals ; Aorta ; Aorta - drug effects ; Arteriosclerosis - prevention & control ; Biological and medical sciences ; Blood Coagulation - drug effects ; Cholesterol fed rabbit ; Cholesterol, Dietary - administration & dosage ; Dose-Response Relationship, Drug ; Epoprostenol - metabolism ; General and cellular metabolism. Vitamins ; Glunicate (LG 13979) ; Haemostasis ; Hypercholesterolemia - complications ; Lipids - blood ; Medical sciences ; Niacin - pharmacology ; Niacinamide - analogs & derivatives ; Niacinamide - pharmacology ; Nicotinic acid ; Pharmacology. Drug treatments ; Plasma lipids ; Platelet aggregation ; Platelet Aggregation - drug effects ; Prostacyclin-like activity ; Rabbits</subject><ispartof>Atherosclerosis, 1984-01, Vol.53 (1), p.59-68</ispartof><rights>1984</rights><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-78d417248baab9d931c467ee38b3c64e2cb740734844d29f5c809320a3680ee83</citedby><cites>FETCH-LOGICAL-c481t-78d417248baab9d931c467ee38b3c64e2cb740734844d29f5c809320a3680ee83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0021-9150(84)90105-9$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9045903$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6238601$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Criscuoh, M.</creatorcontrib><creatorcontrib>Renzetti, A.R.</creatorcontrib><creatorcontrib>Subissi, A.</creatorcontrib><title>Glunicate (LG 13979) protects the arterial wall from cholesterol-induced atherosclerotic changes in the rabbit without affecting plasma lipids</title><title>Atherosclerosis</title><addtitle>Atherosclerosis</addtitle><description>Glunicate is evaluated compared to nicotinic acid for effects on aortic atheromatous lesions, lipid parameters and factors involved in thrombosis and haemostasis in rabbits kept on a high-cholesterol diet for 12 weeks, using 2 doses of glunicate (0.17 and 0.69 g/day) and 1 of nicotinic acid (0.6 g/day). Glunicate afforded dose-dependent protection of the arterial wall from atheromatous lesions and from cholesterol and collagen accumulation, while nicotinic acid hardly had any effect. These effects were completely independent of plasma lipid-lowering action, the plasma levels of all lipids being indistinguishable in all cholesterol-fed groups. In addition to inducing the expected changes in the lipid pattern, the atherogenic diet increased platelet aggregation in response to collagen but not to ADP, prolonged the APTT and lowered the plasma fibrinogen levels. Both glunicate and nicotinic acid counteracted the effects of the diet on platelet aggregation and on APTT, but only glunicate normalised the fibrinogen levels. There was no change in PT or in prostacyclin-like activity release from the mesenteric artery after the diet or diet plus drugs.</description><subject>Animals</subject><subject>Aorta</subject><subject>Aorta - drug effects</subject><subject>Arteriosclerosis - prevention & control</subject><subject>Biological and medical sciences</subject><subject>Blood Coagulation - drug effects</subject><subject>Cholesterol fed rabbit</subject><subject>Cholesterol, Dietary - administration & dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>Epoprostenol - metabolism</subject><subject>General and cellular metabolism. Vitamins</subject><subject>Glunicate (LG 13979)</subject><subject>Haemostasis</subject><subject>Hypercholesterolemia - complications</subject><subject>Lipids - blood</subject><subject>Medical sciences</subject><subject>Niacin - pharmacology</subject><subject>Niacinamide - analogs & derivatives</subject><subject>Niacinamide - pharmacology</subject><subject>Nicotinic acid</subject><subject>Pharmacology. Drug treatments</subject><subject>Plasma lipids</subject><subject>Platelet aggregation</subject><subject>Platelet Aggregation - drug effects</subject><subject>Prostacyclin-like activity</subject><subject>Rabbits</subject><issn>0021-9150</issn><issn>1879-1484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFu1DAQQC0EKtvCH4DkA0LtITCOvYl9qYQqWJBW4gJna-JMukZOsthOK36Cb8bbXe2Riy153sx43jD2RsAHAaL5CFCLyog1XGt1Y0DAujLP2Ero1lRCafWcrc7IS3aZ0i8AUK3QF-yiqaVuQKzY301YJu8wE7_ebriQpjU3fB_nTC4nnnfEMWaKHgN_xBD4EOeRu90cKJXnOVR-6hdHPcfCxjm5UM7sXWFwuqfE_fRUJWLX-cwffd7NS-Y4DKWBn-75PmAakQe_9316xV4MGBK9Pt1X7OeXzz_uvlbb75tvd5-2lVNa5KrVvRJtrXSH2JneSOFU0xJJ3UnXKKpd1ypoZbGg-toMa6fByBpQNhqItLxi7491y6S_lzKKHX1yFAJONC_JaiFlbXRTQHUEXZktRRrsPvoR4x8rwB7WYA-O7cGx1co-rcGakvb2VH_pRurPSSfvJf7uFMfkMAwRJ-fTGTOg1gZkwW6PGBUXD56iTc7TVHT7WPTZfvb__8c_rGikNg</recordid><startdate>19840101</startdate><enddate>19840101</enddate><creator>Criscuoh, M.</creator><creator>Renzetti, A.R.</creator><creator>Subissi, A.</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</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>19840101</creationdate><title>Glunicate (LG 13979) protects the arterial wall from cholesterol-induced atherosclerotic changes in the rabbit without affecting plasma lipids</title><author>Criscuoh, M. ; Renzetti, A.R. ; Subissi, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-78d417248baab9d931c467ee38b3c64e2cb740734844d29f5c809320a3680ee83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Animals</topic><topic>Aorta</topic><topic>Aorta - drug effects</topic><topic>Arteriosclerosis - prevention & control</topic><topic>Biological and medical sciences</topic><topic>Blood Coagulation - drug effects</topic><topic>Cholesterol fed rabbit</topic><topic>Cholesterol, Dietary - administration & dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>Epoprostenol - metabolism</topic><topic>General and cellular metabolism. Vitamins</topic><topic>Glunicate (LG 13979)</topic><topic>Haemostasis</topic><topic>Hypercholesterolemia - complications</topic><topic>Lipids - blood</topic><topic>Medical sciences</topic><topic>Niacin - pharmacology</topic><topic>Niacinamide - analogs & derivatives</topic><topic>Niacinamide - pharmacology</topic><topic>Nicotinic acid</topic><topic>Pharmacology. Drug treatments</topic><topic>Plasma lipids</topic><topic>Platelet aggregation</topic><topic>Platelet Aggregation - drug effects</topic><topic>Prostacyclin-like activity</topic><topic>Rabbits</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Criscuoh, M.</creatorcontrib><creatorcontrib>Renzetti, A.R.</creatorcontrib><creatorcontrib>Subissi, A.</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>Atherosclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Criscuoh, M.</au><au>Renzetti, A.R.</au><au>Subissi, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glunicate (LG 13979) protects the arterial wall from cholesterol-induced atherosclerotic changes in the rabbit without affecting plasma lipids</atitle><jtitle>Atherosclerosis</jtitle><addtitle>Atherosclerosis</addtitle><date>1984-01-01</date><risdate>1984</risdate><volume>53</volume><issue>1</issue><spage>59</spage><epage>68</epage><pages>59-68</pages><issn>0021-9150</issn><eissn>1879-1484</eissn><abstract>Glunicate is evaluated compared to nicotinic acid for effects on aortic atheromatous lesions, lipid parameters and factors involved in thrombosis and haemostasis in rabbits kept on a high-cholesterol diet for 12 weeks, using 2 doses of glunicate (0.17 and 0.69 g/day) and 1 of nicotinic acid (0.6 g/day). Glunicate afforded dose-dependent protection of the arterial wall from atheromatous lesions and from cholesterol and collagen accumulation, while nicotinic acid hardly had any effect. These effects were completely independent of plasma lipid-lowering action, the plasma levels of all lipids being indistinguishable in all cholesterol-fed groups. In addition to inducing the expected changes in the lipid pattern, the atherogenic diet increased platelet aggregation in response to collagen but not to ADP, prolonged the APTT and lowered the plasma fibrinogen levels. Both glunicate and nicotinic acid counteracted the effects of the diet on platelet aggregation and on APTT, but only glunicate normalised the fibrinogen levels. There was no change in PT or in prostacyclin-like activity release from the mesenteric artery after the diet or diet plus drugs.</abstract><cop>Amsterdam</cop><pub>Elsevier Ireland Ltd</pub><pmid>6238601</pmid><doi>10.1016/0021-9150(84)90105-9</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Aorta Aorta - drug effects Arteriosclerosis - prevention & control Biological and medical sciences Blood Coagulation - drug effects Cholesterol fed rabbit Cholesterol, Dietary - administration & dosage Dose-Response Relationship, Drug Epoprostenol - metabolism General and cellular metabolism. Vitamins Glunicate (LG 13979) Haemostasis Hypercholesterolemia - complications Lipids - blood Medical sciences Niacin - pharmacology Niacinamide - analogs & derivatives Niacinamide - pharmacology Nicotinic acid Pharmacology. Drug treatments Plasma lipids Platelet aggregation Platelet Aggregation - drug effects Prostacyclin-like activity Rabbits |
title | Glunicate (LG 13979) protects the arterial wall from cholesterol-induced atherosclerotic changes in the rabbit without affecting plasma lipids |
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