Protection of pancreatic beta-cell by the potential antioxidant bis-o-hydroxycinnamoyl methane, analogue of natural curcuminoid in experimental diabetes
To evaluate the antioxidant defense by bis-o-hydroxycinnamoylmethane, analogue of the naturally occurring curcuminoid bis-demethoxycurcumin in streptozotocin induced diabetes in male Wistar rats and its possible protection of pancreatic beta-cell against gradual loss under diabetic condition. Male w...
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Veröffentlicht in: | Journal of pharmacy & pharmaceutical sciences 2003-09, Vol.6 (3), p.327 |
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description | To evaluate the antioxidant defense by bis-o-hydroxycinnamoylmethane, analogue of the naturally occurring curcuminoid bis-demethoxycurcumin in streptozotocin induced diabetes in male Wistar rats and its possible protection of pancreatic beta-cell against gradual loss under diabetic condition.
Male wistar rats were divided into five groups. Group1 served as control rats. Group2 was control rats treated intragastrically with bis-o-hydroxycinnamoyl methane at a dose of 15 mg/kg body weight for 45 days. Group3, 4 and 5 rats were injected with 40 mg /kg body weight of streptozotocin to induce diabetes. Group4 rats were treated with the drug similar to group2 and group5 rats treated with the reference drug glibenclamide intragastrically for a similar period. After 45 days, the levels of plasma glucose, glycated hemoglobin, enzymic antioxidants (SOD, CAT) and non-enzymic antioxidants Vit C, Vit E was determined. Histopathological sections of the pancreas were examined.
The levels of plasma glucose and glycated hemoglobin which were elevated in group3 diabetic rats were reduced after treatment with the drug. The antioxidant levels showed an increase in the case of treated diabetic rats as compared to group3 diabetic rats. The islets were shrunken in group3 diabetic rats in comparison to normal rats. In the treated diabetic rats there was expansion of islets.
The experimental drug bis-o-hydroxycinnamoylmethane enhances the antioxidant defense against reactive oxygen species produced under hyperglycemic conditions and thus protects the pancreatic b -cell against loss and exhibits antidiabetic property. |
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Male wistar rats were divided into five groups. Group1 served as control rats. Group2 was control rats treated intragastrically with bis-o-hydroxycinnamoyl methane at a dose of 15 mg/kg body weight for 45 days. Group3, 4 and 5 rats were injected with 40 mg /kg body weight of streptozotocin to induce diabetes. Group4 rats were treated with the drug similar to group2 and group5 rats treated with the reference drug glibenclamide intragastrically for a similar period. After 45 days, the levels of plasma glucose, glycated hemoglobin, enzymic antioxidants (SOD, CAT) and non-enzymic antioxidants Vit C, Vit E was determined. Histopathological sections of the pancreas were examined.
The levels of plasma glucose and glycated hemoglobin which were elevated in group3 diabetic rats were reduced after treatment with the drug. The antioxidant levels showed an increase in the case of treated diabetic rats as compared to group3 diabetic rats. The islets were shrunken in group3 diabetic rats in comparison to normal rats. In the treated diabetic rats there was expansion of islets.
The experimental drug bis-o-hydroxycinnamoylmethane enhances the antioxidant defense against reactive oxygen species produced under hyperglycemic conditions and thus protects the pancreatic b -cell against loss and exhibits antidiabetic property.</description><identifier>EISSN: 1482-1826</identifier><identifier>PMID: 14738713</identifier><language>eng</language><publisher>Canada</publisher><subject>Animals ; Antioxidants - pharmacology ; Blood Glucose - metabolism ; Catalase - metabolism ; Curcumin - analogs & derivatives ; Curcumin - pharmacology ; Diabetes Mellitus, Experimental - chemically induced ; Diabetes Mellitus, Experimental - metabolism ; Diabetes Mellitus, Experimental - pathology ; Diarylheptanoids ; Islets of Langerhans - drug effects ; Islets of Langerhans - metabolism ; Male ; Rats ; Rats, Wistar ; Reactive Oxygen Species - metabolism ; Streptozocin ; Superoxide Dismutase - metabolism</subject><ispartof>Journal of pharmacy & pharmaceutical sciences, 2003-09, Vol.6 (3), p.327</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14738713$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Srivivasan, Anusuya</creatorcontrib><creatorcontrib>Menon, Venugopal P</creatorcontrib><creatorcontrib>Periaswamy, Viswanathan</creatorcontrib><creatorcontrib>Rajasekaran, K N</creatorcontrib><title>Protection of pancreatic beta-cell by the potential antioxidant bis-o-hydroxycinnamoyl methane, analogue of natural curcuminoid in experimental diabetes</title><title>Journal of pharmacy & pharmaceutical sciences</title><addtitle>J Pharm Pharm Sci</addtitle><description>To evaluate the antioxidant defense by bis-o-hydroxycinnamoylmethane, analogue of the naturally occurring curcuminoid bis-demethoxycurcumin in streptozotocin induced diabetes in male Wistar rats and its possible protection of pancreatic beta-cell against gradual loss under diabetic condition.
Male wistar rats were divided into five groups. Group1 served as control rats. Group2 was control rats treated intragastrically with bis-o-hydroxycinnamoyl methane at a dose of 15 mg/kg body weight for 45 days. Group3, 4 and 5 rats were injected with 40 mg /kg body weight of streptozotocin to induce diabetes. Group4 rats were treated with the drug similar to group2 and group5 rats treated with the reference drug glibenclamide intragastrically for a similar period. After 45 days, the levels of plasma glucose, glycated hemoglobin, enzymic antioxidants (SOD, CAT) and non-enzymic antioxidants Vit C, Vit E was determined. Histopathological sections of the pancreas were examined.
The levels of plasma glucose and glycated hemoglobin which were elevated in group3 diabetic rats were reduced after treatment with the drug. The antioxidant levels showed an increase in the case of treated diabetic rats as compared to group3 diabetic rats. The islets were shrunken in group3 diabetic rats in comparison to normal rats. In the treated diabetic rats there was expansion of islets.
The experimental drug bis-o-hydroxycinnamoylmethane enhances the antioxidant defense against reactive oxygen species produced under hyperglycemic conditions and thus protects the pancreatic b -cell against loss and exhibits antidiabetic property.</description><subject>Animals</subject><subject>Antioxidants - pharmacology</subject><subject>Blood Glucose - metabolism</subject><subject>Catalase - metabolism</subject><subject>Curcumin - analogs & derivatives</subject><subject>Curcumin - pharmacology</subject><subject>Diabetes Mellitus, Experimental - chemically induced</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Diabetes Mellitus, Experimental - pathology</subject><subject>Diarylheptanoids</subject><subject>Islets of Langerhans - drug effects</subject><subject>Islets of Langerhans - metabolism</subject><subject>Male</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Streptozocin</subject><subject>Superoxide Dismutase - metabolism</subject><issn>1482-1826</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kNtKxDAQhosg7rr6CpIHMNAc2mYvZfEEC3qh18tkMnUjbVLaFLZv4uMaUa--i_nnm-E_K9ZCG8mFkfWquJymz7KUSm7Li2IldKNMI9S6-HodYyJMPgYWWzZAwJEgeWSWEnCkrmN2YelIbMjBkDx0DDLiybtMZv3EIz8uboynBX0I0MelYz2lIwS6zVno4sdMP_YAaR7zPs4jzr0P0TvmA6PTQKPvszzPnId8maar4ryFbqLrP26K94f7t90T3788Pu_u9nwQUiZOaEyJorKiRkQLjWpridrYVjcSUAkNpHW9rZTA0rVaaF3lVkxdCXCqbtWmuPn1DrPtyR2G_AmMy-G_IvUNVoZmHw</recordid><startdate>200309</startdate><enddate>200309</enddate><creator>Srivivasan, Anusuya</creator><creator>Menon, Venugopal P</creator><creator>Periaswamy, Viswanathan</creator><creator>Rajasekaran, K N</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>200309</creationdate><title>Protection of pancreatic beta-cell by the potential antioxidant bis-o-hydroxycinnamoyl methane, analogue of natural curcuminoid in experimental diabetes</title><author>Srivivasan, Anusuya ; Menon, Venugopal P ; Periaswamy, Viswanathan ; Rajasekaran, K N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p122t-ec880c15b16cccba73f62c48bf472ac314ae4469531c0df414454828651ad36f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Antioxidants - pharmacology</topic><topic>Blood Glucose - metabolism</topic><topic>Catalase - metabolism</topic><topic>Curcumin - analogs & derivatives</topic><topic>Curcumin - pharmacology</topic><topic>Diabetes Mellitus, Experimental - chemically induced</topic><topic>Diabetes Mellitus, Experimental - metabolism</topic><topic>Diabetes Mellitus, Experimental - pathology</topic><topic>Diarylheptanoids</topic><topic>Islets of Langerhans - drug effects</topic><topic>Islets of Langerhans - metabolism</topic><topic>Male</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Streptozocin</topic><topic>Superoxide Dismutase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Srivivasan, Anusuya</creatorcontrib><creatorcontrib>Menon, Venugopal P</creatorcontrib><creatorcontrib>Periaswamy, Viswanathan</creatorcontrib><creatorcontrib>Rajasekaran, K N</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Journal of pharmacy & pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Srivivasan, Anusuya</au><au>Menon, Venugopal P</au><au>Periaswamy, Viswanathan</au><au>Rajasekaran, K N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protection of pancreatic beta-cell by the potential antioxidant bis-o-hydroxycinnamoyl methane, analogue of natural curcuminoid in experimental diabetes</atitle><jtitle>Journal of pharmacy & pharmaceutical sciences</jtitle><addtitle>J Pharm Pharm Sci</addtitle><date>2003-09</date><risdate>2003</risdate><volume>6</volume><issue>3</issue><spage>327</spage><pages>327-</pages><eissn>1482-1826</eissn><abstract>To evaluate the antioxidant defense by bis-o-hydroxycinnamoylmethane, analogue of the naturally occurring curcuminoid bis-demethoxycurcumin in streptozotocin induced diabetes in male Wistar rats and its possible protection of pancreatic beta-cell against gradual loss under diabetic condition.
Male wistar rats were divided into five groups. Group1 served as control rats. Group2 was control rats treated intragastrically with bis-o-hydroxycinnamoyl methane at a dose of 15 mg/kg body weight for 45 days. Group3, 4 and 5 rats were injected with 40 mg /kg body weight of streptozotocin to induce diabetes. Group4 rats were treated with the drug similar to group2 and group5 rats treated with the reference drug glibenclamide intragastrically for a similar period. After 45 days, the levels of plasma glucose, glycated hemoglobin, enzymic antioxidants (SOD, CAT) and non-enzymic antioxidants Vit C, Vit E was determined. Histopathological sections of the pancreas were examined.
The levels of plasma glucose and glycated hemoglobin which were elevated in group3 diabetic rats were reduced after treatment with the drug. The antioxidant levels showed an increase in the case of treated diabetic rats as compared to group3 diabetic rats. The islets were shrunken in group3 diabetic rats in comparison to normal rats. In the treated diabetic rats there was expansion of islets.
The experimental drug bis-o-hydroxycinnamoylmethane enhances the antioxidant defense against reactive oxygen species produced under hyperglycemic conditions and thus protects the pancreatic b -cell against loss and exhibits antidiabetic property.</abstract><cop>Canada</cop><pmid>14738713</pmid></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Free Full-Text Journals in Chemistry |
subjects | Animals Antioxidants - pharmacology Blood Glucose - metabolism Catalase - metabolism Curcumin - analogs & derivatives Curcumin - pharmacology Diabetes Mellitus, Experimental - chemically induced Diabetes Mellitus, Experimental - metabolism Diabetes Mellitus, Experimental - pathology Diarylheptanoids Islets of Langerhans - drug effects Islets of Langerhans - metabolism Male Rats Rats, Wistar Reactive Oxygen Species - metabolism Streptozocin Superoxide Dismutase - metabolism |
title | Protection of pancreatic beta-cell by the potential antioxidant bis-o-hydroxycinnamoyl methane, analogue of natural curcuminoid in experimental diabetes |
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