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Effects of thalidomide and 3-phthalimido-3-(3,4-dimethoxyphenyl)-propanamide on bile duct obstruction-induced cirrhosis in the rat
Tumor necrosis factor‐alpha (TNF‐α) plays a central role in cellular necrosis, apoptosis, organ failure, tissue damage, inflammation, and fibrosis. These processes, occurring in liver injury, may lead to cirrhosis. Thalidomide and its analogs have shown to be effective TNF‐α inhibitors. The aim of t...
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Published in: | Drug development research 2001-12, Vol.54 (4), p.209-218 |
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description | Tumor necrosis factor‐alpha (TNF‐α) plays a central role in cellular necrosis, apoptosis, organ failure, tissue damage, inflammation, and fibrosis. These processes, occurring in liver injury, may lead to cirrhosis. Thalidomide and its analogs have shown to be effective TNF‐α inhibitors. The aim of this work was to synthesize a thalidomide analog, the 3‐phthalimido‐3‐(3,4‐dimethoxyphenyl)‐propanamide (PDP) and to evaluate its hepatoprotective properties on bile duct obstruction‐induced cirrhosis. Synthesis, purification, and spectroscopic characterization of PDP were carried out. Thalidomide (200 mg/kg) or PDP (15 mg/kg) were administered to sham (Sh) or bile duct ligated (BDL) rats. The animals were sacrificed 28 days after treatments. Alkaline phosphatase (Alk. Phosph.), γ‐glutamyl transpeptidase (γ‐GTP) and alanine aminotransferase (ALT) enzyme activities, bilirubins, and TNF‐α concentrations were evaluated in plasma. Collagen was estimated by the liver hydroxyproline content and histopathology was performed. Both drugs showed partial amelioration of cirrhosis. However, the hepatoprotective effects of thalidomide were poor when compared to those afforded by PDP. While PDP improved the majority of the biochemical markers of liver injury and prevented partial but significantly collagen accumulation, thalidomide showed only modest beneficial effects on bilirubins and ALT. PDP was effective in preventing the increase in plasma TNF‐α levels, while thalidomide not only failed to inhibit TNF‐α, but increased it. Differences between thalidomide and PDP effectiveness may be due to their stability and different mechanism of action, as reported by others. Inhibition of proinflamatory cytokines is an interesting pharmacological aim to treat cirrhosis. Drug Dev. Res. 54:209–218, 2001. © 2002 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/ddr.10022 |
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These processes, occurring in liver injury, may lead to cirrhosis. Thalidomide and its analogs have shown to be effective TNF‐α inhibitors. The aim of this work was to synthesize a thalidomide analog, the 3‐phthalimido‐3‐(3,4‐dimethoxyphenyl)‐propanamide (PDP) and to evaluate its hepatoprotective properties on bile duct obstruction‐induced cirrhosis. Synthesis, purification, and spectroscopic characterization of PDP were carried out. Thalidomide (200 mg/kg) or PDP (15 mg/kg) were administered to sham (Sh) or bile duct ligated (BDL) rats. The animals were sacrificed 28 days after treatments. Alkaline phosphatase (Alk. Phosph.), γ‐glutamyl transpeptidase (γ‐GTP) and alanine aminotransferase (ALT) enzyme activities, bilirubins, and TNF‐α concentrations were evaluated in plasma. Collagen was estimated by the liver hydroxyproline content and histopathology was performed. Both drugs showed partial amelioration of cirrhosis. However, the hepatoprotective effects of thalidomide were poor when compared to those afforded by PDP. While PDP improved the majority of the biochemical markers of liver injury and prevented partial but significantly collagen accumulation, thalidomide showed only modest beneficial effects on bilirubins and ALT. PDP was effective in preventing the increase in plasma TNF‐α levels, while thalidomide not only failed to inhibit TNF‐α, but increased it. Differences between thalidomide and PDP effectiveness may be due to their stability and different mechanism of action, as reported by others. Inhibition of proinflamatory cytokines is an interesting pharmacological aim to treat cirrhosis. Drug Dev. Res. 54:209–218, 2001. © 2002 Wiley‐Liss, Inc.</description><identifier>ISSN: 0272-4391</identifier><identifier>EISSN: 1098-2299</identifier><identifier>DOI: 10.1002/ddr.10022</identifier><identifier>CODEN: DDREDK</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; cirrhosis ; citokines ; Digestive system ; liver ; Medical sciences ; Pharmacology. 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Res</addtitle><description>Tumor necrosis factor‐alpha (TNF‐α) plays a central role in cellular necrosis, apoptosis, organ failure, tissue damage, inflammation, and fibrosis. These processes, occurring in liver injury, may lead to cirrhosis. Thalidomide and its analogs have shown to be effective TNF‐α inhibitors. The aim of this work was to synthesize a thalidomide analog, the 3‐phthalimido‐3‐(3,4‐dimethoxyphenyl)‐propanamide (PDP) and to evaluate its hepatoprotective properties on bile duct obstruction‐induced cirrhosis. Synthesis, purification, and spectroscopic characterization of PDP were carried out. Thalidomide (200 mg/kg) or PDP (15 mg/kg) were administered to sham (Sh) or bile duct ligated (BDL) rats. The animals were sacrificed 28 days after treatments. Alkaline phosphatase (Alk. Phosph.), γ‐glutamyl transpeptidase (γ‐GTP) and alanine aminotransferase (ALT) enzyme activities, bilirubins, and TNF‐α concentrations were evaluated in plasma. Collagen was estimated by the liver hydroxyproline content and histopathology was performed. Both drugs showed partial amelioration of cirrhosis. However, the hepatoprotective effects of thalidomide were poor when compared to those afforded by PDP. While PDP improved the majority of the biochemical markers of liver injury and prevented partial but significantly collagen accumulation, thalidomide showed only modest beneficial effects on bilirubins and ALT. PDP was effective in preventing the increase in plasma TNF‐α levels, while thalidomide not only failed to inhibit TNF‐α, but increased it. Differences between thalidomide and PDP effectiveness may be due to their stability and different mechanism of action, as reported by others. Inhibition of proinflamatory cytokines is an interesting pharmacological aim to treat cirrhosis. Drug Dev. Res. 54:209–218, 2001. © 2002 Wiley‐Liss, Inc.</description><subject>Biological and medical sciences</subject><subject>cirrhosis</subject><subject>citokines</subject><subject>Digestive system</subject><subject>liver</subject><subject>Medical sciences</subject><subject>Pharmacology. 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Drug treatments</topic><topic>thalidomide</topic><topic>TNF-α</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fernández-Martínez, Eduardo</creatorcontrib><creatorcontrib>Morales-Ríos, Martha S.</creatorcontrib><creatorcontrib>Pérez-Álvarez, Víctor</creatorcontrib><creatorcontrib>Muriel, Pablo</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Drug development research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fernández-Martínez, Eduardo</au><au>Morales-Ríos, Martha S.</au><au>Pérez-Álvarez, Víctor</au><au>Muriel, Pablo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of thalidomide and 3-phthalimido-3-(3,4-dimethoxyphenyl)-propanamide on bile duct obstruction-induced cirrhosis in the rat</atitle><jtitle>Drug development research</jtitle><addtitle>Drug Dev. Res</addtitle><date>2001-12</date><risdate>2001</risdate><volume>54</volume><issue>4</issue><spage>209</spage><epage>218</epage><pages>209-218</pages><issn>0272-4391</issn><eissn>1098-2299</eissn><coden>DDREDK</coden><abstract>Tumor necrosis factor‐alpha (TNF‐α) plays a central role in cellular necrosis, apoptosis, organ failure, tissue damage, inflammation, and fibrosis. These processes, occurring in liver injury, may lead to cirrhosis. Thalidomide and its analogs have shown to be effective TNF‐α inhibitors. The aim of this work was to synthesize a thalidomide analog, the 3‐phthalimido‐3‐(3,4‐dimethoxyphenyl)‐propanamide (PDP) and to evaluate its hepatoprotective properties on bile duct obstruction‐induced cirrhosis. Synthesis, purification, and spectroscopic characterization of PDP were carried out. Thalidomide (200 mg/kg) or PDP (15 mg/kg) were administered to sham (Sh) or bile duct ligated (BDL) rats. The animals were sacrificed 28 days after treatments. Alkaline phosphatase (Alk. Phosph.), γ‐glutamyl transpeptidase (γ‐GTP) and alanine aminotransferase (ALT) enzyme activities, bilirubins, and TNF‐α concentrations were evaluated in plasma. Collagen was estimated by the liver hydroxyproline content and histopathology was performed. Both drugs showed partial amelioration of cirrhosis. However, the hepatoprotective effects of thalidomide were poor when compared to those afforded by PDP. While PDP improved the majority of the biochemical markers of liver injury and prevented partial but significantly collagen accumulation, thalidomide showed only modest beneficial effects on bilirubins and ALT. PDP was effective in preventing the increase in plasma TNF‐α levels, while thalidomide not only failed to inhibit TNF‐α, but increased it. Differences between thalidomide and PDP effectiveness may be due to their stability and different mechanism of action, as reported by others. Inhibition of proinflamatory cytokines is an interesting pharmacological aim to treat cirrhosis. Drug Dev. Res. 54:209–218, 2001. © 2002 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/ddr.10022</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences cirrhosis citokines Digestive system liver Medical sciences Pharmacology. Drug treatments thalidomide TNF-α |
title | Effects of thalidomide and 3-phthalimido-3-(3,4-dimethoxyphenyl)-propanamide on bile duct obstruction-induced cirrhosis in the rat |
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