An oral adsorbent ameliorates renal overload of indoxyl sulfate and progression of renal failure in diabetic rats
Otsuka Long-Evans Tokushima Fatty (OLETF) rats were established as a new model of non–insulin-dependent diabetes mellitus. An oral adsorbent, AST-120, is effective in removing such uremic toxins as indoxyl sulfate and delays the progression of chronic renal failure (CRF). This study was designed to...
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description | Otsuka Long-Evans Tokushima Fatty (OLETF) rats were established as a new model of non–insulin-dependent diabetes mellitus. An oral adsorbent, AST-120, is effective in removing such uremic toxins as indoxyl sulfate and delays the progression of chronic renal failure (CRF). This study was designed to determine the effects of AST-120 on the progression of CRF in uninephrectomized OLETF (1/2NxOLETF) rats and the localization of indoxyl sulfate in their kidneys. Four weeks after unilateral nephrectomy, 14 OLETF rats were divided into two groups; AST-120–administered and control 1/2NxOLETF rats. Long-Evans Tokushima Otsuka rats, which are genetically similar to the OLETF rats but not diabetic, were also included. After the administration of AST-120 for 36 weeks, we examined the effects of AST-120 on renal functional and pathological changes in the three groups. The control 1/2NxOLETF rats showed marked hyperglycemia, hyperlipidemia, renal failure, glomerular sclerosis, and tubulointerstitial injury. The administration of AST-120 to the 1/2NxOLETF rats retarded the progression of renal dysfunction and fibrosis, as well as hyperlipidemia, and reduced serum and urinary levels of indoxyl sulfate. Immunohistochemistry showed that AST-120 markedly reduced the overload of indoxyl sulfate in tubular epithelial cells, especially dilated tubules, of the 1/2NxOLETF rats. In conclusion, AST-120 delayed the progression of renal failure and fibrosis in 1/2NxOLETF rats and decreased the overload of indoxyl sulfate on renal tubular cells. |
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An oral adsorbent, AST-120, is effective in removing such uremic toxins as indoxyl sulfate and delays the progression of chronic renal failure (CRF). This study was designed to determine the effects of AST-120 on the progression of CRF in uninephrectomized OLETF (1/2NxOLETF) rats and the localization of indoxyl sulfate in their kidneys. Four weeks after unilateral nephrectomy, 14 OLETF rats were divided into two groups; AST-120–administered and control 1/2NxOLETF rats. Long-Evans Tokushima Otsuka rats, which are genetically similar to the OLETF rats but not diabetic, were also included. After the administration of AST-120 for 36 weeks, we examined the effects of AST-120 on renal functional and pathological changes in the three groups. The control 1/2NxOLETF rats showed marked hyperglycemia, hyperlipidemia, renal failure, glomerular sclerosis, and tubulointerstitial injury. The administration of AST-120 to the 1/2NxOLETF rats retarded the progression of renal dysfunction and fibrosis, as well as hyperlipidemia, and reduced serum and urinary levels of indoxyl sulfate. Immunohistochemistry showed that AST-120 markedly reduced the overload of indoxyl sulfate in tubular epithelial cells, especially dilated tubules, of the 1/2NxOLETF rats. In conclusion, AST-120 delayed the progression of renal failure and fibrosis in 1/2NxOLETF rats and decreased the overload of indoxyl sulfate on renal tubular cells.</description><identifier>ISSN: 0272-6386</identifier><identifier>EISSN: 1523-6838</identifier><identifier>DOI: 10.1053/ajkd.2001.20731</identifier><identifier>PMID: 11158853</identifier><language>eng</language><publisher>Orlando, FL: Elsevier Inc</publisher><subject>Administration, Oral ; Animals ; Associated diseases and complications ; Biological and medical sciences ; Blood Urea Nitrogen ; Carbon - pharmacology ; Cholesterol - blood ; Creatinine - blood ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - metabolism ; Diabetes. Impaired glucose tolerance ; Diabetic Nephropathies - etiology ; Diabetic Nephropathies - metabolism ; Diabetic Nephropathies - prevention & control ; diabetic nephropathy ; Disease Progression ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Immunohistochemistry ; Indican - metabolism ; indoxyl sulfate ; Kidney - drug effects ; Kidney - metabolism ; Kidney - pathology ; Kidney Failure, Chronic - metabolism ; Kidney Failure, Chronic - prevention & control ; Kidney Glomerulus - drug effects ; Kidney Glomerulus - metabolism ; Kidney Glomerulus - pathology ; Kidneys ; Male ; Medical sciences ; Nephrology. Urinary tract diseases ; Oral adsorbent, AST-120 ; Otsuka Long-Evans Tokushima Fatty (OLETF) rats ; Oxides - pharmacology ; Rats ; Rats, Inbred OLETF ; Rats, Long-Evans ; Treatment Outcome ; Triglycerides - blood ; Urinary system involvement in other diseases. 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An oral adsorbent, AST-120, is effective in removing such uremic toxins as indoxyl sulfate and delays the progression of chronic renal failure (CRF). This study was designed to determine the effects of AST-120 on the progression of CRF in uninephrectomized OLETF (1/2NxOLETF) rats and the localization of indoxyl sulfate in their kidneys. Four weeks after unilateral nephrectomy, 14 OLETF rats were divided into two groups; AST-120–administered and control 1/2NxOLETF rats. Long-Evans Tokushima Otsuka rats, which are genetically similar to the OLETF rats but not diabetic, were also included. After the administration of AST-120 for 36 weeks, we examined the effects of AST-120 on renal functional and pathological changes in the three groups. The control 1/2NxOLETF rats showed marked hyperglycemia, hyperlipidemia, renal failure, glomerular sclerosis, and tubulointerstitial injury. The administration of AST-120 to the 1/2NxOLETF rats retarded the progression of renal dysfunction and fibrosis, as well as hyperlipidemia, and reduced serum and urinary levels of indoxyl sulfate. Immunohistochemistry showed that AST-120 markedly reduced the overload of indoxyl sulfate in tubular epithelial cells, especially dilated tubules, of the 1/2NxOLETF rats. In conclusion, AST-120 delayed the progression of renal failure and fibrosis in 1/2NxOLETF rats and decreased the overload of indoxyl sulfate on renal tubular cells.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Associated diseases and complications</subject><subject>Biological and medical sciences</subject><subject>Blood Urea Nitrogen</subject><subject>Carbon - pharmacology</subject><subject>Cholesterol - blood</subject><subject>Creatinine - blood</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Diabetic Nephropathies - etiology</subject><subject>Diabetic Nephropathies - metabolism</subject><subject>Diabetic Nephropathies - prevention & control</subject><subject>diabetic nephropathy</subject><subject>Disease Progression</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Immunohistochemistry</subject><subject>Indican - metabolism</subject><subject>indoxyl sulfate</subject><subject>Kidney - drug effects</subject><subject>Kidney - metabolism</subject><subject>Kidney - pathology</subject><subject>Kidney Failure, Chronic - metabolism</subject><subject>Kidney Failure, Chronic - prevention & control</subject><subject>Kidney Glomerulus - drug effects</subject><subject>Kidney Glomerulus - metabolism</subject><subject>Kidney Glomerulus - pathology</subject><subject>Kidneys</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Oral adsorbent, AST-120</subject><subject>Otsuka Long-Evans Tokushima Fatty (OLETF) rats</subject><subject>Oxides - pharmacology</subject><subject>Rats</subject><subject>Rats, Inbred OLETF</subject><subject>Rats, Long-Evans</subject><subject>Treatment Outcome</subject><subject>Triglycerides - blood</subject><subject>Urinary system involvement in other diseases. 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Impaired glucose tolerance</topic><topic>Diabetic Nephropathies - etiology</topic><topic>Diabetic Nephropathies - metabolism</topic><topic>Diabetic Nephropathies - prevention & control</topic><topic>diabetic nephropathy</topic><topic>Disease Progression</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Immunohistochemistry</topic><topic>Indican - metabolism</topic><topic>indoxyl sulfate</topic><topic>Kidney - drug effects</topic><topic>Kidney - metabolism</topic><topic>Kidney - pathology</topic><topic>Kidney Failure, Chronic - metabolism</topic><topic>Kidney Failure, Chronic - prevention & control</topic><topic>Kidney Glomerulus - drug effects</topic><topic>Kidney Glomerulus - metabolism</topic><topic>Kidney Glomerulus - pathology</topic><topic>Kidneys</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Oral adsorbent, AST-120</topic><topic>Otsuka Long-Evans Tokushima Fatty (OLETF) rats</topic><topic>Oxides - pharmacology</topic><topic>Rats</topic><topic>Rats, Inbred OLETF</topic><topic>Rats, Long-Evans</topic><topic>Treatment Outcome</topic><topic>Triglycerides - blood</topic><topic>Urinary system involvement in other diseases. Miscellaneous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aoyama, Isao</creatorcontrib><creatorcontrib>Niwa, Toshimitsu</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>American journal of kidney diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aoyama, Isao</au><au>Niwa, Toshimitsu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An oral adsorbent ameliorates renal overload of indoxyl sulfate and progression of renal failure in diabetic rats</atitle><jtitle>American journal of kidney diseases</jtitle><addtitle>Am J Kidney Dis</addtitle><date>2001-01</date><risdate>2001</risdate><volume>37</volume><issue>1</issue><spage>S7</spage><epage>S12</epage><pages>S7-S12</pages><issn>0272-6386</issn><eissn>1523-6838</eissn><abstract>Otsuka Long-Evans Tokushima Fatty (OLETF) rats were established as a new model of non–insulin-dependent diabetes mellitus. An oral adsorbent, AST-120, is effective in removing such uremic toxins as indoxyl sulfate and delays the progression of chronic renal failure (CRF). This study was designed to determine the effects of AST-120 on the progression of CRF in uninephrectomized OLETF (1/2NxOLETF) rats and the localization of indoxyl sulfate in their kidneys. Four weeks after unilateral nephrectomy, 14 OLETF rats were divided into two groups; AST-120–administered and control 1/2NxOLETF rats. Long-Evans Tokushima Otsuka rats, which are genetically similar to the OLETF rats but not diabetic, were also included. After the administration of AST-120 for 36 weeks, we examined the effects of AST-120 on renal functional and pathological changes in the three groups. The control 1/2NxOLETF rats showed marked hyperglycemia, hyperlipidemia, renal failure, glomerular sclerosis, and tubulointerstitial injury. The administration of AST-120 to the 1/2NxOLETF rats retarded the progression of renal dysfunction and fibrosis, as well as hyperlipidemia, and reduced serum and urinary levels of indoxyl sulfate. Immunohistochemistry showed that AST-120 markedly reduced the overload of indoxyl sulfate in tubular epithelial cells, especially dilated tubules, of the 1/2NxOLETF rats. In conclusion, AST-120 delayed the progression of renal failure and fibrosis in 1/2NxOLETF rats and decreased the overload of indoxyl sulfate on renal tubular cells.</abstract><cop>Orlando, FL</cop><pub>Elsevier Inc</pub><pmid>11158853</pmid><doi>10.1053/ajkd.2001.20731</doi></addata></record> |
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subjects | Administration, Oral Animals Associated diseases and complications Biological and medical sciences Blood Urea Nitrogen Carbon - pharmacology Cholesterol - blood Creatinine - blood Diabetes Mellitus, Type 2 - complications Diabetes Mellitus, Type 2 - metabolism Diabetes. Impaired glucose tolerance Diabetic Nephropathies - etiology Diabetic Nephropathies - metabolism Diabetic Nephropathies - prevention & control diabetic nephropathy Disease Progression Endocrine pancreas. Apud cells (diseases) Endocrinopathies Immunohistochemistry Indican - metabolism indoxyl sulfate Kidney - drug effects Kidney - metabolism Kidney - pathology Kidney Failure, Chronic - metabolism Kidney Failure, Chronic - prevention & control Kidney Glomerulus - drug effects Kidney Glomerulus - metabolism Kidney Glomerulus - pathology Kidneys Male Medical sciences Nephrology. Urinary tract diseases Oral adsorbent, AST-120 Otsuka Long-Evans Tokushima Fatty (OLETF) rats Oxides - pharmacology Rats Rats, Inbred OLETF Rats, Long-Evans Treatment Outcome Triglycerides - blood Urinary system involvement in other diseases. Miscellaneous |
title | An oral adsorbent ameliorates renal overload of indoxyl sulfate and progression of renal failure in diabetic rats |
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