Protective Effect of Urinastatin on Ischemic Renal Injury in Rabbits
Protective effect of urinastatin on ischemic renal injury in rabbits was investigated by urinary enzymes and renal function tests. Ten rabbits were divided into two groups: the control group and urinastatin group administered 50, 000 units/kg of urinastatin. The ischemic renal injury model was made...
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Veröffentlicht in: | Nihon Jinzo Gakkai shi 1991, Vol.33(7), pp.673-677 |
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description | Protective effect of urinastatin on ischemic renal injury in rabbits was investigated by urinary enzymes and renal function tests. Ten rabbits were divided into two groups: the control group and urinastatin group administered 50, 000 units/kg of urinastatin. The ischemic renal injury model was made by occluding the left renal artery for 60 minutes. Urinary excretions of N-acetyl-β-Dglucosaminidase (NAG) and .A-glutamyl transpeptidase (γ-GTP) (U-NAG and U-γ-GTP), creatinine clearance (Ccr), free water clearance (CH2O), fractinal excretion of sodium (FENA) and urine volume (UV) were measured before occlusion of the left renal artery and after reflow. There were no significant differences in the values before occlusion (baseline values) for U-NAG, U-γ-GTP, Ccr, CH2O, FENa, and UV between the two groups. U-NAG after reflow was increased in the two groups compared with baseline values, and the increase was significantly lower in the urinastatin group than control group. U-γ-GTP after reflow was also increased in the two groups compared with baseline values, but the change was not significant between the two groups. Ccr and CH2O after reflow were significantly decreased, and FENa and UV were increased in the two groups compared with baseline values. However, no significant differences were observed between the two groups in these four parameters. These results suggest that urinastatin is effective for the protection of the kidney against ischemic damage, especially of the renal tubular cells. |
doi_str_mv | 10.14842/jpnjnephrol1959.33.673 |
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Ten rabbits were divided into two groups: the control group and urinastatin group administered 50, 000 units/kg of urinastatin. The ischemic renal injury model was made by occluding the left renal artery for 60 minutes. Urinary excretions of N-acetyl-β-Dglucosaminidase (NAG) and .A-glutamyl transpeptidase (γ-GTP) (U-NAG and U-γ-GTP), creatinine clearance (Ccr), free water clearance (CH2O), fractinal excretion of sodium (FENA) and urine volume (UV) were measured before occlusion of the left renal artery and after reflow. There were no significant differences in the values before occlusion (baseline values) for U-NAG, U-γ-GTP, Ccr, CH2O, FENa, and UV between the two groups. U-NAG after reflow was increased in the two groups compared with baseline values, and the increase was significantly lower in the urinastatin group than control group. U-γ-GTP after reflow was also increased in the two groups compared with baseline values, but the change was not significant between the two groups. Ccr and CH2O after reflow were significantly decreased, and FENa and UV were increased in the two groups compared with baseline values. However, no significant differences were observed between the two groups in these four parameters. These results suggest that urinastatin is effective for the protection of the kidney against ischemic damage, especially of the renal tubular cells.</description><identifier>ISSN: 0385-2385</identifier><identifier>EISSN: 1884-0728</identifier><identifier>DOI: 10.14842/jpnjnephrol1959.33.673</identifier><identifier>PMID: 1684217</identifier><language>jpn</language><publisher>Japan: Japanese Society of Nephrology</publisher><subject>Acetylglucosaminidase - urine ; Animals ; gamma-Glutamyltransferase - urine ; Glycoproteins - therapeutic use ; Ischemia - drug therapy ; Ischemia - prevention & control ; Kidney - blood supply ; N-acetyl-β-D-glucosaminidase (NAG) ; Rabbits ; renal ischemic ; urinastatin</subject><ispartof>The Japanese Journal of Nephrology, 1991, Vol.33(7), pp.673-677</ispartof><rights>Japanese Society of Nephrology</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1684217$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KIHARA, KAORU</creatorcontrib><creatorcontrib>NAGATA, NAOTO</creatorcontrib><creatorcontrib>TAKASAKI, MAYUMI</creatorcontrib><title>Protective Effect of Urinastatin on Ischemic Renal Injury in Rabbits</title><title>Nihon Jinzo Gakkai shi</title><addtitle>Jpn J Nephrol</addtitle><description>Protective effect of urinastatin on ischemic renal injury in rabbits was investigated by urinary enzymes and renal function tests. Ten rabbits were divided into two groups: the control group and urinastatin group administered 50, 000 units/kg of urinastatin. The ischemic renal injury model was made by occluding the left renal artery for 60 minutes. Urinary excretions of N-acetyl-β-Dglucosaminidase (NAG) and .A-glutamyl transpeptidase (γ-GTP) (U-NAG and U-γ-GTP), creatinine clearance (Ccr), free water clearance (CH2O), fractinal excretion of sodium (FENA) and urine volume (UV) were measured before occlusion of the left renal artery and after reflow. There were no significant differences in the values before occlusion (baseline values) for U-NAG, U-γ-GTP, Ccr, CH2O, FENa, and UV between the two groups. U-NAG after reflow was increased in the two groups compared with baseline values, and the increase was significantly lower in the urinastatin group than control group. U-γ-GTP after reflow was also increased in the two groups compared with baseline values, but the change was not significant between the two groups. Ccr and CH2O after reflow were significantly decreased, and FENa and UV were increased in the two groups compared with baseline values. However, no significant differences were observed between the two groups in these four parameters. These results suggest that urinastatin is effective for the protection of the kidney against ischemic damage, especially of the renal tubular cells.</description><subject>Acetylglucosaminidase - urine</subject><subject>Animals</subject><subject>gamma-Glutamyltransferase - urine</subject><subject>Glycoproteins - therapeutic use</subject><subject>Ischemia - drug therapy</subject><subject>Ischemia - prevention & control</subject><subject>Kidney - blood supply</subject><subject>N-acetyl-β-D-glucosaminidase (NAG)</subject><subject>Rabbits</subject><subject>renal ischemic</subject><subject>urinastatin</subject><issn>0385-2385</issn><issn>1884-0728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkF9LwzAUxYMoc8x9BLFPvnU2SZs_jzKnDgfKcM8hTW9dSpvOJBX27S1s-ODLuRd-hwPnIHSHswXORU4emoNrHBz2vm-xLOSC0gXj9AJNsRB5mnEiLtE0o6JIySjXaB6CLTMseEYLnk_QBLMxBvMpevrwfQQT7Q8kq7oev6Svk523Toeoo3VJ75J1MHvorEm24HSbrF0z-GMysq0uSxvDDbqqdRtgfr4ztHtefS5f0837y3r5uEkbkrOYUigKSrSUAiojmS6krHJRAsuIJjU1XJtK41xTyJnkteQVFoSXuKQMDHBJZ-j-lHvw_fcAIarOBgNtqx30Q1CcFIyKjI_G27NxKDuo1MHbTvujOtce-duJN2PJL_jj2kdrWlD_9lWUKn6SceY_l9lrr8DRX-AveTA</recordid><startdate>1991</startdate><enddate>1991</enddate><creator>KIHARA, KAORU</creator><creator>NAGATA, NAOTO</creator><creator>TAKASAKI, MAYUMI</creator><general>Japanese Society of Nephrology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>1991</creationdate><title>Protective Effect of Urinastatin on Ischemic Renal Injury in Rabbits</title><author>KIHARA, KAORU ; NAGATA, NAOTO ; TAKASAKI, MAYUMI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j246t-3e5532a998edc96a599d48be602a2f3c7acda14a3e4697f97d1827b1b36ece793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>1991</creationdate><topic>Acetylglucosaminidase - urine</topic><topic>Animals</topic><topic>gamma-Glutamyltransferase - urine</topic><topic>Glycoproteins - therapeutic use</topic><topic>Ischemia - drug therapy</topic><topic>Ischemia - prevention & control</topic><topic>Kidney - blood supply</topic><topic>N-acetyl-β-D-glucosaminidase (NAG)</topic><topic>Rabbits</topic><topic>renal ischemic</topic><topic>urinastatin</topic><toplevel>online_resources</toplevel><creatorcontrib>KIHARA, KAORU</creatorcontrib><creatorcontrib>NAGATA, NAOTO</creatorcontrib><creatorcontrib>TAKASAKI, MAYUMI</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Nihon Jinzo Gakkai shi</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KIHARA, KAORU</au><au>NAGATA, NAOTO</au><au>TAKASAKI, MAYUMI</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective Effect of Urinastatin on Ischemic Renal Injury in Rabbits</atitle><jtitle>Nihon Jinzo Gakkai shi</jtitle><addtitle>Jpn J Nephrol</addtitle><date>1991</date><risdate>1991</risdate><volume>33</volume><issue>7</issue><spage>673</spage><epage>677</epage><pages>673-677</pages><issn>0385-2385</issn><eissn>1884-0728</eissn><abstract>Protective effect of urinastatin on ischemic renal injury in rabbits was investigated by urinary enzymes and renal function tests. Ten rabbits were divided into two groups: the control group and urinastatin group administered 50, 000 units/kg of urinastatin. The ischemic renal injury model was made by occluding the left renal artery for 60 minutes. Urinary excretions of N-acetyl-β-Dglucosaminidase (NAG) and .A-glutamyl transpeptidase (γ-GTP) (U-NAG and U-γ-GTP), creatinine clearance (Ccr), free water clearance (CH2O), fractinal excretion of sodium (FENA) and urine volume (UV) were measured before occlusion of the left renal artery and after reflow. There were no significant differences in the values before occlusion (baseline values) for U-NAG, U-γ-GTP, Ccr, CH2O, FENa, and UV between the two groups. U-NAG after reflow was increased in the two groups compared with baseline values, and the increase was significantly lower in the urinastatin group than control group. U-γ-GTP after reflow was also increased in the two groups compared with baseline values, but the change was not significant between the two groups. Ccr and CH2O after reflow were significantly decreased, and FENa and UV were increased in the two groups compared with baseline values. However, no significant differences were observed between the two groups in these four parameters. These results suggest that urinastatin is effective for the protection of the kidney against ischemic damage, especially of the renal tubular cells.</abstract><cop>Japan</cop><pub>Japanese Society of Nephrology</pub><pmid>1684217</pmid><doi>10.14842/jpnjnephrol1959.33.673</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetylglucosaminidase - urine Animals gamma-Glutamyltransferase - urine Glycoproteins - therapeutic use Ischemia - drug therapy Ischemia - prevention & control Kidney - blood supply N-acetyl-β-D-glucosaminidase (NAG) Rabbits renal ischemic urinastatin |
title | Protective Effect of Urinastatin on Ischemic Renal Injury in Rabbits |
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