Ulinastatin promotes T lymphocyte apoptosis in rats with severe acute pancreatitis via mitochondrial pathways
We explored the influence of ulinastatin on apoptosis of T lymphocytes in rats with severe acute pancreatitis (SAP) and the effect of ulinastatin on mitochondrial apoptosis pathways in spleen lymphocytes. Thirty-six Wistar rats were randomly divided into three groups (N = 12): a sham operated group,...
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description | We explored the influence of ulinastatin on apoptosis of T lymphocytes in rats with severe acute pancreatitis (SAP) and the effect of ulinastatin on mitochondrial apoptosis pathways in spleen lymphocytes. Thirty-six Wistar rats were randomly divided into three groups (N = 12): a sham operated group, a SAP group, and an ulinastatin-treated SAP group. The SAP model was established by injecting 5% sodium taurocholate into the intrapancreatobiliary duct. Study rats were sacrificed after 24 h, and splenic lymphocytes were then collected. CD4(+) and CD8(+) T lymphocytes were labeled by direct immune fluorescence assays; the percentage of apoptotic cells, mitochondrial membrane potential levels, and mitochondria permeability transition pore opening levels were measured by flow cytometry. In the ulinastatin-treated SAP group, the ratio of CD4(+)/CD8(+) T lymphocytes was significantly higher than that in the SAP group, and the apoptosis percentage of CD4(+) T lymphocytes was significantly decreased. The percentage of lymphocytes with an abnormal opening of the mitochondrial permeability transition pore and lymphocytes with decreased mitochondrial membrane potential in the ulinastatin-treated SAP group were significantly lower than that in the SAP group. Ulinastatin can directly enhance immunological function and attenuate immune suppression in SAP rats through inhibiting the apoptosis of CD4(+) T lymphocytes. These study findings demonstrate that therapeutic effects may occur through inhibiting the apoptosis induced by mitochondrial signaling pathways. |
doi_str_mv | 10.4238/2015.May.25.2 |
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Thirty-six Wistar rats were randomly divided into three groups (N = 12): a sham operated group, a SAP group, and an ulinastatin-treated SAP group. The SAP model was established by injecting 5% sodium taurocholate into the intrapancreatobiliary duct. Study rats were sacrificed after 24 h, and splenic lymphocytes were then collected. CD4(+) and CD8(+) T lymphocytes were labeled by direct immune fluorescence assays; the percentage of apoptotic cells, mitochondrial membrane potential levels, and mitochondria permeability transition pore opening levels were measured by flow cytometry. In the ulinastatin-treated SAP group, the ratio of CD4(+)/CD8(+) T lymphocytes was significantly higher than that in the SAP group, and the apoptosis percentage of CD4(+) T lymphocytes was significantly decreased. The percentage of lymphocytes with an abnormal opening of the mitochondrial permeability transition pore and lymphocytes with decreased mitochondrial membrane potential in the ulinastatin-treated SAP group were significantly lower than that in the SAP group. Ulinastatin can directly enhance immunological function and attenuate immune suppression in SAP rats through inhibiting the apoptosis of CD4(+) T lymphocytes. These study findings demonstrate that therapeutic effects may occur through inhibiting the apoptosis induced by mitochondrial signaling pathways.</description><identifier>ISSN: 1676-5680</identifier><identifier>EISSN: 1676-5680</identifier><identifier>DOI: 10.4238/2015.May.25.2</identifier><identifier>PMID: 26125748</identifier><language>eng</language><publisher>Brazil</publisher><subject>Animals ; Apoptosis - drug effects ; CD4-Positive T-Lymphocytes - drug effects ; CD8-Positive T-Lymphocytes - drug effects ; Disease Models, Animal ; Flow Cytometry ; Glycoproteins - administration & dosage ; Humans ; Male ; Membrane Potential, Mitochondrial - drug effects ; Mitochondria - drug effects ; Pancreatitis - drug therapy ; Pancreatitis - pathology ; Rats ; Spleen - drug effects</subject><ispartof>Genetics and molecular research, 2015-05, Vol.14 (2), p.5511-5518</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-e790fed56323a265fd02ba06e78d004edf199766ea04d3cba891bc33fda239343</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26125748$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, C L</creatorcontrib><creatorcontrib>Li, N</creatorcontrib><creatorcontrib>Ma, T</creatorcontrib><creatorcontrib>Zhang, P</creatorcontrib><creatorcontrib>You, S Y</creatorcontrib><title>Ulinastatin promotes T lymphocyte apoptosis in rats with severe acute pancreatitis via mitochondrial pathways</title><title>Genetics and molecular research</title><addtitle>Genet Mol Res</addtitle><description>We explored the influence of ulinastatin on apoptosis of T lymphocytes in rats with severe acute pancreatitis (SAP) and the effect of ulinastatin on mitochondrial apoptosis pathways in spleen lymphocytes. Thirty-six Wistar rats were randomly divided into three groups (N = 12): a sham operated group, a SAP group, and an ulinastatin-treated SAP group. The SAP model was established by injecting 5% sodium taurocholate into the intrapancreatobiliary duct. Study rats were sacrificed after 24 h, and splenic lymphocytes were then collected. CD4(+) and CD8(+) T lymphocytes were labeled by direct immune fluorescence assays; the percentage of apoptotic cells, mitochondrial membrane potential levels, and mitochondria permeability transition pore opening levels were measured by flow cytometry. In the ulinastatin-treated SAP group, the ratio of CD4(+)/CD8(+) T lymphocytes was significantly higher than that in the SAP group, and the apoptosis percentage of CD4(+) T lymphocytes was significantly decreased. The percentage of lymphocytes with an abnormal opening of the mitochondrial permeability transition pore and lymphocytes with decreased mitochondrial membrane potential in the ulinastatin-treated SAP group were significantly lower than that in the SAP group. Ulinastatin can directly enhance immunological function and attenuate immune suppression in SAP rats through inhibiting the apoptosis of CD4(+) T lymphocytes. These study findings demonstrate that therapeutic effects may occur through inhibiting the apoptosis induced by mitochondrial signaling pathways.</description><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>CD4-Positive T-Lymphocytes - drug effects</subject><subject>CD8-Positive T-Lymphocytes - drug effects</subject><subject>Disease Models, Animal</subject><subject>Flow Cytometry</subject><subject>Glycoproteins - administration & dosage</subject><subject>Humans</subject><subject>Male</subject><subject>Membrane Potential, Mitochondrial - drug effects</subject><subject>Mitochondria - drug effects</subject><subject>Pancreatitis - drug therapy</subject><subject>Pancreatitis - pathology</subject><subject>Rats</subject><subject>Spleen - drug effects</subject><issn>1676-5680</issn><issn>1676-5680</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTtPwzAURi0EgvIYWVFGlhQ_YscZUcVLArGU2bpxHNUoiYPttsq_x1ULYmO6V_qOjnTvh9A1wfOCMnlHMeHzN5jmlM_pEZoRUYqcC4mP_-xn6DyET4wpLyQ-RWdUEMrLQs5Q_9HZAUKEaIds9K530YRsmXVTP66cnqLJYHRjdMGGLCEeYsi2Nq6yYDbGp1SvEzPCoL1JkpiwjYWst9HplRsab6FLcVxtYQqX6KSFLpirw7xAH48Py8Vz_vr-9LK4f801EzzmpqxwaxouGGVABW8bTGvAwpSywbgwTUuqqhTCAC4apmuQFak1Y20DlFWsYBfodu9NF32tTYiqt0GbroPBuHVQpKSUCC4o_R8VFSNScskTmu9R7V0I3rRq9LYHPymC1a4MtStDpTIU5Wqnvjmo13Vvml_65_vsG7vPh4g</recordid><startdate>20150525</startdate><enddate>20150525</enddate><creator>Wang, C L</creator><creator>Li, N</creator><creator>Ma, T</creator><creator>Zhang, P</creator><creator>You, S Y</creator><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><scope>7T5</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20150525</creationdate><title>Ulinastatin promotes T lymphocyte apoptosis in rats with severe acute pancreatitis via mitochondrial pathways</title><author>Wang, C L ; Li, N ; Ma, T ; Zhang, P ; You, S Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-e790fed56323a265fd02ba06e78d004edf199766ea04d3cba891bc33fda239343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>CD4-Positive T-Lymphocytes - drug effects</topic><topic>CD8-Positive T-Lymphocytes - drug effects</topic><topic>Disease Models, Animal</topic><topic>Flow Cytometry</topic><topic>Glycoproteins - administration & dosage</topic><topic>Humans</topic><topic>Male</topic><topic>Membrane Potential, Mitochondrial - drug effects</topic><topic>Mitochondria - drug effects</topic><topic>Pancreatitis - drug therapy</topic><topic>Pancreatitis - pathology</topic><topic>Rats</topic><topic>Spleen - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, C L</creatorcontrib><creatorcontrib>Li, N</creatorcontrib><creatorcontrib>Ma, T</creatorcontrib><creatorcontrib>Zhang, P</creatorcontrib><creatorcontrib>You, S Y</creatorcontrib><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><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Genetics and molecular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, C L</au><au>Li, N</au><au>Ma, T</au><au>Zhang, P</au><au>You, S Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ulinastatin promotes T lymphocyte apoptosis in rats with severe acute pancreatitis via mitochondrial pathways</atitle><jtitle>Genetics and molecular research</jtitle><addtitle>Genet Mol Res</addtitle><date>2015-05-25</date><risdate>2015</risdate><volume>14</volume><issue>2</issue><spage>5511</spage><epage>5518</epage><pages>5511-5518</pages><issn>1676-5680</issn><eissn>1676-5680</eissn><abstract>We explored the influence of ulinastatin on apoptosis of T lymphocytes in rats with severe acute pancreatitis (SAP) and the effect of ulinastatin on mitochondrial apoptosis pathways in spleen lymphocytes. Thirty-six Wistar rats were randomly divided into three groups (N = 12): a sham operated group, a SAP group, and an ulinastatin-treated SAP group. The SAP model was established by injecting 5% sodium taurocholate into the intrapancreatobiliary duct. Study rats were sacrificed after 24 h, and splenic lymphocytes were then collected. CD4(+) and CD8(+) T lymphocytes were labeled by direct immune fluorescence assays; the percentage of apoptotic cells, mitochondrial membrane potential levels, and mitochondria permeability transition pore opening levels were measured by flow cytometry. In the ulinastatin-treated SAP group, the ratio of CD4(+)/CD8(+) T lymphocytes was significantly higher than that in the SAP group, and the apoptosis percentage of CD4(+) T lymphocytes was significantly decreased. The percentage of lymphocytes with an abnormal opening of the mitochondrial permeability transition pore and lymphocytes with decreased mitochondrial membrane potential in the ulinastatin-treated SAP group were significantly lower than that in the SAP group. Ulinastatin can directly enhance immunological function and attenuate immune suppression in SAP rats through inhibiting the apoptosis of CD4(+) T lymphocytes. These study findings demonstrate that therapeutic effects may occur through inhibiting the apoptosis induced by mitochondrial signaling pathways.</abstract><cop>Brazil</cop><pmid>26125748</pmid><doi>10.4238/2015.May.25.2</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis - drug effects CD4-Positive T-Lymphocytes - drug effects CD8-Positive T-Lymphocytes - drug effects Disease Models, Animal Flow Cytometry Glycoproteins - administration & dosage Humans Male Membrane Potential, Mitochondrial - drug effects Mitochondria - drug effects Pancreatitis - drug therapy Pancreatitis - pathology Rats Spleen - drug effects |
title | Ulinastatin promotes T lymphocyte apoptosis in rats with severe acute pancreatitis via mitochondrial pathways |
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