Neuroinflammation and cognitive function in aged mice following minor surgery
Following surgery, elderly patients often suffer from postoperative cognitive dysfunction (POCD) which can persist long after physical recovery. It is known that surgery-induced tissue damage activates the peripheral innate immune system resulting in the release of inflammatory mediators. Compared t...
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Veröffentlicht in: | Experimental gerontology 2008-09, Vol.43 (9), p.840-846 |
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description | Following surgery, elderly patients often suffer from postoperative cognitive dysfunction (POCD) which can persist long after physical recovery. It is known that surgery-induced tissue damage activates the peripheral innate immune system resulting in the release of inflammatory mediators. Compared to adults, aged animals demonstrate increased neuroinflammation and microglial priming that leads to an exaggerated proinflammatory cytokine response following activation of the peripheral immune system. Therefore, we sought to determine if the immune response to surgical trauma results in increased neuroinflammation and cognitive impairment in aged mice. Adult and aged mice underwent minor abdominal surgery and 24
h later hippocampal cytokines were measured and working memory was assessed in a reversal learning version of the Morris water maze. While adult mice showed no signs of neuroinflammation following surgery, aged mice had significantly increased levels of IL-1β mRNA in the hippocampus. Minor surgery did not result in severe cognitive impairment although aged mice that underwent surgery did tend to perseverate in the old target during reversal testing suggesting reduced cognitive flexibility. Overall these results suggest that minor surgery leads to an exaggerated neuroinflammatory response in aged mice but does not result in significantly impaired performance in the Morris water maze. |
doi_str_mv | 10.1016/j.exger.2008.06.004 |
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h later hippocampal cytokines were measured and working memory was assessed in a reversal learning version of the Morris water maze. While adult mice showed no signs of neuroinflammation following surgery, aged mice had significantly increased levels of IL-1β mRNA in the hippocampus. Minor surgery did not result in severe cognitive impairment although aged mice that underwent surgery did tend to perseverate in the old target during reversal testing suggesting reduced cognitive flexibility. Overall these results suggest that minor surgery leads to an exaggerated neuroinflammatory response in aged mice but does not result in significantly impaired performance in the Morris water maze.</description><identifier>ISSN: 0531-5565</identifier><identifier>EISSN: 1873-6815</identifier><identifier>DOI: 10.1016/j.exger.2008.06.004</identifier><identifier>PMID: 18602982</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Aging ; Aging - immunology ; Aging - physiology ; Aging - psychology ; Analgesics - pharmacology ; Anesthetics - pharmacology ; Animals ; Brain ; Cognition Disorders - immunology ; Cytokines ; Cytokines - biosynthesis ; Cytokines - genetics ; Hippocampus - drug effects ; Hippocampus - immunology ; Interleukin-1beta - biosynthesis ; Interleukin-1beta - genetics ; Male ; Maze Learning ; Memory, Short-Term ; Mice ; Mice, Inbred BALB C ; Minor Surgical Procedures ; Motor Activity ; Neurogenic Inflammation - immunology ; Neurogenic Inflammation - psychology ; Neuroimmunomodulation ; POCD ; Postoperative Complications - immunology ; RNA, Messenger - genetics ; Working memory</subject><ispartof>Experimental gerontology, 2008-09, Vol.43 (9), p.840-846</ispartof><rights>2008 Elsevier Inc.</rights><rights>2008 Elsevier Inc. All rights reserved. 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-e19f8d1aca5e1e8edade51cf86bfcc120b49ed368859cf954c0c6b32916f67e3</citedby><cites>FETCH-LOGICAL-c488t-e19f8d1aca5e1e8edade51cf86bfcc120b49ed368859cf954c0c6b32916f67e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.exger.2008.06.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,777,781,882,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18602982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rosczyk, H.A.</creatorcontrib><creatorcontrib>Sparkman, N.L.</creatorcontrib><creatorcontrib>Johnson, R.W.</creatorcontrib><title>Neuroinflammation and cognitive function in aged mice following minor surgery</title><title>Experimental gerontology</title><addtitle>Exp Gerontol</addtitle><description>Following surgery, elderly patients often suffer from postoperative cognitive dysfunction (POCD) which can persist long after physical recovery. It is known that surgery-induced tissue damage activates the peripheral innate immune system resulting in the release of inflammatory mediators. Compared to adults, aged animals demonstrate increased neuroinflammation and microglial priming that leads to an exaggerated proinflammatory cytokine response following activation of the peripheral immune system. Therefore, we sought to determine if the immune response to surgical trauma results in increased neuroinflammation and cognitive impairment in aged mice. Adult and aged mice underwent minor abdominal surgery and 24
h later hippocampal cytokines were measured and working memory was assessed in a reversal learning version of the Morris water maze. While adult mice showed no signs of neuroinflammation following surgery, aged mice had significantly increased levels of IL-1β mRNA in the hippocampus. Minor surgery did not result in severe cognitive impairment although aged mice that underwent surgery did tend to perseverate in the old target during reversal testing suggesting reduced cognitive flexibility. Overall these results suggest that minor surgery leads to an exaggerated neuroinflammatory response in aged mice but does not result in significantly impaired performance in the Morris water maze.</description><subject>Aging</subject><subject>Aging - immunology</subject><subject>Aging - physiology</subject><subject>Aging - psychology</subject><subject>Analgesics - pharmacology</subject><subject>Anesthetics - pharmacology</subject><subject>Animals</subject><subject>Brain</subject><subject>Cognition Disorders - immunology</subject><subject>Cytokines</subject><subject>Cytokines - biosynthesis</subject><subject>Cytokines - genetics</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - immunology</subject><subject>Interleukin-1beta - biosynthesis</subject><subject>Interleukin-1beta - genetics</subject><subject>Male</subject><subject>Maze Learning</subject><subject>Memory, Short-Term</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Minor Surgical Procedures</subject><subject>Motor Activity</subject><subject>Neurogenic Inflammation - immunology</subject><subject>Neurogenic Inflammation - psychology</subject><subject>Neuroimmunomodulation</subject><subject>POCD</subject><subject>Postoperative Complications - immunology</subject><subject>RNA, Messenger - genetics</subject><subject>Working memory</subject><issn>0531-5565</issn><issn>1873-6815</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EokvhFyChnLgleJzYsQ8goYovqbSX3i2vMw5eJXaxky3997jdFR-X9mR55n3fGfsh5DXQBiiId7sGf42YGkapbKhoKO2ekA3Ivq2FBP6UbChvoeZc8BPyIucdpVSwFp6TE5CCMiXZhny_wDVFH9xk5tksPobKhKGycQx-8Xus3BrsfdmXzohDNXtbqnGa4o0PY7mGmKq8prLK7UvyzJkp46vjeUquPn-6Ovtan19--Xb28by2nZRLjaCcHMBYwxFQ4mAG5GCdFFtnLTC67RQOrZCSK-sU7yy1YtsyBcKJHttT8uEQe71uZxwshiWZSV8nP5t0q6Px-v9O8D_0GPea9VyoHkrA22NAij9XzIuefbY4TSZgXLMWqhM96-SjQlAcQDJehO1BaFPMOaH7sw1QfYdL7_Q9Ln2HS1OhC67ievPvQ_56jnyK4P1BgOU3977Ys_UYLA4-oV30EP2DA34D7ByqwA</recordid><startdate>20080901</startdate><enddate>20080901</enddate><creator>Rosczyk, H.A.</creator><creator>Sparkman, N.L.</creator><creator>Johnson, R.W.</creator><general>Elsevier Inc</general><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>7QO</scope><scope>7T5</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20080901</creationdate><title>Neuroinflammation and cognitive function in aged mice following minor surgery</title><author>Rosczyk, H.A. ; Sparkman, N.L. ; Johnson, R.W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-e19f8d1aca5e1e8edade51cf86bfcc120b49ed368859cf954c0c6b32916f67e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aging</topic><topic>Aging - immunology</topic><topic>Aging - physiology</topic><topic>Aging - psychology</topic><topic>Analgesics - pharmacology</topic><topic>Anesthetics - pharmacology</topic><topic>Animals</topic><topic>Brain</topic><topic>Cognition Disorders - immunology</topic><topic>Cytokines</topic><topic>Cytokines - biosynthesis</topic><topic>Cytokines - genetics</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - immunology</topic><topic>Interleukin-1beta - biosynthesis</topic><topic>Interleukin-1beta - genetics</topic><topic>Male</topic><topic>Maze Learning</topic><topic>Memory, Short-Term</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Minor Surgical Procedures</topic><topic>Motor Activity</topic><topic>Neurogenic Inflammation - immunology</topic><topic>Neurogenic Inflammation - psychology</topic><topic>Neuroimmunomodulation</topic><topic>POCD</topic><topic>Postoperative Complications - immunology</topic><topic>RNA, Messenger - genetics</topic><topic>Working memory</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rosczyk, H.A.</creatorcontrib><creatorcontrib>Sparkman, N.L.</creatorcontrib><creatorcontrib>Johnson, R.W.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences 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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Experimental gerontology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosczyk, H.A.</au><au>Sparkman, N.L.</au><au>Johnson, R.W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuroinflammation and cognitive function in aged mice following minor surgery</atitle><jtitle>Experimental gerontology</jtitle><addtitle>Exp Gerontol</addtitle><date>2008-09-01</date><risdate>2008</risdate><volume>43</volume><issue>9</issue><spage>840</spage><epage>846</epage><pages>840-846</pages><issn>0531-5565</issn><eissn>1873-6815</eissn><abstract>Following surgery, elderly patients often suffer from postoperative cognitive dysfunction (POCD) which can persist long after physical recovery. It is known that surgery-induced tissue damage activates the peripheral innate immune system resulting in the release of inflammatory mediators. Compared to adults, aged animals demonstrate increased neuroinflammation and microglial priming that leads to an exaggerated proinflammatory cytokine response following activation of the peripheral immune system. Therefore, we sought to determine if the immune response to surgical trauma results in increased neuroinflammation and cognitive impairment in aged mice. Adult and aged mice underwent minor abdominal surgery and 24
h later hippocampal cytokines were measured and working memory was assessed in a reversal learning version of the Morris water maze. While adult mice showed no signs of neuroinflammation following surgery, aged mice had significantly increased levels of IL-1β mRNA in the hippocampus. Minor surgery did not result in severe cognitive impairment although aged mice that underwent surgery did tend to perseverate in the old target during reversal testing suggesting reduced cognitive flexibility. Overall these results suggest that minor surgery leads to an exaggerated neuroinflammatory response in aged mice but does not result in significantly impaired performance in the Morris water maze.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>18602982</pmid><doi>10.1016/j.exger.2008.06.004</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aging Aging - immunology Aging - physiology Aging - psychology Analgesics - pharmacology Anesthetics - pharmacology Animals Brain Cognition Disorders - immunology Cytokines Cytokines - biosynthesis Cytokines - genetics Hippocampus - drug effects Hippocampus - immunology Interleukin-1beta - biosynthesis Interleukin-1beta - genetics Male Maze Learning Memory, Short-Term Mice Mice, Inbred BALB C Minor Surgical Procedures Motor Activity Neurogenic Inflammation - immunology Neurogenic Inflammation - psychology Neuroimmunomodulation POCD Postoperative Complications - immunology RNA, Messenger - genetics Working memory |
title | Neuroinflammation and cognitive function in aged mice following minor surgery |
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