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Changes in Essential Fatty Acids and Ileal Genes Associated with Metabolizing Enzymes and Fatty Acid Transporters in Rodent Models of Cystic Fibrosis
Cystic fibrosis (CF), the result of mutations in the CF transmembrane conductance regulator (CFTR), causes essential fatty acid deficiency. The aim of this study was to characterize fatty acid handling in two rodent models of CF; one strain which harbors the loss of phenylalanine at position 508 (Ph...
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Published in: | International journal of molecular sciences 2023-04, Vol.24 (8), p.7194 |
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description | Cystic fibrosis (CF), the result of mutations in the CF transmembrane conductance regulator (CFTR), causes essential fatty acid deficiency. The aim of this study was to characterize fatty acid handling in two rodent models of CF; one strain which harbors the loss of phenylalanine at position 508 (Phe508del) in CFTR and the other lacks functional CFTR (510X). Fatty acid concentrations were determined using gas chromatography in serum from Phe508del and 510X rats. The relative expression of genes responsible for fatty acid transport and metabolism were quantified using real-time PCR. Ileal tissue morphology was assessed histologically. There was an age-dependent decrease in eicosapentaenoic acid and the linoleic acid:α-linolenic acid ratio, a genotype-dependent decrease in docosapentaenoic acid (n-3) and an increase in the arachidonic acid:docosahexaenoic acid ratio in Phe508del rat serum, which was not observed in 510X rats. In the ileum,
mRNA was increased in Phe508del rats but decreased in 510X rats. Further,
,
,
and
mRNA were increased in Phe508del rats only. As assessed by Sirius Red staining, collagen was increased in Phe508del and 510X ileum. Thus, CF rat models exhibit alterations in the concentration of circulating fatty acids, which may be due to altered transport and metabolism, in addition to fibrosis and microscopic structural changes in the ileum. |
doi_str_mv | 10.3390/ijms24087194 |
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mRNA was increased in Phe508del rats but decreased in 510X rats. Further,
,
,
and
mRNA were increased in Phe508del rats only. As assessed by Sirius Red staining, collagen was increased in Phe508del and 510X ileum. Thus, CF rat models exhibit alterations in the concentration of circulating fatty acids, which may be due to altered transport and metabolism, in addition to fibrosis and microscopic structural changes in the ileum.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms24087194</identifier><identifier>PMID: 37108362</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Analysis ; Animals ; Coenzyme A Ligases - metabolism ; Collagen ; Cystic fibrosis ; Cystic Fibrosis - metabolism ; Cystic Fibrosis Transmembrane Conductance Regulator - genetics ; Cystic Fibrosis Transmembrane Conductance Regulator - metabolism ; Enzymes ; Essential fatty acids ; fatty acids ; Fatty Acids, Essential ; Genes ; Genetic aspects ; Genotype ; intestine ; Monounsaturated fatty acids ; Physiological aspects ; Rats ; RNA ; Rodentia - metabolism</subject><ispartof>International journal of molecular sciences, 2023-04, Vol.24 (8), p.7194</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c475t-d9d8fe8cb7c9ff132626fa1d82c80c39c022f8299f3ac804ebe70349ea9fccf43</cites><orcidid>0000-0002-5320-7756 ; 0000-0003-1697-8890 ; 0000-0002-8762-4865 ; 0000-0002-6045-3998 ; 0000-0002-4003-4454 ; 0000-0003-1259-0661</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138779/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138779/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37108362$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shrestha, Nirajan</creatorcontrib><creatorcontrib>Rout-Pitt, Nathan</creatorcontrib><creatorcontrib>McCarron, Alexandra</creatorcontrib><creatorcontrib>Jackson, Courtney A</creatorcontrib><creatorcontrib>Bulmer, Andrew C</creatorcontrib><creatorcontrib>McAinch, Andrew J</creatorcontrib><creatorcontrib>Donnelley, Martin</creatorcontrib><creatorcontrib>Parsons, David W</creatorcontrib><creatorcontrib>Hryciw, Deanne H</creatorcontrib><title>Changes in Essential Fatty Acids and Ileal Genes Associated with Metabolizing Enzymes and Fatty Acid Transporters in Rodent Models of Cystic Fibrosis</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Cystic fibrosis (CF), the result of mutations in the CF transmembrane conductance regulator (CFTR), causes essential fatty acid deficiency. The aim of this study was to characterize fatty acid handling in two rodent models of CF; one strain which harbors the loss of phenylalanine at position 508 (Phe508del) in CFTR and the other lacks functional CFTR (510X). Fatty acid concentrations were determined using gas chromatography in serum from Phe508del and 510X rats. The relative expression of genes responsible for fatty acid transport and metabolism were quantified using real-time PCR. Ileal tissue morphology was assessed histologically. There was an age-dependent decrease in eicosapentaenoic acid and the linoleic acid:α-linolenic acid ratio, a genotype-dependent decrease in docosapentaenoic acid (n-3) and an increase in the arachidonic acid:docosahexaenoic acid ratio in Phe508del rat serum, which was not observed in 510X rats. In the ileum,
mRNA was increased in Phe508del rats but decreased in 510X rats. Further,
,
,
and
mRNA were increased in Phe508del rats only. As assessed by Sirius Red staining, collagen was increased in Phe508del and 510X ileum. Thus, CF rat models exhibit alterations in the concentration of circulating fatty acids, which may be due to altered transport and metabolism, in addition to fibrosis and microscopic structural changes in the ileum.</description><subject>Analysis</subject><subject>Animals</subject><subject>Coenzyme A Ligases - metabolism</subject><subject>Collagen</subject><subject>Cystic fibrosis</subject><subject>Cystic Fibrosis - metabolism</subject><subject>Cystic Fibrosis Transmembrane Conductance Regulator - genetics</subject><subject>Cystic Fibrosis Transmembrane Conductance Regulator - metabolism</subject><subject>Enzymes</subject><subject>Essential fatty acids</subject><subject>fatty acids</subject><subject>Fatty Acids, Essential</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genotype</subject><subject>intestine</subject><subject>Monounsaturated fatty acids</subject><subject>Physiological aspects</subject><subject>Rats</subject><subject>RNA</subject><subject>Rodentia - metabolism</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNptkk1vEzEQhlcIREvgxhlZ4sKBFH9s1vYJRVFSIrVCQuVseb3jjaNdO9gbUPo_-L843VISCflg6_U7z8zYUxRvCb5iTOJPbtsnWmLBiSyfFZekpHSKccWfn5wvilcpbTGmjM7ky-KCcYIFq-hl8Xux0b6FhJxHy5TAD053aKWH4YDmxjUJad-gdQdZvQafjfOUgnF6gAb9csMG3cKg69C5e-dbtPT3hx7GoH8QdBe1T7sQB4gPmb6FJmdCt3nrEgoWLQ5pcAatXB1Dcul18cLqLsGbx31SfF8t7xZfpjdfr9eL-c3UlHw2TBvZCAvC1NxIawmjFa2sJo2gRmDDpMGUWkGltExnpYQaOGalBC2tMbZkk2I9cpugt2oXXa_jQQXt1IMQYqt0zIV1oIghHLCkZX7zsoaqnlUMm1ltbQlSMJlZn0fWbl_30JjcYNTdGfT8xruNasNPRTBhgvMj4cMjIYYfe0iD6l0y0HXaQ9gnRQXmktAq-yfF-9Ha6lyb8zZkpDna1ZzPiKSCYp5dV_9x5dVA70zwYF3WzwI-jgEmf0OKYJ_KJ1gdp02dTlu2vztt-cn8d7zYH3SS0Z4</recordid><startdate>20230401</startdate><enddate>20230401</enddate><creator>Shrestha, Nirajan</creator><creator>Rout-Pitt, Nathan</creator><creator>McCarron, Alexandra</creator><creator>Jackson, Courtney A</creator><creator>Bulmer, Andrew C</creator><creator>McAinch, Andrew J</creator><creator>Donnelley, Martin</creator><creator>Parsons, David W</creator><creator>Hryciw, Deanne H</creator><general>MDPI AG</general><general>MDPI</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>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5320-7756</orcidid><orcidid>https://orcid.org/0000-0003-1697-8890</orcidid><orcidid>https://orcid.org/0000-0002-8762-4865</orcidid><orcidid>https://orcid.org/0000-0002-6045-3998</orcidid><orcidid>https://orcid.org/0000-0002-4003-4454</orcidid><orcidid>https://orcid.org/0000-0003-1259-0661</orcidid></search><sort><creationdate>20230401</creationdate><title>Changes in Essential Fatty Acids and Ileal Genes Associated with Metabolizing Enzymes and Fatty Acid Transporters in Rodent Models of Cystic Fibrosis</title><author>Shrestha, Nirajan ; Rout-Pitt, Nathan ; McCarron, Alexandra ; Jackson, Courtney A ; Bulmer, Andrew C ; McAinch, Andrew J ; Donnelley, Martin ; Parsons, David W ; Hryciw, Deanne H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-d9d8fe8cb7c9ff132626fa1d82c80c39c022f8299f3ac804ebe70349ea9fccf43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Analysis</topic><topic>Animals</topic><topic>Coenzyme A Ligases - metabolism</topic><topic>Collagen</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - metabolism</topic><topic>Cystic Fibrosis Transmembrane Conductance Regulator - genetics</topic><topic>Cystic Fibrosis Transmembrane Conductance Regulator - metabolism</topic><topic>Enzymes</topic><topic>Essential fatty acids</topic><topic>fatty acids</topic><topic>Fatty Acids, Essential</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genotype</topic><topic>intestine</topic><topic>Monounsaturated fatty acids</topic><topic>Physiological aspects</topic><topic>Rats</topic><topic>RNA</topic><topic>Rodentia - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shrestha, Nirajan</creatorcontrib><creatorcontrib>Rout-Pitt, Nathan</creatorcontrib><creatorcontrib>McCarron, Alexandra</creatorcontrib><creatorcontrib>Jackson, Courtney A</creatorcontrib><creatorcontrib>Bulmer, Andrew C</creatorcontrib><creatorcontrib>McAinch, Andrew J</creatorcontrib><creatorcontrib>Donnelley, Martin</creatorcontrib><creatorcontrib>Parsons, David W</creatorcontrib><creatorcontrib>Hryciw, Deanne H</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>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shrestha, Nirajan</au><au>Rout-Pitt, Nathan</au><au>McCarron, Alexandra</au><au>Jackson, Courtney A</au><au>Bulmer, Andrew C</au><au>McAinch, Andrew J</au><au>Donnelley, Martin</au><au>Parsons, David W</au><au>Hryciw, Deanne H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in Essential Fatty Acids and Ileal Genes Associated with Metabolizing Enzymes and Fatty Acid Transporters in Rodent Models of Cystic Fibrosis</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2023-04-01</date><risdate>2023</risdate><volume>24</volume><issue>8</issue><spage>7194</spage><pages>7194-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Cystic fibrosis (CF), the result of mutations in the CF transmembrane conductance regulator (CFTR), causes essential fatty acid deficiency. The aim of this study was to characterize fatty acid handling in two rodent models of CF; one strain which harbors the loss of phenylalanine at position 508 (Phe508del) in CFTR and the other lacks functional CFTR (510X). Fatty acid concentrations were determined using gas chromatography in serum from Phe508del and 510X rats. The relative expression of genes responsible for fatty acid transport and metabolism were quantified using real-time PCR. Ileal tissue morphology was assessed histologically. There was an age-dependent decrease in eicosapentaenoic acid and the linoleic acid:α-linolenic acid ratio, a genotype-dependent decrease in docosapentaenoic acid (n-3) and an increase in the arachidonic acid:docosahexaenoic acid ratio in Phe508del rat serum, which was not observed in 510X rats. In the ileum,
mRNA was increased in Phe508del rats but decreased in 510X rats. Further,
,
,
and
mRNA were increased in Phe508del rats only. As assessed by Sirius Red staining, collagen was increased in Phe508del and 510X ileum. Thus, CF rat models exhibit alterations in the concentration of circulating fatty acids, which may be due to altered transport and metabolism, in addition to fibrosis and microscopic structural changes in the ileum.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37108362</pmid><doi>10.3390/ijms24087194</doi><orcidid>https://orcid.org/0000-0002-5320-7756</orcidid><orcidid>https://orcid.org/0000-0003-1697-8890</orcidid><orcidid>https://orcid.org/0000-0002-8762-4865</orcidid><orcidid>https://orcid.org/0000-0002-6045-3998</orcidid><orcidid>https://orcid.org/0000-0002-4003-4454</orcidid><orcidid>https://orcid.org/0000-0003-1259-0661</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Coenzyme A Ligases - metabolism Collagen Cystic fibrosis Cystic Fibrosis - metabolism Cystic Fibrosis Transmembrane Conductance Regulator - genetics Cystic Fibrosis Transmembrane Conductance Regulator - metabolism Enzymes Essential fatty acids fatty acids Fatty Acids, Essential Genes Genetic aspects Genotype intestine Monounsaturated fatty acids Physiological aspects Rats RNA Rodentia - metabolism |
title | Changes in Essential Fatty Acids and Ileal Genes Associated with Metabolizing Enzymes and Fatty Acid Transporters in Rodent Models of Cystic Fibrosis |
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