Effect of Casein and β-Casomorphins on Gastrointestinal Motility in Rats
The effect of bovine casein and synthetic β-casomorphins on the motility of rat gastrointestinal tract was studied by noninvasive techniques using the nonabsorbable marker 141Ce. Casein suspensions (CAS) or whey protein suspensions (WPS) were labeled with 141Ce and fed by gastric tube. Gastric empty...
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Veröffentlicht in: | The Journal of nutrition 1990-03, Vol.120 (3), p.252-257 |
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description | The effect of bovine casein and synthetic β-casomorphins on the motility of rat gastrointestinal tract was studied by noninvasive techniques using the nonabsorbable marker 141Ce. Casein suspensions (CAS) or whey protein suspensions (WPS) were labeled with 141Ce and fed by gastric tube. Gastric emptying rate (GER) as well as gastrointestinal transit time (GITT) of the tracer were significantly longer with feeding CAS compared to WPS. The differences between the CAS and the WPS groups were partly (GER) or completely (GITT) abolished by pretreating the animals with the specific opiate-receptor antagonist naloxone. It is assumed that opioid peptides released from casein during digestion slowed gastrointestinal motility by direct interaction with gut opiate receptors. To prove whether β-casomorphins, when given by gastric tube, can affect motility, different synthetic β-casomorphins in doses between 1 and 10 mg were added to the WPS. The β-casomorphin-4 (Tyr-Pro-Phe-Pro-NH2) showed no effect on GITT. The D-Ala substituted D-Ala-β-casomorphin-4 (Tyr-D-Ala-Phe-Pro-NH2) and D-Ala-β-casomorphin-5 (Tyr-D-Ala-Phe-D-Ala-Tyr-NH2), which are more resistant to proteolytic attack and have higher opioid potency than β-casomorphin-4, slowed GITT in a dose-dependent manner. |
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Casein suspensions (CAS) or whey protein suspensions (WPS) were labeled with 141Ce and fed by gastric tube. Gastric emptying rate (GER) as well as gastrointestinal transit time (GITT) of the tracer were significantly longer with feeding CAS compared to WPS. The differences between the CAS and the WPS groups were partly (GER) or completely (GITT) abolished by pretreating the animals with the specific opiate-receptor antagonist naloxone. It is assumed that opioid peptides released from casein during digestion slowed gastrointestinal motility by direct interaction with gut opiate receptors. To prove whether β-casomorphins, when given by gastric tube, can affect motility, different synthetic β-casomorphins in doses between 1 and 10 mg were added to the WPS. The β-casomorphin-4 (Tyr-Pro-Phe-Pro-NH2) showed no effect on GITT. The D-Ala substituted D-Ala-β-casomorphin-4 (Tyr-D-Ala-Phe-Pro-NH2) and D-Ala-β-casomorphin-5 (Tyr-D-Ala-Phe-D-Ala-Tyr-NH2), which are more resistant to proteolytic attack and have higher opioid potency than β-casomorphin-4, slowed GITT in a dose-dependent manner.</description><identifier>ISSN: 0022-3166</identifier><identifier>DOI: 10.1093/jn/120.3.252</identifier><identifier>PMID: 2319342</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Amino Acid Sequence ; Analysis of Variance ; Animals ; casein ; Caseins - pharmacology ; Endorphins - chemical synthesis ; Endorphins - pharmacology ; Female ; Gastric Emptying - drug effects ; gastrointestinal motility ; Gastrointestinal Motility - drug effects ; Gastrointestinal Transit - drug effects ; Kinetics ; Male ; Molecular Sequence Data ; naloxone ; Naloxone - pharmacology ; Rats ; Rats, Inbred Strains ; β-casomorphins</subject><ispartof>The Journal of nutrition, 1990-03, Vol.120 (3), p.252-257</ispartof><rights>1990 American Society for Nutrition.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-18f3794b9f2bcf9af6e64d6469ce7a5fac34434b90e7250ed01d426626cc34c73</citedby><cites>FETCH-LOGICAL-c371t-18f3794b9f2bcf9af6e64d6469ce7a5fac34434b90e7250ed01d426626cc34c73</cites></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/2319342$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Daniel, Hannelore</creatorcontrib><creatorcontrib>Vohwinkel, Margret</creatorcontrib><creatorcontrib>Rehner, Gertrud</creatorcontrib><title>Effect of Casein and β-Casomorphins on Gastrointestinal Motility in Rats</title><title>The Journal of nutrition</title><addtitle>J Nutr</addtitle><description>The effect of bovine casein and synthetic β-casomorphins on the motility of rat gastrointestinal tract was studied by noninvasive techniques using the nonabsorbable marker 141Ce. Casein suspensions (CAS) or whey protein suspensions (WPS) were labeled with 141Ce and fed by gastric tube. Gastric emptying rate (GER) as well as gastrointestinal transit time (GITT) of the tracer were significantly longer with feeding CAS compared to WPS. The differences between the CAS and the WPS groups were partly (GER) or completely (GITT) abolished by pretreating the animals with the specific opiate-receptor antagonist naloxone. It is assumed that opioid peptides released from casein during digestion slowed gastrointestinal motility by direct interaction with gut opiate receptors. To prove whether β-casomorphins, when given by gastric tube, can affect motility, different synthetic β-casomorphins in doses between 1 and 10 mg were added to the WPS. The β-casomorphin-4 (Tyr-Pro-Phe-Pro-NH2) showed no effect on GITT. The D-Ala substituted D-Ala-β-casomorphin-4 (Tyr-D-Ala-Phe-Pro-NH2) and D-Ala-β-casomorphin-5 (Tyr-D-Ala-Phe-D-Ala-Tyr-NH2), which are more resistant to proteolytic attack and have higher opioid potency than β-casomorphin-4, slowed GITT in a dose-dependent manner.</description><subject>Amino Acid Sequence</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>casein</subject><subject>Caseins - pharmacology</subject><subject>Endorphins - chemical synthesis</subject><subject>Endorphins - pharmacology</subject><subject>Female</subject><subject>Gastric Emptying - drug effects</subject><subject>gastrointestinal motility</subject><subject>Gastrointestinal Motility - drug effects</subject><subject>Gastrointestinal Transit - drug effects</subject><subject>Kinetics</subject><subject>Male</subject><subject>Molecular Sequence Data</subject><subject>naloxone</subject><subject>Naloxone - pharmacology</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>β-casomorphins</subject><issn>0022-3166</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkM1KAzEURrNQaq3u3AqzcuW0-WumWUqptaAIouuQZm4wZSapSSr0tXwQn8lIiytXl_CdfNx7ELoieEywZJONnxCKx2xMp_QEDTGmtGZEiDN0ntIGY0y4nA3QgDIiGadDtFpYCyZXwVZzncD5Svu2-v6qyyv0IW7fnU9V8NVSpxyD8xlSdl531VPIrnN5X5U_LzqnC3RqdZfg8jhH6O1-8Tp_qB-fl6v53WNtWENyTWaWNZKvpaVrY6W2AgRvBRfSQKOnVhvGOSs5hoZOMbSYtJwKQYUpiWnYCN0cercxfOzKNqp3yUDXaQ9hl1QjhRRYsALeHkATQ0oRrNpG1-u4VwSrX1tq41WxpZgqtgp-fezdrXto_-CjqpKLQw7luE8HUSXjwBtoXSwGVRvc_8U_34h59g</recordid><startdate>19900301</startdate><enddate>19900301</enddate><creator>Daniel, Hannelore</creator><creator>Vohwinkel, Margret</creator><creator>Rehner, Gertrud</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>7X8</scope></search><sort><creationdate>19900301</creationdate><title>Effect of Casein and β-Casomorphins on Gastrointestinal Motility in Rats</title><author>Daniel, Hannelore ; Vohwinkel, Margret ; Rehner, Gertrud</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-18f3794b9f2bcf9af6e64d6469ce7a5fac34434b90e7250ed01d426626cc34c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Amino Acid Sequence</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>casein</topic><topic>Caseins - pharmacology</topic><topic>Endorphins - chemical synthesis</topic><topic>Endorphins - pharmacology</topic><topic>Female</topic><topic>Gastric Emptying - drug effects</topic><topic>gastrointestinal motility</topic><topic>Gastrointestinal Motility - drug effects</topic><topic>Gastrointestinal Transit - drug effects</topic><topic>Kinetics</topic><topic>Male</topic><topic>Molecular Sequence Data</topic><topic>naloxone</topic><topic>Naloxone - pharmacology</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>β-casomorphins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Daniel, Hannelore</creatorcontrib><creatorcontrib>Vohwinkel, Margret</creatorcontrib><creatorcontrib>Rehner, Gertrud</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><jtitle>The Journal of nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Daniel, Hannelore</au><au>Vohwinkel, Margret</au><au>Rehner, Gertrud</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Casein and β-Casomorphins on Gastrointestinal Motility in Rats</atitle><jtitle>The Journal of nutrition</jtitle><addtitle>J Nutr</addtitle><date>1990-03-01</date><risdate>1990</risdate><volume>120</volume><issue>3</issue><spage>252</spage><epage>257</epage><pages>252-257</pages><issn>0022-3166</issn><abstract>The effect of bovine casein and synthetic β-casomorphins on the motility of rat gastrointestinal tract was studied by noninvasive techniques using the nonabsorbable marker 141Ce. Casein suspensions (CAS) or whey protein suspensions (WPS) were labeled with 141Ce and fed by gastric tube. Gastric emptying rate (GER) as well as gastrointestinal transit time (GITT) of the tracer were significantly longer with feeding CAS compared to WPS. The differences between the CAS and the WPS groups were partly (GER) or completely (GITT) abolished by pretreating the animals with the specific opiate-receptor antagonist naloxone. It is assumed that opioid peptides released from casein during digestion slowed gastrointestinal motility by direct interaction with gut opiate receptors. To prove whether β-casomorphins, when given by gastric tube, can affect motility, different synthetic β-casomorphins in doses between 1 and 10 mg were added to the WPS. The β-casomorphin-4 (Tyr-Pro-Phe-Pro-NH2) showed no effect on GITT. The D-Ala substituted D-Ala-β-casomorphin-4 (Tyr-D-Ala-Phe-Pro-NH2) and D-Ala-β-casomorphin-5 (Tyr-D-Ala-Phe-D-Ala-Tyr-NH2), which are more resistant to proteolytic attack and have higher opioid potency than β-casomorphin-4, slowed GITT in a dose-dependent manner.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>2319342</pmid><doi>10.1093/jn/120.3.252</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Analysis of Variance Animals casein Caseins - pharmacology Endorphins - chemical synthesis Endorphins - pharmacology Female Gastric Emptying - drug effects gastrointestinal motility Gastrointestinal Motility - drug effects Gastrointestinal Transit - drug effects Kinetics Male Molecular Sequence Data naloxone Naloxone - pharmacology Rats Rats, Inbred Strains β-casomorphins |
title | Effect of Casein and β-Casomorphins on Gastrointestinal Motility in Rats |
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