Transport of tyrosine and phenylalanine across the rat nasal mucosa

Transport of tyrosine (Tyr) and phenylalanine (Phe) across the rat nasal mucosa was studied using an in situ perfusion technique. It was found that both amino acids were absorbed by active, saturable transport processes. The Km and Vmax values were calculated to be 0.6 mM and 0.44 mM/hr for L-Tyr, a...

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Veröffentlicht in:Life sciences (1973) 1988, Vol.43 (7), p.585-593
Hauptverfasser: Tengamnuay, Parkpoom, Mitra, Ashim K.
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Mitra, Ashim K.
description Transport of tyrosine (Tyr) and phenylalanine (Phe) across the rat nasal mucosa was studied using an in situ perfusion technique. It was found that both amino acids were absorbed by active, saturable transport processes. The Km and Vmax values were calculated to be 0.6 mM and 0.44 mM/hr for L-Tyr, and 0.40 mM and 0.39 mM/hr for L-Phe, respectively. The values for L-Tyr agr agreed well with the results previously reported. When D-Tyr and D-Phe were used as substrates, the extent of nasal absorption was significantly reduced indicating the specific affinity of the carrier for the L-amino acids. When mixtures of L-Tyr and L-Phe were used as perfusates, both amino acids were found to be concomitantly absorbed in a competitive manner. This implied that at least one common carrier system was present in the nasal mucosa. In addition the transport appears to be Na +-dependent and may require metabolic energy as a driving force as seen from the inhibition of the L-Phe uptake by ouabain and 2,4-dinitrophenol.
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It was found that both amino acids were absorbed by active, saturable transport processes. The Km and Vmax values were calculated to be 0.6 mM and 0.44 mM/hr for L-Tyr, and 0.40 mM and 0.39 mM/hr for L-Phe, respectively. The values for L-Tyr agr agreed well with the results previously reported. When D-Tyr and D-Phe were used as substrates, the extent of nasal absorption was significantly reduced indicating the specific affinity of the carrier for the L-amino acids. When mixtures of L-Tyr and L-Phe were used as perfusates, both amino acids were found to be concomitantly absorbed in a competitive manner. This implied that at least one common carrier system was present in the nasal mucosa. In addition the transport appears to be Na +-dependent and may require metabolic energy as a driving force as seen from the inhibition of the L-Phe uptake by ouabain and 2,4-dinitrophenol.</description><subject>2,4-Dinitrophenol</subject><subject>Absorption</subject><subject>Air breathing</subject><subject>Animals</subject><subject>Binding, Competitive</subject><subject>Biological and medical sciences</subject><subject>Biological Transport - drug effects</subject><subject>Dinitrophenols - pharmacology</subject><subject>Energy Metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Kinetics</subject><subject>Male</subject><subject>mucosa</subject><subject>Nasal Mucosa - metabolism</subject><subject>nose</subject><subject>Ouabain - pharmacology</subject><subject>Perfusion</subject><subject>phenylalanine</subject><subject>Phenylalanine - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Respiratory system: anatomy, metabolism, gas exchange, ventilatory mechanics, respiratory hemodynamics</subject><subject>Sodium - pharmacology</subject><subject>Stereoisomerism</subject><subject>tyrosine</subject><subject>Tyrosine - metabolism</subject><subject>Vertebrates: respiratory system</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LAzEQhoMoWqv_QGEPInpYnSSbr4sgxS8oeNFziNkJrmx3a7IV-u9NP-hRTwPzvjPzzkPIGYUbClTeArCq5AzEldbXBkCyUu-REdXKlCA53SejneWIHKf0BQBCKH5IDjk3WlEYkclbdF2a93Eo-lAMy9inpsPCdXUx_8Ru2brWdeuOz1Iqhk8sohuKziXXFrOF75M7IQfBtQlPt3VM3h8f3ibP5fT16WVyPy19RdVQUi2FYLLiwB06zxAoq3KDGi-ckqidCUEFjxQ-jAyhkoblwIELL4SskY_J5WbvPPbfC0yDnTXJY5sTYr9IVmleGcOrf41UAGMsMxqTamNcPxcx2HlsZi4uLQW7gmxXBO2KoNXariFbncfOt_sXHzOsd0Nbqlm_2OouedeGjNg3aWdTXDHFV9fvNjbM0H4ajDb5BjuPdRPRD7bum79z_AInjZa3</recordid><startdate>1988</startdate><enddate>1988</enddate><creator>Tengamnuay, Parkpoom</creator><creator>Mitra, Ashim K.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>1988</creationdate><title>Transport of tyrosine and phenylalanine across the rat nasal mucosa</title><author>Tengamnuay, Parkpoom ; Mitra, Ashim K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-18655264303aeac2e012452619c5a76e8a9ff7fce10b96ff4692005f35c556de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>2,4-Dinitrophenol</topic><topic>Absorption</topic><topic>Air breathing</topic><topic>Animals</topic><topic>Binding, Competitive</topic><topic>Biological and medical sciences</topic><topic>Biological Transport - drug effects</topic><topic>Dinitrophenols - pharmacology</topic><topic>Energy Metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Kinetics</topic><topic>Male</topic><topic>mucosa</topic><topic>Nasal Mucosa - metabolism</topic><topic>nose</topic><topic>Ouabain - pharmacology</topic><topic>Perfusion</topic><topic>phenylalanine</topic><topic>Phenylalanine - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Respiratory system: anatomy, metabolism, gas exchange, ventilatory mechanics, respiratory hemodynamics</topic><topic>Sodium - pharmacology</topic><topic>Stereoisomerism</topic><topic>tyrosine</topic><topic>Tyrosine - metabolism</topic><topic>Vertebrates: respiratory system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tengamnuay, Parkpoom</creatorcontrib><creatorcontrib>Mitra, Ashim K.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tengamnuay, Parkpoom</au><au>Mitra, Ashim K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transport of tyrosine and phenylalanine across the rat nasal mucosa</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>1988</date><risdate>1988</risdate><volume>43</volume><issue>7</issue><spage>585</spage><epage>593</epage><pages>585-593</pages><issn>0024-3205</issn><eissn>1879-0631</eissn><coden>LIFSAK</coden><abstract>Transport of tyrosine (Tyr) and phenylalanine (Phe) across the rat nasal mucosa was studied using an in situ perfusion technique. It was found that both amino acids were absorbed by active, saturable transport processes. The Km and Vmax values were calculated to be 0.6 mM and 0.44 mM/hr for L-Tyr, and 0.40 mM and 0.39 mM/hr for L-Phe, respectively. The values for L-Tyr agr agreed well with the results previously reported. When D-Tyr and D-Phe were used as substrates, the extent of nasal absorption was significantly reduced indicating the specific affinity of the carrier for the L-amino acids. When mixtures of L-Tyr and L-Phe were used as perfusates, both amino acids were found to be concomitantly absorbed in a competitive manner. This implied that at least one common carrier system was present in the nasal mucosa. In addition the transport appears to be Na +-dependent and may require metabolic energy as a driving force as seen from the inhibition of the L-Phe uptake by ouabain and 2,4-dinitrophenol.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>3398710</pmid><doi>10.1016/0024-3205(88)90062-8</doi><tpages>9</tpages></addata></record>
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subjects 2,4-Dinitrophenol
Absorption
Air breathing
Animals
Binding, Competitive
Biological and medical sciences
Biological Transport - drug effects
Dinitrophenols - pharmacology
Energy Metabolism
Fundamental and applied biological sciences. Psychology
Kinetics
Male
mucosa
Nasal Mucosa - metabolism
nose
Ouabain - pharmacology
Perfusion
phenylalanine
Phenylalanine - metabolism
Rats
Rats, Inbred Strains
Respiratory system: anatomy, metabolism, gas exchange, ventilatory mechanics, respiratory hemodynamics
Sodium - pharmacology
Stereoisomerism
tyrosine
Tyrosine - metabolism
Vertebrates: respiratory system
title Transport of tyrosine and phenylalanine across the rat nasal mucosa
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