Trypanosoma lewisi: Alterations in membrane function in the rat

DEAE-cellulose-purified Trypanosoma lewisi from 4-day (dividing trypanosomes) and 7-day (non-dividing trypanosomes) infections in rats were compared for initial uptake of glucose, leucine, and potassium. Glucose entered the parasitic cells by mediated (saturable) processes, whereas leucine and K + e...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Experimental parasitology 1979-08, Vol.48 (1), p.15-26
Hauptverfasser: Schraw, Wayne P., Vaughan, Gerald L.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 26
container_issue 1
container_start_page 15
container_title Experimental parasitology
container_volume 48
creator Schraw, Wayne P.
Vaughan, Gerald L.
description DEAE-cellulose-purified Trypanosoma lewisi from 4-day (dividing trypanosomes) and 7-day (non-dividing trypanosomes) infections in rats were compared for initial uptake of glucose, leucine, and potassium. Glucose entered the parasitic cells by mediated (saturable) processes, whereas leucine and K + entered by mediated processes and diffusion. Glucose entry was significantly elevated in 4-day cells ( V max 4.00 ± 1.02 nmoles/ 1 × 10 8 cells/min) with respect to 7-day cells ( V max 1.83 ± 0.62 nmoles 1 × 10 8 cells/min). Likewise, the affinity of the glucose carrier was significantly greater in 4-day cells ( K m = 0.30 ± 0.02 m M) than in 7-day cells ( K m = 0.59 ± 0.11 m M). When leucine and K + transport were compared in 4- and 7-day populations, significant elevations in the rate of entry ( V max) of both substrates were observed for 4-day cells; K m values for leucine and K + were not altered by the stage of infection. For leucine, the V max and K m for 4-day cells were 2.40 ± 0.50 nmoles/1 × 10 8 cells/30 sec and 78 ± 7 μ M, respectively; corresponding values in 7-day cells were 1.06 ± 0.02 nmoles/1 × 10 8 cells/30 sec and 66 ± 11 μ M. For K +, the V max and K m for 4-day cells were 15.97 ± 0.38 nmoles/1 × 10 8 cells/min and 1.2 m M, respectively; corresponding values in 7-day cells were 4.76 ± 1.82 nmoles/1 × 10 8 cells/min and 1.05 m M. The observed increase in the rate of K + entry into 4-day cells was attributable to enhanced influx; no significant difference in the rate of K + efflux was noted when 4- and 7-day cells were compared ( t 1 2 of K + leak for 4- and 7-day cells were 68.1 ± 9.3 and 67.9 ± 15.2 min, respectively). Potassium influx was ouabain insensitive. Membrane function in 7-day cells was not uniformly inhibited. No significant difference in the activity of the membrane-bound enzyme, 5′-nucleotidase, was observed when 4- and 7-day cells were compared.
doi_str_mv 10.1016/0014-4894(79)90050-X
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_74592154</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>001448947990050X</els_id><sourcerecordid>74592154</sourcerecordid><originalsourceid>FETCH-LOGICAL-c356t-ad6fc1e59f5cac1ca4a5d631132ef7d4a7bfa3b83061e38e0a7f9c5df83fcc983</originalsourceid><addsrcrecordid>eNp9kEtPwzAQhC3EqxT-QQ85ITgE7NiOYw6gquIlVeJSpN4sx1kLozyKnYD670lI1SOnlWZnRrsfQjOCbwgm6S3GhMUsk-xKyGuJMcfx-gBNCJY4ThiTh2iyt5yisxA-McYZSdgJOqYiS4WYoIeV32503YSm0lEJPy64u2hetuB165o6RK6OKqhyr2uIbFebQR3E9gOi3nOOjqwuA1zs5hS9Pz2uFi_x8u35dTFfxobytI11kVpDgEvLjTbEaKZ5kVJCaAJWFEyL3GqaZxSnBGgGWAsrDS9sRq0xMqNTdDn2bnzz1UFoVeWCgbLs72q6oATjMiGc9UY2Go1vQvBg1ca7SvutIlgN2NTARA1MlJDqD5ta97HZrr_LKyj2oZFTv74f19D_-O3Aq2Ac1AYK58G0qmjc__2_84p9NQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>74592154</pqid></control><display><type>article</type><title>Trypanosoma lewisi: Alterations in membrane function in the rat</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Schraw, Wayne P. ; Vaughan, Gerald L.</creator><creatorcontrib>Schraw, Wayne P. ; Vaughan, Gerald L.</creatorcontrib><description>DEAE-cellulose-purified Trypanosoma lewisi from 4-day (dividing trypanosomes) and 7-day (non-dividing trypanosomes) infections in rats were compared for initial uptake of glucose, leucine, and potassium. Glucose entered the parasitic cells by mediated (saturable) processes, whereas leucine and K + entered by mediated processes and diffusion. Glucose entry was significantly elevated in 4-day cells ( V max 4.00 ± 1.02 nmoles/ 1 × 10 8 cells/min) with respect to 7-day cells ( V max 1.83 ± 0.62 nmoles 1 × 10 8 cells/min). Likewise, the affinity of the glucose carrier was significantly greater in 4-day cells ( K m = 0.30 ± 0.02 m M) than in 7-day cells ( K m = 0.59 ± 0.11 m M). When leucine and K + transport were compared in 4- and 7-day populations, significant elevations in the rate of entry ( V max) of both substrates were observed for 4-day cells; K m values for leucine and K + were not altered by the stage of infection. For leucine, the V max and K m for 4-day cells were 2.40 ± 0.50 nmoles/1 × 10 8 cells/30 sec and 78 ± 7 μ M, respectively; corresponding values in 7-day cells were 1.06 ± 0.02 nmoles/1 × 10 8 cells/30 sec and 66 ± 11 μ M. For K +, the V max and K m for 4-day cells were 15.97 ± 0.38 nmoles/1 × 10 8 cells/min and 1.2 m M, respectively; corresponding values in 7-day cells were 4.76 ± 1.82 nmoles/1 × 10 8 cells/min and 1.05 m M. The observed increase in the rate of K + entry into 4-day cells was attributable to enhanced influx; no significant difference in the rate of K + efflux was noted when 4- and 7-day cells were compared ( t 1 2 of K + leak for 4- and 7-day cells were 68.1 ± 9.3 and 67.9 ± 15.2 min, respectively). Potassium influx was ouabain insensitive. Membrane function in 7-day cells was not uniformly inhibited. No significant difference in the activity of the membrane-bound enzyme, 5′-nucleotidase, was observed when 4- and 7-day cells were compared.</description><identifier>ISSN: 0014-4894</identifier><identifier>EISSN: 1090-2449</identifier><identifier>DOI: 10.1016/0014-4894(79)90050-X</identifier><identifier>PMID: 378677</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Ablastin ; Animals ; Antibodies - physiology ; Biological Transport, Active ; Cell Membrane - metabolism ; DEAE-cellulose chromatography ; Glucose ; Glucose - metabolism ; Hemoflagellate ; Kinetics ; Leucine ; Leucine - metabolism ; Male ; Membranes ; Metabolism ; Nucleotidases - metabolism ; Potassium ; Potassium - metabolism ; Protozoa, parasitic ; Rat ; Rats ; Transport ; Trypanosoma lewisi ; Trypanosoma lewisi - immunology ; Trypanosoma lewisi - metabolism ; Trypanosomiasis - immunology ; Trypanosomiasis - parasitology</subject><ispartof>Experimental parasitology, 1979-08, Vol.48 (1), p.15-26</ispartof><rights>1979</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-ad6fc1e59f5cac1ca4a5d631132ef7d4a7bfa3b83061e38e0a7f9c5df83fcc983</citedby><cites>FETCH-LOGICAL-c356t-ad6fc1e59f5cac1ca4a5d631132ef7d4a7bfa3b83061e38e0a7f9c5df83fcc983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0014-4894(79)90050-X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/378677$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schraw, Wayne P.</creatorcontrib><creatorcontrib>Vaughan, Gerald L.</creatorcontrib><title>Trypanosoma lewisi: Alterations in membrane function in the rat</title><title>Experimental parasitology</title><addtitle>Exp Parasitol</addtitle><description>DEAE-cellulose-purified Trypanosoma lewisi from 4-day (dividing trypanosomes) and 7-day (non-dividing trypanosomes) infections in rats were compared for initial uptake of glucose, leucine, and potassium. Glucose entered the parasitic cells by mediated (saturable) processes, whereas leucine and K + entered by mediated processes and diffusion. Glucose entry was significantly elevated in 4-day cells ( V max 4.00 ± 1.02 nmoles/ 1 × 10 8 cells/min) with respect to 7-day cells ( V max 1.83 ± 0.62 nmoles 1 × 10 8 cells/min). Likewise, the affinity of the glucose carrier was significantly greater in 4-day cells ( K m = 0.30 ± 0.02 m M) than in 7-day cells ( K m = 0.59 ± 0.11 m M). When leucine and K + transport were compared in 4- and 7-day populations, significant elevations in the rate of entry ( V max) of both substrates were observed for 4-day cells; K m values for leucine and K + were not altered by the stage of infection. For leucine, the V max and K m for 4-day cells were 2.40 ± 0.50 nmoles/1 × 10 8 cells/30 sec and 78 ± 7 μ M, respectively; corresponding values in 7-day cells were 1.06 ± 0.02 nmoles/1 × 10 8 cells/30 sec and 66 ± 11 μ M. For K +, the V max and K m for 4-day cells were 15.97 ± 0.38 nmoles/1 × 10 8 cells/min and 1.2 m M, respectively; corresponding values in 7-day cells were 4.76 ± 1.82 nmoles/1 × 10 8 cells/min and 1.05 m M. The observed increase in the rate of K + entry into 4-day cells was attributable to enhanced influx; no significant difference in the rate of K + efflux was noted when 4- and 7-day cells were compared ( t 1 2 of K + leak for 4- and 7-day cells were 68.1 ± 9.3 and 67.9 ± 15.2 min, respectively). Potassium influx was ouabain insensitive. Membrane function in 7-day cells was not uniformly inhibited. No significant difference in the activity of the membrane-bound enzyme, 5′-nucleotidase, was observed when 4- and 7-day cells were compared.</description><subject>Ablastin</subject><subject>Animals</subject><subject>Antibodies - physiology</subject><subject>Biological Transport, Active</subject><subject>Cell Membrane - metabolism</subject><subject>DEAE-cellulose chromatography</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Hemoflagellate</subject><subject>Kinetics</subject><subject>Leucine</subject><subject>Leucine - metabolism</subject><subject>Male</subject><subject>Membranes</subject><subject>Metabolism</subject><subject>Nucleotidases - metabolism</subject><subject>Potassium</subject><subject>Potassium - metabolism</subject><subject>Protozoa, parasitic</subject><subject>Rat</subject><subject>Rats</subject><subject>Transport</subject><subject>Trypanosoma lewisi</subject><subject>Trypanosoma lewisi - immunology</subject><subject>Trypanosoma lewisi - metabolism</subject><subject>Trypanosomiasis - immunology</subject><subject>Trypanosomiasis - parasitology</subject><issn>0014-4894</issn><issn>1090-2449</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1979</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtPwzAQhC3EqxT-QQ85ITgE7NiOYw6gquIlVeJSpN4sx1kLozyKnYD670lI1SOnlWZnRrsfQjOCbwgm6S3GhMUsk-xKyGuJMcfx-gBNCJY4ThiTh2iyt5yisxA-McYZSdgJOqYiS4WYoIeV32503YSm0lEJPy64u2hetuB165o6RK6OKqhyr2uIbFebQR3E9gOi3nOOjqwuA1zs5hS9Pz2uFi_x8u35dTFfxobytI11kVpDgEvLjTbEaKZ5kVJCaAJWFEyL3GqaZxSnBGgGWAsrDS9sRq0xMqNTdDn2bnzz1UFoVeWCgbLs72q6oATjMiGc9UY2Go1vQvBg1ca7SvutIlgN2NTARA1MlJDqD5ta97HZrr_LKyj2oZFTv74f19D_-O3Aq2Ac1AYK58G0qmjc__2_84p9NQ</recordid><startdate>197908</startdate><enddate>197908</enddate><creator>Schraw, Wayne P.</creator><creator>Vaughan, Gerald L.</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>197908</creationdate><title>Trypanosoma lewisi: Alterations in membrane function in the rat</title><author>Schraw, Wayne P. ; Vaughan, Gerald L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-ad6fc1e59f5cac1ca4a5d631132ef7d4a7bfa3b83061e38e0a7f9c5df83fcc983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1979</creationdate><topic>Ablastin</topic><topic>Animals</topic><topic>Antibodies - physiology</topic><topic>Biological Transport, Active</topic><topic>Cell Membrane - metabolism</topic><topic>DEAE-cellulose chromatography</topic><topic>Glucose</topic><topic>Glucose - metabolism</topic><topic>Hemoflagellate</topic><topic>Kinetics</topic><topic>Leucine</topic><topic>Leucine - metabolism</topic><topic>Male</topic><topic>Membranes</topic><topic>Metabolism</topic><topic>Nucleotidases - metabolism</topic><topic>Potassium</topic><topic>Potassium - metabolism</topic><topic>Protozoa, parasitic</topic><topic>Rat</topic><topic>Rats</topic><topic>Transport</topic><topic>Trypanosoma lewisi</topic><topic>Trypanosoma lewisi - immunology</topic><topic>Trypanosoma lewisi - metabolism</topic><topic>Trypanosomiasis - immunology</topic><topic>Trypanosomiasis - parasitology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schraw, Wayne P.</creatorcontrib><creatorcontrib>Vaughan, Gerald L.</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>Experimental parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schraw, Wayne P.</au><au>Vaughan, Gerald L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trypanosoma lewisi: Alterations in membrane function in the rat</atitle><jtitle>Experimental parasitology</jtitle><addtitle>Exp Parasitol</addtitle><date>1979-08</date><risdate>1979</risdate><volume>48</volume><issue>1</issue><spage>15</spage><epage>26</epage><pages>15-26</pages><issn>0014-4894</issn><eissn>1090-2449</eissn><abstract>DEAE-cellulose-purified Trypanosoma lewisi from 4-day (dividing trypanosomes) and 7-day (non-dividing trypanosomes) infections in rats were compared for initial uptake of glucose, leucine, and potassium. Glucose entered the parasitic cells by mediated (saturable) processes, whereas leucine and K + entered by mediated processes and diffusion. Glucose entry was significantly elevated in 4-day cells ( V max 4.00 ± 1.02 nmoles/ 1 × 10 8 cells/min) with respect to 7-day cells ( V max 1.83 ± 0.62 nmoles 1 × 10 8 cells/min). Likewise, the affinity of the glucose carrier was significantly greater in 4-day cells ( K m = 0.30 ± 0.02 m M) than in 7-day cells ( K m = 0.59 ± 0.11 m M). When leucine and K + transport were compared in 4- and 7-day populations, significant elevations in the rate of entry ( V max) of both substrates were observed for 4-day cells; K m values for leucine and K + were not altered by the stage of infection. For leucine, the V max and K m for 4-day cells were 2.40 ± 0.50 nmoles/1 × 10 8 cells/30 sec and 78 ± 7 μ M, respectively; corresponding values in 7-day cells were 1.06 ± 0.02 nmoles/1 × 10 8 cells/30 sec and 66 ± 11 μ M. For K +, the V max and K m for 4-day cells were 15.97 ± 0.38 nmoles/1 × 10 8 cells/min and 1.2 m M, respectively; corresponding values in 7-day cells were 4.76 ± 1.82 nmoles/1 × 10 8 cells/min and 1.05 m M. The observed increase in the rate of K + entry into 4-day cells was attributable to enhanced influx; no significant difference in the rate of K + efflux was noted when 4- and 7-day cells were compared ( t 1 2 of K + leak for 4- and 7-day cells were 68.1 ± 9.3 and 67.9 ± 15.2 min, respectively). Potassium influx was ouabain insensitive. Membrane function in 7-day cells was not uniformly inhibited. No significant difference in the activity of the membrane-bound enzyme, 5′-nucleotidase, was observed when 4- and 7-day cells were compared.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>378677</pmid><doi>10.1016/0014-4894(79)90050-X</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0014-4894
ispartof Experimental parasitology, 1979-08, Vol.48 (1), p.15-26
issn 0014-4894
1090-2449
language eng
recordid cdi_proquest_miscellaneous_74592154
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Ablastin
Animals
Antibodies - physiology
Biological Transport, Active
Cell Membrane - metabolism
DEAE-cellulose chromatography
Glucose
Glucose - metabolism
Hemoflagellate
Kinetics
Leucine
Leucine - metabolism
Male
Membranes
Metabolism
Nucleotidases - metabolism
Potassium
Potassium - metabolism
Protozoa, parasitic
Rat
Rats
Transport
Trypanosoma lewisi
Trypanosoma lewisi - immunology
Trypanosoma lewisi - metabolism
Trypanosomiasis - immunology
Trypanosomiasis - parasitology
title Trypanosoma lewisi: Alterations in membrane function in the rat
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T11%3A58%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Trypanosoma%20lewisi:%20Alterations%20in%20membrane%20function%20in%20the%20rat&rft.jtitle=Experimental%20parasitology&rft.au=Schraw,%20Wayne%20P.&rft.date=1979-08&rft.volume=48&rft.issue=1&rft.spage=15&rft.epage=26&rft.pages=15-26&rft.issn=0014-4894&rft.eissn=1090-2449&rft_id=info:doi/10.1016/0014-4894(79)90050-X&rft_dat=%3Cproquest_cross%3E74592154%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=74592154&rft_id=info:pmid/378677&rft_els_id=001448947990050X&rfr_iscdi=true