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...
Gespeichert in:
Veröffentlicht in: | Experimental parasitology 1979-08, Vol.48 (1), p.15-26 |
---|---|
Hauptverfasser: | , |
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 |