Neural Modulation of Gut Motility by Myomodulin Peptides and Acetylcholine in the Snail Lymnaea

Stephen J. Perry 1 , Volko A. Straub 1 , György Kemenes 1 , Niovi Santama 1 , Belinda M. Worster 1 , Julian F. Burke 2 , and Paul R. Benjamin 1 1  Sussex Centre for Neuroscience and 2  Department of Biochemistry, University of Sussex, Falmer, Brighton BN1 9QG, United Kingdom Perry, Stephen J., Volko...

Full description

Saved in:
Bibliographic Details
Published inJournal of neurophysiology Vol. 79; no. 5; pp. 2460 - 2474
Main Authors Perry, Stephen J, Straub, Volko A, Kemenes, Gyorgy, Santama, Niovi, Worster, Belinda M, Burke, Julian F, Benjamin, Paul R
Format Journal Article
LanguageEnglish
Published United States Am Phys Soc 01.05.1998
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Stephen J. Perry 1 , Volko A. Straub 1 , György Kemenes 1 , Niovi Santama 1 , Belinda M. Worster 1 , Julian F. Burke 2 , and Paul R. Benjamin 1 1  Sussex Centre for Neuroscience and 2  Department of Biochemistry, University of Sussex, Falmer, Brighton BN1 9QG, United Kingdom Perry, Stephen J., Volko A. Straub, György Kemenes, Niovi Santama, Belinda M. Worster, Julian F. Burke, and Paul R. Benjamin. Neural modulation of gut motility by myomodulin peptides and acetylcholine in the snail Lymnaea . J. Neurophysiol. 79: 2460-2474, 1998. Families of peptide neuromodulators are believed to play important roles in neural networks that control behaviors. Here, we investigate the expression and role of one such group of modulators, the myomodulins, in the feeding system of Lymnaea stagnalis . Using a combination of in situ hybridization and antibody staining, expression of the myomodulin gene was confirmed in a number of identified behaviorally significant neuronal types, including the paired B2 motor neurons. The B2 cells were shown to project axons to the proesophagus, where they modulate foregut contractile activity. The presence of the five myomodulin peptide structures was confirmed in the B2 cells, the proesophagus, and the intervening nerve by mass spectrometry. Using a sensitive cell culture assay, evidence that the B2 cells are cholinergic also is presented. Application of four of the five myomodulin peptides to the isolated foregut increased both contraction frequency and tonus, whereas the main effect of acetylcholine (ACh) application was a large tonal contraction. The fifth myomodulin peptide (pQIPMLRLamide) appeared to have little or no effect on gut motility. Coapplication of all five myomodulin peptides gave a greater increase in tonus than that produced by the peptides applied individually, suggesting that corelease of the peptides onto the gut would produce an enhanced response. The combined effects that the myomodulin peptides and ACh have on foregut motility can mimic the main actions of B2 cell stimulation.
AbstractList Stephen J. Perry 1 , Volko A. Straub 1 , György Kemenes 1 , Niovi Santama 1 , Belinda M. Worster 1 , Julian F. Burke 2 , and Paul R. Benjamin 1 1  Sussex Centre for Neuroscience and 2  Department of Biochemistry, University of Sussex, Falmer, Brighton BN1 9QG, United Kingdom Perry, Stephen J., Volko A. Straub, György Kemenes, Niovi Santama, Belinda M. Worster, Julian F. Burke, and Paul R. Benjamin. Neural modulation of gut motility by myomodulin peptides and acetylcholine in the snail Lymnaea . J. Neurophysiol. 79: 2460-2474, 1998. Families of peptide neuromodulators are believed to play important roles in neural networks that control behaviors. Here, we investigate the expression and role of one such group of modulators, the myomodulins, in the feeding system of Lymnaea stagnalis . Using a combination of in situ hybridization and antibody staining, expression of the myomodulin gene was confirmed in a number of identified behaviorally significant neuronal types, including the paired B2 motor neurons. The B2 cells were shown to project axons to the proesophagus, where they modulate foregut contractile activity. The presence of the five myomodulin peptide structures was confirmed in the B2 cells, the proesophagus, and the intervening nerve by mass spectrometry. Using a sensitive cell culture assay, evidence that the B2 cells are cholinergic also is presented. Application of four of the five myomodulin peptides to the isolated foregut increased both contraction frequency and tonus, whereas the main effect of acetylcholine (ACh) application was a large tonal contraction. The fifth myomodulin peptide (pQIPMLRLamide) appeared to have little or no effect on gut motility. Coapplication of all five myomodulin peptides gave a greater increase in tonus than that produced by the peptides applied individually, suggesting that corelease of the peptides onto the gut would produce an enhanced response. The combined effects that the myomodulin peptides and ACh have on foregut motility can mimic the main actions of B2 cell stimulation.
Perry, Stephen J., Volko A. Straub, György Kemenes, Niovi Santama, Belinda M. Worster, Julian F. Burke, and Paul R. Benjamin. Neural modulation of gut motility by myomodulin peptides and acetylcholine in the snail Lymnaea. J. Neurophysiol. 79: 2460–2474, 1998. Families of peptide neuromodulators are believed to play important roles in neural networks that control behaviors. Here, we investigate the expression and role of one such group of modulators, the myomodulins, in the feeding system of Lymnaea stagnalis. Using a combination of in situ hybridization and antibody staining, expression of the myomodulin gene was confirmed in a number of identified behaviorally significant neuronal types, including the paired B2 motor neurons. The B2 cells were shown to project axons to the proesophagus, where they modulate foregut contractile activity. The presence of the five myomodulin peptide structures was confirmed in the B2 cells, the proesophagus, and the intervening nerve by mass spectrometry. Using a sensitive cell culture assay, evidence that the B2 cells are cholinergic also is presented. Application of four of the five myomodulin peptides to the isolated foregut increased both contraction frequency and tonus, whereas the main effect of acetylcholine (ACh) application was a large tonal contraction. The fifth myomodulin peptide (pQIPMLRLamide) appeared to have little or no effect on gut motility. Coapplication of all five myomodulin peptides gave a greater increase in tonus than that produced by the peptides applied individually, suggesting that corelease of the peptides onto the gut would produce an enhanced response. The combined effects that the myomodulin peptides and ACh have on foregut motility can mimic the main actions of B2 cell stimulation.
Families of peptide neuromodulators are believed to play important roles in neural networks that control behaviors. Here, we investigate the expression and role of one such group of modulators, the myomodulins, in the feeding system of Lymnaea stagnalis. Using a combination of in situ hybridization and antibody staining, expression of the myomodulin gene was confirmed in a number of identified behaviorally significant neuronal types, including the paired B2 motor neurons. The B2 cells were shown to project axons to the proesophagus, where they modulate foregut contractile activity. The presence of the five myomodulin peptide structures was confirmed in the B2 cells, the proesophagus, and the intervening nerve by mass spectrometry. Using a sensitive cell culture assay, evidence that the B2 cells are cholinergic also is presented. Application of four of the five myomodulin peptides to the isolated foregut increased both contraction frequency and tonus, whereas the main effect of acetylcholine (ACh) application was a large tonal contraction. The fifth myomodulin peptide (pQIPMLRLamide) appeared to have little or no effect on gut motility. Coapplication of all five myomodulin peptides gave a greater increase in tonus than that produced by the peptides applied individually, suggesting that corelease of the peptides onto the gut would produce an enhanced response. The combined effects that the myomodulin peptides and ACh have on foregut motility can mimic the main actions of B2 cell stimulation.
Author Kemenes, Gyorgy
Benjamin, Paul R
Santama, Niovi
Burke, Julian F
Straub, Volko A
Perry, Stephen J
Worster, Belinda M
Author_xml – sequence: 1
  fullname: Perry, Stephen J
– sequence: 2
  fullname: Straub, Volko A
– sequence: 3
  fullname: Kemenes, Gyorgy
– sequence: 4
  fullname: Santama, Niovi
– sequence: 5
  fullname: Worster, Belinda M
– sequence: 6
  fullname: Burke, Julian F
– sequence: 7
  fullname: Benjamin, Paul R
BackLink https://www.ncbi.nlm.nih.gov/pubmed/9582220$$D View this record in MEDLINE/PubMed
BookMark eNqFkEtv3CAUhVGUKp2k-QFdVGLVrsbhYWyzjKK8pElaqekaYfs6ZoTBNVit_32xZpSuqq5A95zzcTnn6NR5Bwh9pCSjVLCrvcuolFVWykxkLC_ICdqkOdtSIatTtCEk3Tkpy_foPIQ9IaQUhJ2hMykqxhjZIPUM86QtfvLtbHU03mHf4fs5pkk01sQF1wt-WvywGozD32CMpoWAtWvxdQNxsU3vkwI4qbEH_N1pY_FuGZwG_QG967QNcHk8L9CPu9uXm4ft7uv94831btvkhMetrlrRNFwKLYXkRUEY5ZSn9QtZiFzQCrSsZc101YgKBLQEci7yrk7fKOo85xfo84E7Tv7nDCGqwYQGrNUO_BxUKatSsJL910iLPDHpSqQHYzP5ECbo1DiZQU-LokSt7au9U2v7ia2EWttPmU9H-FwP0L4ljnUnnR_03rz2v8wEauyXYLz1r4u6m619gd8xcd-Iamy7lPry71Ra4u_7fwAD9KGk
CitedBy_id crossref_primary_10_1523_JNEUROSCI_3659_12_2013
crossref_primary_10_1101_lm_7_3_124
crossref_primary_10_2983_035_029_0328
crossref_primary_10_3389_fphys_2021_809529
crossref_primary_10_7554_eLife_56962
crossref_primary_10_1016_j_jmb_2005_12_009
crossref_primary_10_3389_fnana_2020_00035
crossref_primary_10_1152_jn_2001_86_2_792
crossref_primary_10_1152_jn_1999_82_6_3378
crossref_primary_10_1556_ABiol_63_2012_Suppl_2_18
crossref_primary_10_1002_dneu_22071
crossref_primary_10_1007_BF03543036
crossref_primary_10_1016_j_jinorgbio_2005_01_013
crossref_primary_10_1016_j_neuroscience_2012_10_005
crossref_primary_10_1002_1097_0029_20000615_49_6_557__AID_JEMT6_3_0_CO_2_S
crossref_primary_10_1242_jeb_205_7_877
crossref_primary_10_1523_JNEUROSCI_18_14_05463_1998
crossref_primary_10_3389_fnbeh_2023_1221794
crossref_primary_10_1046_j_1460_9568_1999_00731_x
crossref_primary_10_2108_zsj_27_602
crossref_primary_10_1007_s11055_014_9909_2
crossref_primary_10_2108_zs160136
crossref_primary_10_1007_s00359_010_0541_5
crossref_primary_10_1046_j_1460_9568_1999_00472_x
crossref_primary_10_1242_jeb_032227
crossref_primary_10_3389_fnmol_2021_670303
crossref_primary_10_1186_1742_9994_9_9
crossref_primary_10_1002_cne_21585
crossref_primary_10_1523_JNEUROSCI_21_08_02903_2001
crossref_primary_10_1002_1097_0029_20000615_49_6_534__AID_JEMT4_3_0_CO_2_6
crossref_primary_10_1523_JNEUROSCI_19_21_09618_1999
Cites_doi 10.1523/JNEUROSCI.16-16-04949.1996
10.1523/JNEUROSCI.14-07-04412.1994
10.1098/rstb.1992.0054
10.1152/jn.1988.59.5.1613
10.1098/rstb.1992.0053
10.1016/0169-328X(94)90172-4
10.1523/JNEUROSCI.14-11-06564.1994
10.1016/S0021-9258(18)43810-0
10.1016/0006-8993(88)91325-X
10.1152/jn.1993.70.1.37
10.1016/0306-4492(81)90007-1
10.1002/cne.903140402
10.1002/cne.903420303
10.1152/jn.1995.73.1.112
10.1016/B978-0-12-185267-2.50010-6
10.1210/endo.134.4.8137747
10.1007/BF01928164
10.1152/jn.1994.72.3.1357
10.1046/j.1471-4159.1996.66010321.x
10.1002/cne.903420304
10.1242/jeb.85.1.149
10.1523/JNEUROSCI.14-07-04393.1994
10.1523/JNEUROSCI.13-06-02719.1993
10.1152/jn.1995.74.1.54
10.1073/pnas.84.15.5483
10.1242/jeb.80.1.119
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7TK
F1W
H95
L.G
7X8
DOI 10.1152/jn.1998.79.5.2460
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
Neurosciences Abstracts
ASFA: Aquatic Sciences and Fisheries Abstracts
Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources
Aquatic Science & Fisheries Abstracts (ASFA) Professional
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
Aquatic Science & Fisheries Abstracts (ASFA) Professional
Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources
Neurosciences Abstracts
ASFA: Aquatic Sciences and Fisheries Abstracts
MEDLINE - Academic
DatabaseTitleList
CrossRef
MEDLINE - Academic
Aquatic Science & Fisheries Abstracts (ASFA) Professional
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
EISSN 1522-1598
EndPage 2474
ExternalDocumentID 10_1152_jn_1998_79_5_2460
9582220
jn_79_5_2460
Genre Research Support, Non-U.S. Gov't
Journal Article
Comparative Study
GroupedDBID -
08R
0VX
1Z7
2WC
39C
3O-
41
53G
55
5GY
5VS
AALRV
ABFLS
ABIVO
ABPTK
ABUFD
ABZEH
ACGFS
ACNCT
ADACO
ADBBV
ADBIT
ADKLL
AENEX
AETEA
AFFNX
ALMA_UNASSIGNED_HOLDINGS
BAWUL
C1A
CS3
DIK
DL
DU5
DZ
E3Z
EBS
EJD
F5P
FH7
FRP
GJ
GX1
H~9
KQ8
L7B
MVM
NEJ
O0-
OHT
OK1
P2P
RAP
RHF
RHI
RPL
SJN
UHB
UPT
UQL
VH1
WH7
WOQ
WOW
X
X7M
ZA5
ZGI
ZXP
ZY4
---
-DZ
-~X
.55
.GJ
18M
1CY
29L
4.4
41~
476
8M5
ABCQX
ABJNI
ABKWE
ABTAH
ACGFO
ADFNX
ADIYS
AFOSN
AI.
AIZAD
BKKCC
BTFSW
CGR
CUY
CVF
ECM
EIF
EMOBN
H13
ITBOX
NPM
RPRKH
TR2
W8F
XJT
XOL
XSW
YBH
YQT
YSK
AAYXX
CITATION
7TK
F1W
H95
L.G
7X8
ID FETCH-LOGICAL-c403t-a8d5cc395a95936602131300269654518ea9b9b2a8c58e5ed0e4354fb8226b443
ISSN 0022-3077
IngestDate Fri Oct 25 22:14:00 EDT 2024
Fri Oct 25 23:56:01 EDT 2024
Thu Sep 26 17:40:49 EDT 2024
Sat Sep 28 08:46:05 EDT 2024
Mon May 06 12:28:25 EDT 2019
Tue Jan 05 17:56:55 EST 2021
IsPeerReviewed true
IsScholarly true
Issue 5
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c403t-a8d5cc395a95936602131300269654518ea9b9b2a8c58e5ed0e4354fb8226b443
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 9582220
PQID 16482214
PQPubID 23462
PageCount 15
ParticipantIDs proquest_miscellaneous_16482214
pubmed_primary_9582220
proquest_miscellaneous_79875272
highwire_physiology_jn_79_5_2460
crossref_primary_10_1152_jn_1998_79_5_2460
PublicationCentury 1900
PublicationDate 1998-05-01
PublicationDateYYYYMMDD 1998-05-01
PublicationDate_xml – month: 05
  year: 1998
  text: 1998-05-01
  day: 01
PublicationDecade 1990
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Journal of neurophysiology
PublicationTitleAlternate J Neurophysiol
PublicationYear 1998
Publisher Am Phys Soc
Publisher_xml – name: Am Phys Soc
References B21
B22
B23
B24
B25
B26
B27
Benjamin P. R. (B2) 1979; 80
B28
B29
B10
B11
B13
B14
McCrohan C. R. (B20) 1980; 85
B16
B17
Lloyd P. E. (B19) 1988; 19
B18
B1
B4
B5
B6
B7
B8
B9
Li K. W. (B15) 1994; 269
References_xml – ident: B13
  doi: 10.1523/JNEUROSCI.16-16-04949.1996
– ident: B6
  doi: 10.1523/JNEUROSCI.14-07-04412.1994
– ident: B10
  doi: 10.1098/rstb.1992.0054
– ident: B18
  doi: 10.1152/jn.1988.59.5.1613
– ident: B11
  doi: 10.1098/rstb.1992.0053
– ident: B17
  doi: 10.1016/0169-328X(94)90172-4
– ident: B14
  doi: 10.1523/JNEUROSCI.14-11-06564.1994
– volume: 269
  start-page: 30288
  year: 1994
  ident: B15
  publication-title: J. Biol. Chem.
  doi: 10.1016/S0021-9258(18)43810-0
  contributor:
    fullname: Li K. W.
– ident: B24
  doi: 10.1016/0006-8993(88)91325-X
– ident: B27
  doi: 10.1152/jn.1993.70.1.37
– ident: B1
  doi: 10.1016/0306-4492(81)90007-1
– ident: B21
  doi: 10.1002/cne.903140402
– volume: 19
  start-page: 55
  year: 1988
  ident: B19
  publication-title: J. Neurophysiol.
  contributor:
    fullname: Lloyd P. E.
– ident: B23
  doi: 10.1002/cne.903420303
– ident: B29
  doi: 10.1152/jn.1995.73.1.112
– ident: B8
  doi: 10.1016/B978-0-12-185267-2.50010-6
– ident: B16
  doi: 10.1210/endo.134.4.8137747
– ident: B26
  doi: 10.1007/BF01928164
– ident: B28
  doi: 10.1152/jn.1994.72.3.1357
– ident: B25
  doi: 10.1046/j.1471-4159.1996.66010321.x
– ident: B22
  doi: 10.1002/cne.903420304
– volume: 85
  start-page: 149
  year: 1980
  ident: B20
  publication-title: J. Exp. Biol.
  doi: 10.1242/jeb.85.1.149
  contributor:
    fullname: McCrohan C. R.
– ident: B5
  doi: 10.1523/JNEUROSCI.14-07-04393.1994
– ident: B7
  doi: 10.1523/JNEUROSCI.13-06-02719.1993
– ident: B4
  doi: 10.1152/jn.1995.74.1.54
– ident: B9
  doi: 10.1073/pnas.84.15.5483
– volume: 80
  start-page: 119
  year: 1979
  ident: B2
  publication-title: J. Exp. Biol.
  doi: 10.1242/jeb.80.1.119
  contributor:
    fullname: Benjamin P. R.
SSID ssj0007502
Score 1.753997
Snippet Stephen J. Perry 1 , Volko A. Straub 1 , György Kemenes 1 , Niovi Santama 1 , Belinda M. Worster 1 , Julian F. Burke 2 , and Paul R. Benjamin 1 1  Sussex...
Families of peptide neuromodulators are believed to play important roles in neural networks that control behaviors. Here, we investigate the expression and...
Perry, Stephen J., Volko A. Straub, György Kemenes, Niovi Santama, Belinda M. Worster, Julian F. Burke, and Paul R. Benjamin. Neural modulation of gut motility...
SourceID proquest
crossref
pubmed
highwire
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 2460
SubjectTerms Acetylcholine - pharmacology
Acetylcholine - physiology
Animals
Esophagus - drug effects
Esophagus - innervation
Esophagus - physiology
Freshwater
Gastrointestinal Motility - drug effects
Gastrointestinal Motility - physiology
Gene Expression
Immunoenzyme Techniques
In Situ Hybridization
Lymnaea
Lymnaea - drug effects
Lymnaea - physiology
Motor Neurons - chemistry
Motor Neurons - drug effects
Motor Neurons - physiology
Neuropeptides - biosynthesis
Neuropeptides - genetics
Neuropeptides - pharmacology
Neuropeptides - physiology
Peptide Fragments - pharmacology
RNA, Messenger - analysis
Title Neural Modulation of Gut Motility by Myomodulin Peptides and Acetylcholine in the Snail Lymnaea
URI http://jn.physiology.org/cgi/content/abstract/79/5/2460
https://www.ncbi.nlm.nih.gov/pubmed/9582220
https://search.proquest.com/docview/16482214
https://search.proquest.com/docview/79875272
Volume 79
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3Pb9MwFLZgXLggYEwUGPiAOFBS0sRO4uOENk1QxtBa1Jtlx860aUmmLj1kfz3Pzg-n2ip-XKIqdZzG39eXz35-7yH03uQAVyrLPJYBDMRPQ08qLT2tmB8IEaRJZjy630-i4wX5uqRLV-7IRpdUcpLe3htX8j-owjnA1UTJ_gOyfadwAj4DvnAEhOH4VxibzBom-qNUbREuI_3O19XY7LCz-hrEZV6XtoHdLg4GQukmLbNIdVVfGet30WQOMRL0phAXV-NZnRdCiy3C1abAtCsiG0vyp3rVuOTPBq6maiXW1uPzazyw7bluCwT0hb3OAGCRC-cbUi4yr9v2NwwM8NuqLK1xbSrFtCSiQ0tJmjoC7Vs3IE2xnrsWnZoMsZeFCatMJjGb0Im7dJg9--QHP1rMZnx-uJw_RI8CMDzG4n376bLHgzpy2ePhh7ZebrjF5zs32NQpXe7o7fMQq0fmT9GTFg980LDiGXqgi-do96AQVZnX-AM-7QHaRbwhCnZEwWWGgSi4IwqWNXZEwR1RMBAFbxAFw7dAFGyJgluivECLo8P5l2OvrazhpcQPK08kiqZpyKgweamjCIReaPyaQcQikNTTRAsmmQxEktJEU618DbKaZBLkZCQJCffQTlEW-iXCkvhap0xGNFYE9LwgvkhEJOPMT4iY0hH62I0jv24SqHA78aQBvyy4GXQeM065GfQR-tSNNHc85mY1Zg5gwwV9U36tshHC9zWHbgc9vusA42A4jTdMFLpc3_BpROBppmR7i5jBZD6IgxHaa5DuH4BRo6v9V3_s_DV67P4qb9BOtVrrfVCxlXxrqfkbVt2gxA
link.rule.ids 315,783,787,27936,27937
linkProvider Colorado Alliance of Research Libraries
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Neural+modulation+of+gut+motility+by+myomodulin+peptides+and+acetylcholine+in+the+snail+Lymnaea&rft.jtitle=Journal+of+neurophysiology&rft.au=Perry%2C+S+J&rft.au=Straub%2C+V+A&rft.au=Kemenes%2C+G&rft.au=Santama%2C+N&rft.date=1998-05-01&rft.issn=0022-3077&rft.volume=79&rft.issue=5&rft.spage=2460&rft.epage=2474&rft_id=info:doi/10.1152%2Fjn.1998.79.5.2460&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0022-3077&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0022-3077&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0022-3077&client=summon