MS14, a marine herbal medicine, an immunosuppressive drug in experimental autoimmune encephalomyelitis

Background : Cytokines are secreted signaling proteins which play essential roles in immune responses during experimental autoimmune encephalomyelitis (EAE), a demyelinating model that mimics many features of multiple sclerosis (MS). Interleukin 6 (IL-6) is a multifunctional cytokine produced by dif...

Full description

Saved in:
Bibliographic Details
Published inIranian red crescent medical journal Vol. 16; no. 7; pp. 1 - 6
Main Authors Kalan, Abbas Ibrahimi, Khaki, Amir Afshin, Rawshandah, Amanh Muhammadi, Rad, Jafar Sulaymani, Kafami, Laya, Muhammadnezhad, Daryoush
Format Journal Article
LanguageEnglish
Published Dubai, United Arab Emirates Iranian Hospital 01.07.2014
Zamen Salamati Publishing
Kowsar
Subjects
Online AccessGet full text
ISSN2074-1804
2074-1812
DOI10.5812/ircmj.16956

Cover

Loading…
Abstract Background : Cytokines are secreted signaling proteins which play essential roles in immune responses during experimental autoimmune encephalomyelitis (EAE), a demyelinating model that mimics many features of multiple sclerosis (MS). Interleukin 6 (IL-6) is a multifunctional cytokine produced by different cells, mediating inflammatory reactions and immune-mediated processes. Several studies have described immunosuppressive potentials of several herbal medicines. MS14 as an Iranian marine herbal medicine has anti-inflammatory and immunomodulatory activities. Objectives : The present study investigated the immunosuppressive potential of MS14 as an herbal drug as well as the IL-6 level in EAE model. We hope it will be a new approach for neurologic diseases and autoimmune originated diseases therapy. Patients and Methods : The present experimental study was a collaboration between Department of Anatomical Sciences of Tabriz University of Medical Sciences and Shefa Neuroscience Research Center of Tehran. We used 30 C57BL/6 mice. The animals were immunized with myelin oligodendrocyte glycoprotein (MOG) to induce EAE and treated with MS14-containing (30 %) diets. Subjects were selected by simple random sampling and then they were randomly allocated to two groups. EAE symptoms were assessed using the standard 10–point EAE scoring system from the seventh to the 35th day after immunization. Afterwards, the spleen was removed and its cells were cultured with or without MOG 35-55 ; then, the IL-6 level was analyzed by ELISA. In addition, histopathological studies were carried out for demyelination lesion evaluation in the spinal cord. Results : MS14 significantly improved clinical symptoms of EAE compared with the control (P < 0.05). It also suppressed proliferative responses of T cells and decreased IL-6 expression (16.93 ± 2.7 vs. 21.4 ± 3.33) (P < 0.05). Conclusions : Our results strongly suggested that IL-6 as a potential molecule could have a role in neuroimmunology and neuroinflammation, which is in congruent with previous studies. Therefore, it can be a clear target in strategic therapies and support effective properties of phytotherapy in EAE and MS treatment.
AbstractList Cytokines are secreted signaling proteins which play essential roles in immune responses during experimental autoimmune encephalomyelitis (EAE), a demyelinating model that mimics many features of multiple sclerosis (MS). Interleukin 6 (IL-6) is a multifunctional cytokine produced by different cells, mediating inflammatory reactions and immune-mediated processes. Several studies have described immunosuppressive potentials of several herbal medicines. MS14 as an Iranian marine herbal medicine has anti-inflammatory and immunomodulatory activities. The present study investigated the immunosuppressive potential of MS14 as an herbal drug as well as the IL-6 level in EAE model. We hope it will be a new approach for neurologic diseases and autoimmune originated diseases therapy. The present experimental study was a collaboration between Department of Anatomical Sciences of Tabriz University of Medical Sciences and Shefa Neuroscience Research Center of Tehran. We used 30 C57BL/6 mice. The animals were immunized with myelin oligodendrocyte glycoprotein (MOG) to induce EAE and treated with MS14-containing (30%) diets. Subjects were selected by simple random sampling and then they were randomly allocated to two groups. EAE symptoms were assessed using the standard 10-point EAE scoring system from the seventh to the 35th day after immunization. Afterwards, the spleen was removed and its cells were cultured with or without MOG 35-55; then, the IL-6 level was analyzed by ELISA. In addition, histopathological studies were carried out for demyelination lesion evaluation in the spinal cord. MS14 significantly improved clinical symptoms of EAE compared with the control (P < 0.05). It also suppressed proliferative responses of T cells and decreased IL-6 expression (16.93 ± 2.7 vs. 21.4 ± 3.33) (P < 0.05). Our results strongly suggested that IL-6 as a potential molecule could have a role in neuroimmunology and neuroinflammation, which is in congruent with previous studies. Therefore, it can be a clear target in strategic therapies and support effective properties of phytotherapy in EAE and MS treatment.
Cytokines are secreted signaling proteins which play essential roles in immune responses during experimental autoimmune encephalomyelitis (EAE), a demyelinating model that mimics many features of multiple sclerosis (MS). Interleukin 6 (IL-6) is a multifunctional cytokine produced by different cells, mediating inflammatory reactions and immune-mediated processes. Several studies have described immunosuppressive potentials of several herbal medicines. MS14 as an Iranian marine herbal medicine has anti-inflammatory and immunomodulatory activities.BACKGROUNDCytokines are secreted signaling proteins which play essential roles in immune responses during experimental autoimmune encephalomyelitis (EAE), a demyelinating model that mimics many features of multiple sclerosis (MS). Interleukin 6 (IL-6) is a multifunctional cytokine produced by different cells, mediating inflammatory reactions and immune-mediated processes. Several studies have described immunosuppressive potentials of several herbal medicines. MS14 as an Iranian marine herbal medicine has anti-inflammatory and immunomodulatory activities.The present study investigated the immunosuppressive potential of MS14 as an herbal drug as well as the IL-6 level in EAE model. We hope it will be a new approach for neurologic diseases and autoimmune originated diseases therapy.OBJECTIVESThe present study investigated the immunosuppressive potential of MS14 as an herbal drug as well as the IL-6 level in EAE model. We hope it will be a new approach for neurologic diseases and autoimmune originated diseases therapy.The present experimental study was a collaboration between Department of Anatomical Sciences of Tabriz University of Medical Sciences and Shefa Neuroscience Research Center of Tehran. We used 30 C57BL/6 mice. The animals were immunized with myelin oligodendrocyte glycoprotein (MOG) to induce EAE and treated with MS14-containing (30%) diets. Subjects were selected by simple random sampling and then they were randomly allocated to two groups. EAE symptoms were assessed using the standard 10-point EAE scoring system from the seventh to the 35th day after immunization. Afterwards, the spleen was removed and its cells were cultured with or without MOG 35-55; then, the IL-6 level was analyzed by ELISA. In addition, histopathological studies were carried out for demyelination lesion evaluation in the spinal cord.PATIENTS AND METHODSThe present experimental study was a collaboration between Department of Anatomical Sciences of Tabriz University of Medical Sciences and Shefa Neuroscience Research Center of Tehran. We used 30 C57BL/6 mice. The animals were immunized with myelin oligodendrocyte glycoprotein (MOG) to induce EAE and treated with MS14-containing (30%) diets. Subjects were selected by simple random sampling and then they were randomly allocated to two groups. EAE symptoms were assessed using the standard 10-point EAE scoring system from the seventh to the 35th day after immunization. Afterwards, the spleen was removed and its cells were cultured with or without MOG 35-55; then, the IL-6 level was analyzed by ELISA. In addition, histopathological studies were carried out for demyelination lesion evaluation in the spinal cord.MS14 significantly improved clinical symptoms of EAE compared with the control (P < 0.05). It also suppressed proliferative responses of T cells and decreased IL-6 expression (16.93 ± 2.7 vs. 21.4 ± 3.33) (P < 0.05).RESULTSMS14 significantly improved clinical symptoms of EAE compared with the control (P < 0.05). It also suppressed proliferative responses of T cells and decreased IL-6 expression (16.93 ± 2.7 vs. 21.4 ± 3.33) (P < 0.05).Our results strongly suggested that IL-6 as a potential molecule could have a role in neuroimmunology and neuroinflammation, which is in congruent with previous studies. Therefore, it can be a clear target in strategic therapies and support effective properties of phytotherapy in EAE and MS treatment.CONCLUSIONSOur results strongly suggested that IL-6 as a potential molecule could have a role in neuroimmunology and neuroinflammation, which is in congruent with previous studies. Therefore, it can be a clear target in strategic therapies and support effective properties of phytotherapy in EAE and MS treatment.
Background : Cytokines are secreted signaling proteins which play essential roles in immune responses during experimental autoimmune encephalomyelitis (EAE), a demyelinating model that mimics many features of multiple sclerosis (MS). Interleukin 6 (IL-6) is a multifunctional cytokine produced by different cells, mediating inflammatory reactions and immune-mediated processes. Several studies have described immunosuppressive potentials of several herbal medicines. MS14 as an Iranian marine herbal medicine has anti-inflammatory and immunomodulatory activities. Objectives : The present study investigated the immunosuppressive potential of MS14 as an herbal drug as well as the IL-6 level in EAE model. We hope it will be a new approach for neurologic diseases and autoimmune originated diseases therapy. Patients and Methods : The present experimental study was a collaboration between Department of Anatomical Sciences of Tabriz University of Medical Sciences and Shefa Neuroscience Research Center of Tehran. We used 30 C57BL/6 mice. The animals were immunized with myelin oligodendrocyte glycoprotein (MOG) to induce EAE and treated with MS14-containing (30 %) diets. Subjects were selected by simple random sampling and then they were randomly allocated to two groups. EAE symptoms were assessed using the standard 10–point EAE scoring system from the seventh to the 35th day after immunization. Afterwards, the spleen was removed and its cells were cultured with or without MOG 35-55 ; then, the IL-6 level was analyzed by ELISA. In addition, histopathological studies were carried out for demyelination lesion evaluation in the spinal cord. Results : MS14 significantly improved clinical symptoms of EAE compared with the control (P < 0.05). It also suppressed proliferative responses of T cells and decreased IL-6 expression (16.93 ± 2.7 vs. 21.4 ± 3.33) (P < 0.05). Conclusions : Our results strongly suggested that IL-6 as a potential molecule could have a role in neuroimmunology and neuroinflammation, which is in congruent with previous studies. Therefore, it can be a clear target in strategic therapies and support effective properties of phytotherapy in EAE and MS treatment.
Author Kafami, Laya
Khaki, Amir Afshin
Kalan, Abbas Ibrahimi
Rad, Jafar Sulaymani
Rawshandah, Amanh Muhammadi
Muhammadnezhad, Daryoush
AuthorAffiliation 4 Anatomical Sciences Department, School of Medicine, Hamedan University of Medical Sciences, Hamedan, IR Iran
3 Pathobiology Department, School of Medicine, Alborz University of Medical Sciences, Karaj, IR Iran
1 Anatomical Sciences Department, School of Medicine, Tabriz University of Medical Sciences, Tabriz, IR Iran
2 Shefa Neuroscience Research Center, Tehran, IR Iran
AuthorAffiliation_xml – name: 3 Pathobiology Department, School of Medicine, Alborz University of Medical Sciences, Karaj, IR Iran
– name: 1 Anatomical Sciences Department, School of Medicine, Tabriz University of Medical Sciences, Tabriz, IR Iran
– name: 2 Shefa Neuroscience Research Center, Tehran, IR Iran
– name: 4 Anatomical Sciences Department, School of Medicine, Hamedan University of Medical Sciences, Hamedan, IR Iran
Author_xml – sequence: 1
  fullname: Kalan, Abbas Ibrahimi
– sequence: 2
  fullname: Khaki, Amir Afshin
– sequence: 3
  fullname: Rawshandah, Amanh Muhammadi
– sequence: 4
  fullname: Rad, Jafar Sulaymani
– sequence: 5
  fullname: Kafami, Laya
– sequence: 6
  fullname: Muhammadnezhad, Daryoush
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25237574$$D View this record in MEDLINE/PubMed
BookMark eNptkUtv1DAUhS1URB-wYg2KxAYJpvgdZ1MJVbykIhbA2nLs645HiR3spKL_Hs9MO4KKjV_3u8fn6pyio5giIPSc4HOhCH0Xsh0350R2Qj5CJxS3fEXq-9HhjPkxOi1lg7HoJGVP0DEVlLWi5SfIf_1O-NvGNKPJIUKzhtyboRnBBVvvtRKbMI5LTGWZpgylhBtoXF6umxAb-D1BDiPEufaYZU47FBqIFqa1GdJ4C0OYQ3mKHnszFHh2t5-hnx8__Lj8vLr69unL5furlWVcypXnmHnnhagLdd61rvfSOyW9MkowykjXkb7FUlLHOQPBuOtx6ymjylrXsTN0sdedlr7OYKuzbAY9VZMm3-pkgv63EsNaX6cbzYmUuGNV4PWdQE6_FiizHkOxMAwmQlqKJkKyThElt3-9eoBu0pJjHa9SvBOCKK4q9fJvRwcr9xFUgOwBm1MpGby2YTZzSFuDYdAE623Mehez3sVce9486LmX_T_9Yk9DRcCbA8xUK-ogfwDkLrWu
CitedBy_id crossref_primary_10_1186_s12906_024_04587_y
crossref_primary_10_15171_apb_2018_066
crossref_primary_10_1515_revneuro_2018_0057
crossref_primary_10_1007_s12031_016_0834_4
Cites_doi 10.1038/nprot.2006.285
10.1016/j.humimm.2008.07.014
10.1038/324073a0
10.3109/00207454.2013.764499
10.1007/s11655-010-0270-1
10.3109/08923973.2010.543687
10.1016/j.jss.2009.03.026
10.1007/s00415-004-0348-9
10.1002/(SICI)1097-0142(20000501)88:9<2061::AID-CNCR12>3.0.CO;2-O
10.1007/s00415-010-5689-y
10.1016/j.jneuroim.2012.04.015
10.1111/j.1440-1746.1994.tb01275.x
10.1097/00019052-200206000-00001
10.4049/jimmunol.173.9.5794
10.1002/ana.20913
10.1172/JCI15751
10.7150/ijbs.4679
10.2165/11313470-000000000-00000
10.1111/j.1365-2567.2005.02200.x
10.4049/jimmunol.1103721
10.1016/S0165-5728(99)00187-3
10.1016/S0304-3940(00)01543-3
10.1016/j.jocn.2012.12.022
10.1016/j.jneuroim.2012.10.015
10.1038/ni1488
10.4049/jimmunol.1202925
10.1002/ptr.2459
ContentType Journal Article
Contributor Kafami, Laya
Khaki, Amir Afshin
Kalan, Abbas Ibrahimi
Rad, Jafar Sulaymani
Rawshandah, Amanh Muhammadi
Muhammadnezhad, Daryoush
Contributor_xml – sequence: 1
  fullname: Kalan, Abbas Ibrahimi
– sequence: 2
  fullname: Khaki, Amir Afshin
– sequence: 3
  fullname: Rawshandah, Amanh Muhammadi
– sequence: 4
  fullname: Rad, Jafar Sulaymani
– sequence: 5
  fullname: Kafami, Laya
– sequence: 6
  fullname: Muhammadnezhad, Daryoush
Copyright Copyright Iranian Hospital Dubai Jul 2014
Copyright © 2014, Iranian Red Crescent Medical Journal; Published by Kowsar Corp. 2014
Copyright_xml – notice: Copyright Iranian Hospital Dubai Jul 2014
– notice: Copyright © 2014, Iranian Red Crescent Medical Journal; Published by Kowsar Corp. 2014
DBID AACQA
ADJCN
AEION
AHFXO
AHHHR
AAYXX
CITATION
NPM
3V.
7X7
7XB
8FI
8FJ
8FK
8G5
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
CWDGH
DWQXO
FYUFA
GHDGH
GNUQQ
GUQSH
K9.
M0S
M2O
MBDVC
PHGZM
PHGZT
PKEHL
PQEST
PQQKQ
PQUKI
Q9U
7X8
5PM
DOI 10.5812/ircmj.16956
DatabaseName بنك معلومات "معرفة" لدراسات العلوم العسكرية والأمنية - e-Marefa Military & Security Database
الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals
مجلس التعاون الخليجي وإيران - e-Marefa The GCC-Iranian Affairs
معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete
دراسات الشرق الأوسط - e-Marefa Middle Eastern Studies
CrossRef
PubMed
ProQuest Central (Corporate)
Health & Medical Collection (ProQuest)
ProQuest Central (purchase pre-March 2016)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Research Library
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
ProQuest One
Middle East & Africa Database
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
ProQuest Research Library
ProQuest Health & Medical Complete (Alumni)
Health & Medical Collection (Alumni)
Research Library (ProQuest)
Research Library (Corporate)
ProQuest Central Premium
ProQuest One Academic (New)
ProQuest One Academic Middle East (New)
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central Basic
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
PubMed
Research Library Prep
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
Research Library (Alumni Edition)
ProQuest Central
Health Research Premium Collection
Middle East & Africa Database
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
ProQuest Research Library
ProQuest Central (New)
ProQuest Central Basic
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList PubMed
MEDLINE - Academic

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: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2074-1812
EndPage 6
ExternalDocumentID PMC4166093
3388089351
25237574
10_5812_ircmj_16956
387569
Genre Journal Article
General Information
GroupedDBID 29J
3V.
53G
5GY
7X7
8FI
8FJ
8G5
AACQA
ABUWG
ADBBV
ADJCN
ADRAZ
AEION
AENEX
AFKRA
AHFXO
AHHHR
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AZQEC
BAWUL
BENPR
BPHCQ
BVXVI
CCPQU
CWDGH
DIK
DWQXO
E3Z
FYUFA
GNUQQ
GUQSH
HMCUK
HYE
KQ8
M2O
M48
M~E
OK1
PGMZT
PQQKQ
PROAC
RNS
RPM
TR2
UKHRP
AAYXX
CITATION
PHGZM
PHGZT
NPM
7XB
8FK
K9.
MBDVC
PKEHL
PQEST
PQUKI
Q9U
7X8
5PM
ID FETCH-LOGICAL-c3466-f403fdf55fdf2dfd7dbf6fd86f8a853231991b70662d443e534db07f2328ccd93
IEDL.DBID 7X7
ISSN 2074-1804
IngestDate Thu Aug 21 13:57:49 EDT 2025
Fri Jul 11 03:35:16 EDT 2025
Sun Jun 29 15:53:50 EDT 2025
Thu Apr 03 07:03:24 EDT 2025
Tue Jul 01 01:31:02 EDT 2025
Thu Apr 24 22:52:11 EDT 2025
Tue Nov 26 17:08:06 EST 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed false
IsScholarly true
Issue 7
Keywords EAE
Herbal Medicine
Interleukin-6
LCCallNum_Ident RM
Language English
License This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3466-f403fdf55fdf2dfd7dbf6fd86f8a853231991b70662d443e534db07f2328ccd93
Notes SourceType-Scholarly Journals-1
ObjectType-General Information-1
content type line 14
ObjectType-Article-1
ObjectType-Feature-2
content type line 23
OpenAccessLink http://journals.scholarsportal.info/openUrl.xqy?doi=10.5812/ircmj.16956
PMID 25237574
PQID 1549551848
PQPubID 105757
PageCount 6
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_4166093
proquest_miscellaneous_1563981869
proquest_journals_1549551848
pubmed_primary_25237574
crossref_citationtrail_10_5812_ircmj_16956
crossref_primary_10_5812_ircmj_16956
emarefa_primary_387569
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20140701
PublicationDateYYYYMMDD 2014-07-01
PublicationDate_xml – month: 7
  year: 2014
  text: 20140701
  day: 1
PublicationDecade 2010
PublicationPlace Dubai, United Arab Emirates
PublicationPlace_xml – name: Dubai, United Arab Emirates
– name: Iran
– name: Mashhad
PublicationTitle Iranian red crescent medical journal
PublicationTitleAlternate Iran Red Crescent Med J
PublicationYear 2014
Publisher Iranian Hospital
Zamen Salamati Publishing
Kowsar
Publisher_xml – name: Iranian Hospital
– name: Zamen Salamati Publishing
– name: Kowsar
References Van Wagoner NJ (key-A16956R13-13) 1999; 100
key-A16956R1-1
key-A16956R2-2
key-A16956R22-22
key-A16956R24-24
key-A16956R28-28
key-A16956R4-4
key-A16956R26-26
key-A16956R6-6
key-A16956R7-7
key-A16956R8-8
key-A16956R9-9
key-A16956R15-15
Hemmer B (key-A16956R3-3) 2002; 15
key-A16956R19-19
Mohyeddin Bonab M (key-A16956R20-20) 2007; 4
Aktas O (key-A16956R29-29) 2004; 173
key-A16956R30-30
Naseri M (key-A16956R17-17) 2007; 14
Rodgers JM (key-A16956R5-5) 2012; 85
key-A16956R23-23
key-A16956R21-21
key-A16956R27-27
key-A16956R25-25
Karczewska A (key-A16956R10-10) 2000; 88
Roya Y (key-A16956R16-16) 2011; 14
Okada K (key-A16956R11-11) 1994; 9
Schonrock LM (key-A16956R14-14) 2000; 294
key-A16956R18-18
key-A16956R12-12
key-A16956R31-31
23177720 - J Neuroimmunol. 2013 Feb 15;255(1-2):39-44
18723060 - Hum Immunol. 2008 Nov;69(11):797-804
17581537 - Nat Immunol. 2007 Sep;8(9):967-74
23916471 - J Clin Neurosci. 2014 Jan;21(1):12-21
23225885 - J Immunol. 2013 Jan 1;190(1):138-46
23239947 - Yale J Biol Med. 2012 Dec;85(4):447-68
11044583 - Neurosci Lett. 2000 Nov 10;294(1):45-8
19712003 - Mol Diagn Ther. 2009;13(4):225-44
17652844 - Iran J Immunol. 2007 Mar;4(1):50-7
12045717 - Curr Opin Neurol. 2002 Jun;15(3):227-31
23267024 - J Immunol. 2013 Feb 1;190(3):881-5
16011525 - Immunology. 2005 Aug;115(4):565-74
10813718 - Cancer. 2000 May 1;88(9):2061-71
23136554 - Int J Biol Sci. 2012;8(9):1254-66
10695723 - J Neuroimmunol. 1999 Dec;100(1-2):124-39
17487163 - Nat Protoc. 2006;1(4):1810-9
20689961 - J Neurol. 2010 Sep;257(9):1590-3
21284543 - Immunopharmacol Immunotoxicol. 2011 Sep;33(3):509-14
16802293 - Ann Neurol. 2006 Jul;60(1):12-21
22633195 - J Neuroimmunol. 2012 Aug 15;249(1-2):109-11
12189243 - J Clin Invest. 2002 Aug;110(4):493-7
15015004 - J Neurol. 2004 Mar;251(3):261-8
15494532 - J Immunol. 2004 Nov 1;173(9):5794-800
3491322 - Nature. 1986 Nov 6-12;324(6092):73-6
23301896 - Int J Neurosci. 2013 Jul;123(7):480-6
18570265 - Phytother Res. 2008 Aug;22(8):1083-6
7827297 - J Gastroenterol Hepatol. 1994 Sep-Oct;9(5):462-7
19555978 - J Surg Res. 2010 Jul;162(1):54-8
20694784 - Chin J Integr Med. 2010 Jun;16(3):270-1
References_xml – ident: key-A16956R22-22
  doi: 10.1038/nprot.2006.285
– ident: key-A16956R4-4
  doi: 10.1016/j.humimm.2008.07.014
– volume: 14
  start-page: 64
  issue: 68
  year: 2007
  ident: key-A16956R17-17
  publication-title: Daneshvar Med.
– ident: key-A16956R9-9
  doi: 10.1038/324073a0
– ident: key-A16956R31-31
  doi: 10.3109/00207454.2013.764499
– ident: key-A16956R18-18
  doi: 10.1007/s11655-010-0270-1
– ident: key-A16956R30-30
  doi: 10.3109/08923973.2010.543687
– ident: key-A16956R12-12
  doi: 10.1016/j.jss.2009.03.026
– ident: key-A16956R15-15
  doi: 10.1007/s00415-004-0348-9
– volume: 88
  start-page: 2061
  issue: 9
  year: 2000
  ident: key-A16956R10-10
  publication-title: Cancer.
  doi: 10.1002/(SICI)1097-0142(20000501)88:9<2061::AID-CNCR12>3.0.CO;2-O
– volume: 4
  start-page: 50
  issue: 1
  year: 2007
  ident: key-A16956R20-20
  publication-title: Iran J Immunol.
– volume: 14
  start-page: 89
  issue: 1
  year: 2011
  ident: key-A16956R16-16
  publication-title: Iran J Basic Med Sci.
– ident: key-A16956R7-7
  doi: 10.1007/s00415-010-5689-y
– ident: key-A16956R1-1
  doi: 10.1016/j.jneuroim.2012.04.015
– volume: 9
  start-page: 462
  issue: 5
  year: 1994
  ident: key-A16956R11-11
  publication-title: J Gastroenterol Hepatol.
  doi: 10.1111/j.1440-1746.1994.tb01275.x
– volume: 15
  start-page: 227
  issue: 3
  year: 2002
  ident: key-A16956R3-3
  publication-title: Curr Opin Neurol.
  doi: 10.1097/00019052-200206000-00001
– volume: 173
  start-page: 5794
  issue: 9
  year: 2004
  ident: key-A16956R29-29
  publication-title: J Immunol.
  doi: 10.4049/jimmunol.173.9.5794
– ident: key-A16956R2-2
  doi: 10.1002/ana.20913
– ident: key-A16956R23-23
  doi: 10.1172/JCI15751
– ident: key-A16956R24-24
  doi: 10.7150/ijbs.4679
– ident: key-A16956R28-28
  doi: 10.2165/11313470-000000000-00000
– ident: key-A16956R21-21
  doi: 10.1111/j.1365-2567.2005.02200.x
– ident: key-A16956R8-8
  doi: 10.4049/jimmunol.1103721
– volume: 85
  start-page: 447
  issue: 4
  year: 2012
  ident: key-A16956R5-5
  publication-title: Yale J Biol Med.
– volume: 100
  start-page: 124
  issue: 1-2
  year: 1999
  ident: key-A16956R13-13
  publication-title: J Neuroimmunol.
  doi: 10.1016/S0165-5728(99)00187-3
– volume: 294
  start-page: 45
  issue: 1
  year: 2000
  ident: key-A16956R14-14
  publication-title: Neurosci Lett.
  doi: 10.1016/S0304-3940(00)01543-3
– ident: key-A16956R25-25
  doi: 10.1016/j.jocn.2012.12.022
– ident: key-A16956R6-6
  doi: 10.1016/j.jneuroim.2012.10.015
– ident: key-A16956R27-27
  doi: 10.1038/ni1488
– ident: key-A16956R26-26
  doi: 10.4049/jimmunol.1202925
– ident: key-A16956R19-19
  doi: 10.1002/ptr.2459
– reference: 22633195 - J Neuroimmunol. 2012 Aug 15;249(1-2):109-11
– reference: 23301896 - Int J Neurosci. 2013 Jul;123(7):480-6
– reference: 18570265 - Phytother Res. 2008 Aug;22(8):1083-6
– reference: 23177720 - J Neuroimmunol. 2013 Feb 15;255(1-2):39-44
– reference: 23916471 - J Clin Neurosci. 2014 Jan;21(1):12-21
– reference: 20694784 - Chin J Integr Med. 2010 Jun;16(3):270-1
– reference: 23267024 - J Immunol. 2013 Feb 1;190(3):881-5
– reference: 16802293 - Ann Neurol. 2006 Jul;60(1):12-21
– reference: 10813718 - Cancer. 2000 May 1;88(9):2061-71
– reference: 15015004 - J Neurol. 2004 Mar;251(3):261-8
– reference: 17581537 - Nat Immunol. 2007 Sep;8(9):967-74
– reference: 17487163 - Nat Protoc. 2006;1(4):1810-9
– reference: 10695723 - J Neuroimmunol. 1999 Dec;100(1-2):124-39
– reference: 19712003 - Mol Diagn Ther. 2009;13(4):225-44
– reference: 16011525 - Immunology. 2005 Aug;115(4):565-74
– reference: 23239947 - Yale J Biol Med. 2012 Dec;85(4):447-68
– reference: 3491322 - Nature. 1986 Nov 6-12;324(6092):73-6
– reference: 15494532 - J Immunol. 2004 Nov 1;173(9):5794-800
– reference: 19555978 - J Surg Res. 2010 Jul;162(1):54-8
– reference: 23225885 - J Immunol. 2013 Jan 1;190(1):138-46
– reference: 23136554 - Int J Biol Sci. 2012;8(9):1254-66
– reference: 12045717 - Curr Opin Neurol. 2002 Jun;15(3):227-31
– reference: 7827297 - J Gastroenterol Hepatol. 1994 Sep-Oct;9(5):462-7
– reference: 11044583 - Neurosci Lett. 2000 Nov 10;294(1):45-8
– reference: 20689961 - J Neurol. 2010 Sep;257(9):1590-3
– reference: 21284543 - Immunopharmacol Immunotoxicol. 2011 Sep;33(3):509-14
– reference: 18723060 - Hum Immunol. 2008 Nov;69(11):797-804
– reference: 17652844 - Iran J Immunol. 2007 Mar;4(1):50-7
– reference: 12189243 - J Clin Invest. 2002 Aug;110(4):493-7
SSID ssj0059623
Score 1.9661022
Snippet Background : Cytokines are secreted signaling proteins which play essential roles in immune responses during experimental autoimmune encephalomyelitis (EAE), a...
Cytokines are secreted signaling proteins which play essential roles in immune responses during experimental autoimmune encephalomyelitis (EAE), a...
SourceID pubmedcentral
proquest
pubmed
crossref
emarefa
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1
SubjectTerms Encephalomyelitis
Herbs
Interleukin-6
Pathophysiology
Therapeutic use
الأمراض
الجهاز العصبي المركزي
SummonAdditionalLinks – databaseName: Scholars Portal Journals: Open Access
  dbid: M48
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1La9tAEB7SlJZeSl9p3SZlCzmVKrW0D0mnEhIHt6BeWkNuQvtKDLaU2lZp_n1n9CIOJpdFsKNFmtllvmVmvgE4jlQRKilNIFXqAmFxSENtAmOi0FiHDtNQ7XD2U01n4selvNyDvhlnp8D1zqsd9ZOarRYn__7cfsMDj_j1RKJ_-jpfmSUeeYVQ_xE8RpcU0wnNxBBOoA4zFGqOKPkwTMaiLdS7__KWa3rilgU-FLuQ5_0Eyjse6eIFPO-gJDttbf8S9lz5Cp5mXbD8NfjsVyi-sIJlBZX4sSlqEOV7AZwp2XcqD6nW9U2bD_vXsfNVfcXmJZvcof5np_WmmpOoYxMqc7wuFtXy1lHq3PoNzC4mv8-mQddWITBcKBV4MebeeilxiKy3sdVeeZsonxTovBHwIWbUMVHDWyG4k1xYPY49Yq_EGJvyA9gvq9K9A8a150bZJhoruEbfn-rI21QiiEi1FCP43Gs0Nx3nOLW-WOR49yD1543680b9IzgehG9aqo3dYgedaQYpjpculY7gsLdU3u-jnBjoiHROJCP4NEzjEaK4SFG6qiYZhGnE7IdLvG0NOywd4UU9ljH-Sbxl8kGA6Lm3Z8r5dUPTjVBXjVP-_uHP-gDPEIOJNgP4EPY3q9odIc7Z6I_NHv4Pyzf-EQ
  priority: 102
  providerName: Scholars Portal
Title MS14, a marine herbal medicine, an immunosuppressive drug in experimental autoimmune encephalomyelitis
URI https://search.emarefa.net/detail/BIM-387569
https://www.ncbi.nlm.nih.gov/pubmed/25237574
https://www.proquest.com/docview/1549551848
https://www.proquest.com/docview/1563981869
https://pubmed.ncbi.nlm.nih.gov/PMC4166093
Volume 16
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3da9RAEF-0RfGl1I_q1Xqs0Ccx9JL9SPZJar1yCimiFu4tZL_ag15y3l0K_e-dSfbiVYovIWGHkMwkO7_dmfkNIceJLGMphImEVC7iFg4q1iYyJomNdeAwDdYO5xdycsm_TcU0bLitQlrlZk5sJ2pbG9wjP0EqMWQP49mnxe8Iu0ZhdDW00HhMdpG6DFO60mm_4MLGMhhhTjDnMM5GvKvPE-DTTmZLM4dpQirsXL3lkZ64eQkn5UOA89-8yS1HdL5P9gKCpKedyZ-TR656QZ7mIUb-kvj8Z8w_0pLmJVb20QkoDuQ3AjBS0a9YFVKvmkWXBnvr6Jdlc0VnFR1vMf7T02Zdz1DU0TFWN16XN_X8zmHG3OoVuTwf_zqbRKGbQmQYlzLyfMS89ULAIbHeplZ76W0mfVaCzwacB1BRp8gIbzlnTjBu9Sj1ALkyY6xiB2Snqiv3hlCmPTPStkFYzjS4fKUTb5UA7KC04APyYaPRwgSqcex4cVPAkgPVX7TqL1r1D8hxL7zoGDYeFjsIpumlGKy1pBqQo42livD_rYq_X8uAvO-H4c_BcEhZubpBGUBnSOgHt3jdGba_dQLr81Sk8CbpPZP3AsjKfX-kml237NyAcOVIscP_P9Zb8gygF-8Sf4_IznrZuHcAb9Z62H7DQ7L7eXzx_Qdc5TwbtrtQfwCOlP72
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwzV3JTtxAEG0hUJYLWQmTkKQjkUsUw9i92D7kgJghnoC5BBRuxu4ljMLYaGaciPxKfiUflypvGRDKDSkXy1KXLC-vq167q14RsunJ1JVCKEfI0DhcwyF0M-Uo5blKGwiYCmuH40MZHfNPJ-Jkifxqa2EwrbL1iZWj1oXCf-TbKCWG6mE8aDIo983lD1ifzT6MBvAx33re3vBoN3KaFgKOYlxKx_I-s9oKAQdPW-3rzEqrA2mDFAIVkBvgR5mPMuiac2YE4zrr-xZ4RqCURqUl8O8rsKoQMH1Wdr8MPkato8e-NbiB7WFKoxv0eV3-JyBkbo-nagJeSIbYGHsh4N0xkxRO0pv47PW0zIU4t_eA_G7fUJ3e8m2rnGdb6uc18cj_9BU-JKsNv6Y79YR4RJZM_pjcjZsMgifExp9d_p6mNE6x7pFGACuwbw1gJKcjrJkpZuVFnST83dDBtPxKxzkdLvRDoDvlvBijqaFDrP08S8-LyaXBfMLZU3J8K0-5RpbzIjfrhLLMMiV1tUXNWQaEKMw8q0MBzCrMBO-Rdy0gEtUIsWM_kPMEFmSInqRCT1Khp0c2O-OLWn_kZrO1BlmdFYOVqAx7ZKPFQtJ4p1nyFwg98qYbBr-Cm0VpbooSbYC7otwhXOJZjcvu0p7wmC98eBL_CmI7A9QsvzqSj88q7XLg_7Ifsuf_vq3X5F50FB8kB6PD_RfkPpBUXqdIb5Dl-bQ0L4EIzrNXzYSk5PS2AfwHwRNt-Q
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V1Lb9NAEF5Vqai48C4ECixSuSDcxPbu2j4gVDUJCSUVElT0ZryvNmpjhyQGlZ_GX-HPMOMXaVVx64GLZWlHlr3-PPOtd-YbQrY9kbiCc-VwERmHaThErlSOUp6rtIGAqbB2eHwghofs_RE_WiO_6loYTKusfWLhqHWm8B95B6XEUD2MhR1bpUV87A3ezr452EEKd1rrdholRPbN-Q9Yvi3ejHrwrl963qD_eW_oVB0GHOUzIRzLur7VlnM4eNrqQEsrrA6FDROIY8B9gD7JAFXSNWO-4T7TshtYoCGhUhqFmMD9r2NXJ9Yi63tfeu-GdRzAtja4v-1hxqMbdllZHcghonYmczUFJyUi7Ju9Eg9vmGkCJ8lVdPdy1uZKGBzcJr_rCSyzX0538qXcUT8vaUv-nzN8h9yq2DndLT-nu2TNpPfIxrjKP7hP7PiTy17ThI4TrJqkQwAl2NcGMJLSEVbcZIt8VqYYfze0N8-P6SSl_ZVuCnQ3X2YTNDW0j5WjJ8lZNj03mI24eEAOr-UpN0krzVLziFBfWl8JXWxwM18CnYqkZ3XEgZdFkrM2eVXjJVaVjDt2EzmLYTmH4IoLcMUFuNpkuzGeleolV5ttVsBrrHxYx4qoTbZqqMSVb1vEf3HSJi-aYfBKuNWUpCbL0QaYL4olwiUelrBtLu1xzw94AE8SXAB0Y4CK5xdH0slJoXwOqwfRjfzH_76t52QDgBt_GB3sPyE3geGyMr96i7SW89w8BRa5lM-qz5WSr9eN3z9hZ4XJ
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=MS14%2C+a+Marine+Herbal+Medicine%2C+an+Immunosuppressive+Drug+in+Experimental+Autoimmune+Encephalomyelitis&rft.jtitle=Iranian+red+crescent+medical+journal&rft.au=Kalan%2C+Abbas+Ebrahimi&rft.au=Rad%2C+Jafar+Soleimani&rft.au=Kafami%2C+Laya&rft.au=Mohamadnezhad%2C+Daryoush&rft.date=2014-07-01&rft.pub=Zamen+Salamati+Publishing&rft.issn=2074-1804&rft.eissn=2074-1812&rft.volume=16&rft.issue=7&rft.spage=1&rft_id=info:doi/10.5812%2Fircmj.16956&rft.externalDBID=HAS_PDF_LINK&rft.externalDocID=3388089351
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2074-1804&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2074-1804&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2074-1804&client=summon