-
Je něco špatně v tomto záznamu ?
Protective effect of Clostridium tyrobutyricum in acute dextran sodium sulphate-induced colitis: differential regulation of tumour necrosis factor-α and interleukin-18 in BALB/c and severe combined immunodeficiency mice
T. Hudcovic, J. Kolinska, J. Klepetar, R. Stepankova, T. Rezanka, D. Srutkova, M. Schwarzer, V. Erban, Z. Du, JM. Wells, T. Hrncir, H. Tlaskalova-Hogenova, H. Kozakova
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 1966 do Před 1 rokem
PubMed Central
od 1966 do Před 1 rokem
Medline Complete (EBSCOhost)
od 1966-01-01 do Před 1 rokem
Wiley Online Library (archiv)
od 1990-01-01 do 2012-12-31
- MeSH
- akutní nemoc MeSH
- antigeny CD11b biosyntéza genetika MeSH
- aplikace rektální MeSH
- bakteriální translokace MeSH
- butyráty metabolismus MeSH
- Clostridium tyrobutyricum fyziologie MeSH
- fosfoproteiny biosyntéza genetika MeSH
- imunokompetence MeSH
- interleukin-18 biosyntéza genetika MeSH
- kolon metabolismus mikrobiologie patologie MeSH
- mastné kyseliny metabolismus MeSH
- membránové proteiny biosyntéza genetika MeSH
- mucin 2 biosyntéza genetika MeSH
- muciny biosyntéza MeSH
- myši inbrední BALB C MeSH
- myši SCID MeSH
- myši MeSH
- organismy bez specifických patogenů MeSH
- probiotika terapeutické užití MeSH
- síran dextranu toxicita MeSH
- těžká kombinovaná imunodeficience genetika imunologie MeSH
- TNF-alfa biosyntéza genetika MeSH
- ulcerózní kolitida chemicky indukované genetika imunologie mikrobiologie patologie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
One of the promising approaches in the therapy of ulcerative colitis is administration of butyrate, an energy source for colonocytes, into the lumen of the colon. This study investigates the effect of butyrate producing bacterium Clostridium tyrobutyricum on dextran sodium sulphate (DSS)-induced colitis in mice. Immunocompetent BALB/c and immunodeficient severe combined immunodeficiency (SCID) mice reared in specific-pathogen-free (SPF) conditions were treated intrarectally with C. tyrobutyricum 1 week prior to the induction of DSS colitis and during oral DSS treatment. Administration of DSS without C. tyrobutyricum treatment led to an appearance of clinical symptoms - bleeding, rectal prolapses and colitis-induced increase in the antigen CD11b, a marker of infiltrating inflammatory cells in the lamina propria. The severity of colitis was similar in BALB/c and SCID mice as judged by the histological damage score and colon shortening after 7 days of DSS treatment. Both strains of mice also showed a similar reduction in tight junction (TJ) protein zonula occludens (ZO)-1 expression and of MUC-2 mucin depression. Highly elevated levels of cytokine tumour necrosis factor (TNF)-α in the colon of SCID mice and of interleukin (IL)-18 in BALB/c mice were observed. Intrarectal administration of C. tyrobutyricum prevented appearance of clinical symptoms of DSS-colitis, restored normal MUC-2 production, unaltered expression of TJ protein ZO-1 and decreased levels of TNF-α and IL-18 in the descending colon of SCID and BALB/c mice, respectively. Some of these features can be ascribed to the increased production of butyrate in the lumen of the colon and its role in protection of barrier functions and regulation of IL-18 expression.
Food Research Institute Prague Czech Republic
Host Microbe Interactomics Animal Sciences Wageningen University Wageningen The Netherlands
Institute of Microbiology of Academy of Sciences of Czech Republic v v i Prague Czech Republic
Institute of Microbiology of the Academy of Sciences of the Czech Republic v v i Prague
Institute of Physiology of the Academy of Sciences of the Czech Republic v v i Prague
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12022183
- 003
- CZ-PrNML
- 005
- 20160215093828.0
- 007
- ta
- 008
- 120806s2012 xxk f 000 0#eng||
- 009
- AR
- 024 7_
- $a 10.1111/j.1365-2249.2011.04498.x $2 doi
- 035 __
- $a (PubMed)22236013
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Hudcovic, Tomáš. $7 xx0267225 $u Institute of Microbiology of Academy of Sciences of Czech Republic, v.v.i., Prague, Czech Republic
- 245 10
- $a Protective effect of Clostridium tyrobutyricum in acute dextran sodium sulphate-induced colitis: differential regulation of tumour necrosis factor-α and interleukin-18 in BALB/c and severe combined immunodeficiency mice / $c T. Hudcovic, J. Kolinska, J. Klepetar, R. Stepankova, T. Rezanka, D. Srutkova, M. Schwarzer, V. Erban, Z. Du, JM. Wells, T. Hrncir, H. Tlaskalova-Hogenova, H. Kozakova
- 520 9_
- $a One of the promising approaches in the therapy of ulcerative colitis is administration of butyrate, an energy source for colonocytes, into the lumen of the colon. This study investigates the effect of butyrate producing bacterium Clostridium tyrobutyricum on dextran sodium sulphate (DSS)-induced colitis in mice. Immunocompetent BALB/c and immunodeficient severe combined immunodeficiency (SCID) mice reared in specific-pathogen-free (SPF) conditions were treated intrarectally with C. tyrobutyricum 1 week prior to the induction of DSS colitis and during oral DSS treatment. Administration of DSS without C. tyrobutyricum treatment led to an appearance of clinical symptoms - bleeding, rectal prolapses and colitis-induced increase in the antigen CD11b, a marker of infiltrating inflammatory cells in the lamina propria. The severity of colitis was similar in BALB/c and SCID mice as judged by the histological damage score and colon shortening after 7 days of DSS treatment. Both strains of mice also showed a similar reduction in tight junction (TJ) protein zonula occludens (ZO)-1 expression and of MUC-2 mucin depression. Highly elevated levels of cytokine tumour necrosis factor (TNF)-α in the colon of SCID mice and of interleukin (IL)-18 in BALB/c mice were observed. Intrarectal administration of C. tyrobutyricum prevented appearance of clinical symptoms of DSS-colitis, restored normal MUC-2 production, unaltered expression of TJ protein ZO-1 and decreased levels of TNF-α and IL-18 in the descending colon of SCID and BALB/c mice, respectively. Some of these features can be ascribed to the increased production of butyrate in the lumen of the colon and its role in protection of barrier functions and regulation of IL-18 expression.
- 650 _2
- $a akutní nemoc $7 D000208
- 650 _2
- $a aplikace rektální $7 D000285
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a antigeny CD11b $x biosyntéza $x genetika $7 D039481
- 650 _2
- $a bakteriální translokace $7 D018988
- 650 _2
- $a butyráty $x metabolismus $7 D002087
- 650 _2
- $a Clostridium tyrobutyricum $x fyziologie $7 D048014
- 650 _2
- $a ulcerózní kolitida $x chemicky indukované $x genetika $x imunologie $x mikrobiologie $x patologie $7 D003093
- 650 _2
- $a kolon $x metabolismus $x mikrobiologie $x patologie $7 D003106
- 650 _2
- $a síran dextranu $x toxicita $7 D016264
- 650 _2
- $a mastné kyseliny $x metabolismus $7 D005227
- 650 _2
- $a imunokompetence $7 D007121
- 650 _2
- $a interleukin-18 $x biosyntéza $x genetika $7 D020382
- 650 _2
- $a membránové proteiny $x biosyntéza $x genetika $7 D008565
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši inbrední BALB C $7 D008807
- 650 _2
- $a myši SCID $7 D016513
- 650 _2
- $a mucin 2 $x biosyntéza $x genetika $7 D055262
- 650 _2
- $a muciny $x biosyntéza $7 D009077
- 650 _2
- $a fosfoproteiny $x biosyntéza $x genetika $7 D010750
- 650 _2
- $a probiotika $x terapeutické užití $7 D019936
- 650 _2
- $a těžká kombinovaná imunodeficience $x genetika $x imunologie $7 D016511
- 650 _2
- $a organismy bez specifických patogenů $7 D013047
- 650 _2
- $a TNF-alfa $x biosyntéza $x genetika $7 D014409
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Kolínská, Jiřina $7 xx0106974 $u Institute of Physiology of the Academy of Sciences of the Czech Republic, v.v.i., Prague
- 700 1_
- $a Klepetář, Jan, $d 1949- $7 xx0154443 $u Institute of Physiology of the Academy of Sciences of the Czech Republic, v.v.i., Prague
- 700 1_
- $a Štěpánková, Renata $7 xx0246647 $u Institute of Microbiology of the Academy of Sciences of the Czech Republic, v.v.i., Prague
- 700 1_
- $a Řezanka, Tomáš $7 xx0106317 $u Institute of Microbiology of the Academy of Sciences of the Czech Republic, v.v.i., Prague
- 700 1_
- $a Šrůtková, Dagmar $u Institute of Microbiology of the Academy of Sciences of the Czech Republic, v.v.i., Prague
- 700 1_
- $a Schwarzer, Martin, $d 1980- $7 xx0128913 $u Institute of Microbiology of the Academy of Sciences of the Czech Republic, v.v.i., Prague
- 700 1_
- $a Erban, Vladimír, $d 1952- $7 xx0068152 $u Food Research Institute, Prague, Czech Republic
- 700 1_
- $a Du, Zhengyu $u Institute of Microbiology of the Academy of Sciences of the Czech Republic, v.v.i., Prague
- 700 1_
- $a Wells, J. M. $u Host-Microbe Interactomics, Animal Sciences, Wageningen University, Wageningen, The Netherlands
- 700 1_
- $a Hrnčíř, Tomáš $7 xx0241632 $u Institute of Microbiology of the Academy of Sciences of the Czech Republic, v.v.i., Prague
- 700 1_
- $a Tlaskalová, Helena, $d 1938- $7 jn20000402365 $u Institute of Microbiology of the Academy of Sciences of the Czech Republic, v.v.i., Prague
- 700 1_
- $a Kozáková, Hana, $d 1952- $7 xx0153144 $u Institute of Microbiology of the Academy of Sciences of the Czech Republic, v.v.i., Prague
- 773 0_
- $w MED00009471 $t Clinical and experimental immunology $x 1365-2249 $g Roč. 167, č. 2 (2012), s. 356-365
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/22236013 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m $z 0
- 990 __
- $a 20120806 $b ABA008
- 991 __
- $a 20160215094010 $b ABA008
- 999 __
- $a ok $b bmc $g 944096 $s 779480
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2012 $b 167 $c 2 $d 356-365 $i 1365-2249 $m Clinical and experimental immunology $n Clin Exp Immunol $x MED00009471
- LZP __
- $b NLK111 $a Pubmed-20120806/12/01