Literature DB >> 27261270

VBP15, a novel dissociative steroid compound, reduces NFκB-induced expression of inflammatory cytokines in vitro and symptoms of murine trinitrobenzene sulfonic acid-induced colitis.

Jesse M Damsker1, Laurie S Conklin2,3, Soheil Sadri2,3, Blythe C Dillingham4, Karuna Panchapakesan4, Christopher R Heier4, John M McCall5,6, Anthony D Sandler2,3.   

Abstract

OBJECTIVE AND
DESIGN: The goal of this study was to assess the capacity of VBP15, a dissociative steroidal compound, to reduce pro-inflammatory cytokine expression in vitro, to reduce symptoms of colitis in the trinitrobenzene sulfonic acid-induced murine model, and to assess the effect of VBP15 on growth stunting in juvenile mice. MATERIALS: In vitro studies were performed in primary human intestinal epithelial cells. Colitis was induced in mice by administering trinitrobenzene sulfonic acid. Growth stunting studies were performed in wild type outbred mice. TREATMENT: Cells were treated with VBP15 or prednisolone (10 μM) for 24 h. Mice were subjected to 3 days of VBP15 (30 mg/kg) or prednisolone (30 mg/kg) in the colitis study. In the growth stunting study, mice were subjected to VBP15 (10, 30, 45 mg/kg) or prednisolone (10 mg/kg) for 5 weeks.
METHODS: Cytokines were measured by PCR and via Luminex. Colitis symptoms were evaluated by assessing weight loss, intestinal blood, and stool consistency. Growth stunting was assessed using an electronic caliper.
RESULTS: VBP15 significantly reduced the in vitro production of CCL5 (p < 0.001) IL-6 (p < 0.001), IL-8 (p < 0.05) and reduced colitis symptoms (p < 0.05). VBP15 caused less growth stunting than prednisolone (p < 0.001) in juvenile mice.
CONCLUSION: VBP15 may reduce symptoms of IBD, while decreasing or avoiding detrimental side effects.

Entities:  

Keywords:  Autoimmunity; Glucocorticoids; Inflammation; Inflammatory bowel disease

Mesh:

Substances:

Year:  2016        PMID: 27261270     DOI: 10.1007/s00011-016-0956-8

Source DB:  PubMed          Journal:  Inflamm Res        ISSN: 1023-3830            Impact factor:   4.575


  35 in total

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Journal:  Curr Opin Pharmacol       Date:  2010-05-20       Impact factor: 5.547

2.  DNA binding of the glucocorticoid receptor is not essential for survival.

Authors:  H M Reichardt; K H Kaestner; J Tuckermann; O Kretz; O Wessely; R Bock; P Gass; W Schmid; P Herrlich; P Angel; G Schütz
Journal:  Cell       Date:  1998-05-15       Impact factor: 41.582

3.  Selective glucocorticoid receptor agonists for the treatment of inflammatory bowel disease: studies in mice with acute trinitrobenzene sulfonic acid colitis.

Authors:  Kerstin C Reuter; Christian R Grunwitz; Bettina M Kaminski; Dieter Steinhilber; Heinfried H Radeke; Jürgen Stein
Journal:  J Pharmacol Exp Ther       Date:  2012-01-10       Impact factor: 4.030

4.  Glucocorticoid-mediated repression of nuclear factor-kappaB-dependent transcription involves direct interference with transactivation.

Authors:  K De Bosscher; M L Schmitz; W Vanden Berghe; S Plaisance; W Fiers; G Haegeman
Journal:  Proc Natl Acad Sci U S A       Date:  1997-12-09       Impact factor: 11.205

5.  Cell specific effects of glucocorticoid treatment on the NF-kappaBp65/IkappaBalpha system in patients with Crohn's disease.

Authors:  K Thiele; A Bierhaus; F Autschbach; M Hofmann; W Stremmel; H Thiele; R Ziegler; P P Nawroth
Journal:  Gut       Date:  1999-11       Impact factor: 23.059

Review 6.  NF-kappaB in inflammatory bowel disease.

Authors:  I Atreya; R Atreya; M F Neurath
Journal:  J Intern Med       Date:  2008-06       Impact factor: 8.989

7.  Nuclear factor-kappa B repression in antiinflammation and immunosuppression by glucocorticoids.

Authors:  B van der Burg; J Liden; S Okret; F Delaunay; S Wissink; P T van der Saag; J A Gustafsson
Journal:  Trends Endocrinol Metab       Date:  1997 May-Jun       Impact factor: 12.015

8.  Abrogation of glucocorticoid receptor dimerization correlates with dissociated glucocorticoid behavior of compound a.

Authors:  Steven Robertson; Fatima Allie-Reid; Wim Vanden Berghe; Koch Visser; Anke Binder; Donita Africander; Michael Vismer; Karolien De Bosscher; Janet Hapgood; Guy Haegeman; Ann Louw
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Authors:  Jesse M Damsker; Blythe C Dillingham; Mary C Rose; Molly A Balsley; Christopher R Heier; Alan M Watson; Erik J Stemmy; Roslyn A Jurjus; Tony Huynh; Kathleen Tatem; Kitipong Uaesoontrachoon; Dana M Berry; Angela S Benton; Robert J Freishtat; Eric P Hoffman; John M McCall; Heather Gordish-Dressman; Stephanie L Constant; Erica K M Reeves; Kanneboyina Nagaraju
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Journal:  Sci Rep       Date:  2015-09-15       Impact factor: 4.379

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4.  Exposure-Response Analysis of Vamorolone (VBP15) in Boys With Duchenne Muscular Dystrophy.

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6.  The corticosteroid compounds prednisolone and vamorolone do not alter the nociception phenotype and exacerbate liver injury in sickle cell mice.

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Journal:  Sci Rep       Date:  2018-04-17       Impact factor: 4.379

7.  Phase 1 trial of vamorolone, a first-in-class steroid, shows improvements in side effects via biomarkers bridged to clinical outcomes.

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Journal:  Steroids       Date:  2018-03-08       Impact factor: 2.668

Review 8.  The Role of Glucocorticoids in Inflammatory Diseases.

Authors:  Sybille D Reichardt; Agathe Amouret; Chiara Muzzi; Sabine Vettorazzi; Jan P Tuckermann; Fred Lühder; Holger M Reichardt
Journal:  Cells       Date:  2021-10-28       Impact factor: 6.600

9.  Identification of Pathway-Specific Serum Biomarkers of Response to Glucocorticoid and Infliximab Treatment in Children with Inflammatory Bowel Disease.

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Journal:  Clin Transl Gastroenterol       Date:  2016-09-15       Impact factor: 4.488

10.  Vamorolone trial in Duchenne muscular dystrophy shows dose-related improvement of muscle function.

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