Anti‐inflammatory and anti‐hyperalgesic effects induced by an aqueous aged black garlic extract in rodent models of ulcerative colitis and colitis‐associated visceral pain

Author:

Libero Maria Loreta12,Lucarini Elena3,Recinella Lucia1ORCID,Ciampi Clara3,Veschi Serena1,Piro Anna1,Chiavaroli Annalisa1,Acquaviva Alessandra1,Nilofar Nilofar1,Orlando Giustino1ORCID,Generali Daniele45,Ghelardini Carla3,di Cesare Mannelli Lorenzo3ORCID,Montero‐Hidalgo Antonio J.2678,Luque Raúl M.2678,Ferrante Claudio1,Menghini Luigi1,di Simone Simonetta Cristina1,Brunetti Luigi1ORCID,Leone Sheila1

Affiliation:

1. Department of Pharmacy “G. d'Annunzio” University Chieti Italy

2. Department of Cell Biology, Physiology and Immunology University of Cordoba Cordoba Spain

3. Department of Neuroscience, Psychology, Drug Research and Child Health—NEUROFARBA—Pharmacology and Toxicology Section University of Florence Florence Italy

4. Department of Medical, Surgical and Health Sciences University of Trieste Trieste Italy

5. Department of Advanced Translational Microbiology Institute for Maternal and Child Health‐IRCCS “Burlo Garofolo” Trieste Italy

6. Maimonides Biomedical Research Institute of Cordoba (IMIBIC) Cordoba Spain

7. Reina Sofia University Hospital (HURS) Cordoba Spain

8. Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y Nutrición (CIBERobn) Cordoba Spain

Abstract

AbstractInflammatory bowel disease (IBD) is a morbid condition characterized by relapsing–remitting inflammation of the colon, accompanied by persistent gut dysmotility and abdominal pain. Different reports demonstrated biological activities of aged black garlic (ABG), including anti‐inflammatory and antioxidant effects. We aimed to investigate beneficial effects exerted by ABGE on colon inflammation by using ex vivo and in vivo experimental models. We investigated the anti‐inflammatory effects of an ABG water extract (ABGE) on rat colon specimens exposed to E. coli lipopolysaccharide (LPS), a known ex vivo experimental model of ulcerative colitis. We determined gene expression of various biomarkers involved in inflammation, including interleukin (IL)‐1β, IL‐6, nuclear factor‐kB (NF‐kB), tumor necrosis factor (TNF)‐α. Moreover, we studied the acute effects of ABGE on visceral pain associated with colitis induced by 2,4‐di‐nitrobenzene sulfonic acid (DNBS) injection in rats. ABGE suppressed LPS‐induced gene expression of IL‐1β, IL‐6, NF‐kB, and TNF‐α. In addition, the acute administration of ABGE (0.03–1 g kg−1) dose‐dependently relieved post‐inflammatory visceral pain, with the higher dose (1 g kg−1) able to significantly reduce both the behavioral nociceptive response and the entity of abdominal contraction (assessed by electromyography) in response to colorectal distension after the acute administration in DNBS‐treated rats. Present findings showed that ABGE could represent a potential strategy for treatment of colitis‐associated inflammatory process and visceral pain. The beneficial effects induced by the extract could be related to the pattern of polyphenolic composition, with particular regard to gallic acid and catechin.

Publisher

Wiley

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