Abstract

Evidence for beneficial effects of corticotropin releasing hormone (CRH) antagonists in abdominal and pelvic organs is emerging in preclinical studies. Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement a compilation of preclinical studies using CRH receptor antagonists as a treatment for abdominal and pelvic disease was carried out. The Animal Research: Reporting of In Vivo Experiments (ARRIVE) essential 10 guidelines were used to determine quality of the included studies. A total of 40 studies from the last 15 years studying irritable bowel syndrome, inflammatory bowel disease, endometriosis, enteritis, stress impact on gastrointestinal processes and exogenous CRH administration effects were included. Blockage of the CRH receptor 1 was mainly associated with beneficial effects while that of CRH receptor 2 worsened studied effects. However, time of administration, route of administration and the animal model used, all had an impact on the beneficial outcomes. Frequency of drugs administered indicated that astressin-2B, astressin and antalarmin were among the most utilized antagonists. Of concern, studies included were predominantly carried out in male models only, representing a gender discrepancy in preclinical studies compared to the clinical scenario. The ARRIVE score average was 13 with ~60% of the studies failing to randomize or blind the experimental units. Despite the failure to date of the CRH antagonists in moving across the clinical trials pipeline, there is evidence for their beneficial effects beyond mood disorders. Future pre-clinical studies should be tailored towards effectively predicting the clinical scenario, including reduction of bias and randomization.

Highlights

  • ObjectivesThe overall goal of this review was to systematically synthesize the available evidence for the use of Corticotropin-releasing hormone (CRH) antagonists for disorders associated with abdominal and pelvic organs

  • Most preclinical studies in this review found that Corticotropin-releasing hormone (CRH)-R1 antagonists can inhibit or diminish gastrointestinal symptoms and reduce stress-induced symptoms caused by CRH administration, perhaps by inhibiting CRH receptor type 1 (CRH-R1) receptor-mediated inflammation

  • Current pharmacological treatments for irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD) are based on improving disease symptoms but not curing these diseases, and many treatments are known to cause adverse effects

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Summary

Objectives

The overall goal of this review was to systematically synthesize the available evidence for the use of CRH antagonists for disorders associated with abdominal and pelvic organs

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