PUBLICATION

Intestinal Transit Time and Cortisol-Mediated Stress in Zebrafish

Authors
Brady, C., Denora, M., Shannon, I., Clark, K.J., Rich, A.
ID
ZDB-PUB-170721-2
Date
2017
Source
Zebrafish   14(5): 404-410 (Journal)
Registered Authors
Clark, Karl, Rich, Adam
Keywords
intestine, motility, stress
MeSH Terms
  • Animals
  • Animals, Genetically Modified/physiology*
  • Anti-Inflammatory Agents/pharmacology
  • Embryo, Nonmammalian/cytology
  • Embryo, Nonmammalian/drug effects
  • Embryo, Nonmammalian/physiology
  • Gastrointestinal Motility/drug effects
  • Gastrointestinal Tract/pathology*
  • Gastrointestinal Transit
  • Hydrocortisone/pharmacology*
  • Larva/drug effects
  • Larva/physiology
  • Receptors, Glucocorticoid/metabolism
  • Stress, Physiological/drug effects*
  • Zebrafish/physiology*
PubMed
28727940 Full text @ Zebrafish
Abstract
Intestinal motility, the spontaneous and rhythmic smooth muscle contraction, is a complex process that is regulated by overlapping and redundant regulatory mechanisms. Primary regulators intrinsic to the gastrointestinal tract include interstitial cells of Cajal, enteric neurons, and smooth muscle cells. Extrinsic primary regulators include the autonomic nervous system, immune system, and the endocrine system. Due to this complexity, a reductionist approach may be inappropriate if the ultimate goal is to understand motility regulation in vivo. Motility can be directly visualized in intact zebrafish, with intact regulatory systems, because larvae are transparent. Intestinal motility can therefore be measured in a complete system. However, the intestinal tract may respond to external influences, such as handling, which may invoke a stress response and influence intestinal transit. We used SR4G transgenic zebrafish, which express green fluorescent protein following activation of glucocorticoid receptors, and showed that handling required for the intestinal motility assay induces stress. Separate experiments showed that exogenous application of hydrocortisone did not influence intestinal transit, suggesting that handling may not interfere with transit measurements in intact zebrafish larvae. These experiments contribute to further development of the zebrafish model for intestinal motility research.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping