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Peer-reviewed veterinary case report

How a mutation in a dog's glucocorticoid receptor affects steroid

By Kosei Yamanaka et al.·Published in BMC Veterinary Research·2019·Laboratory of Molecular Diagnostics and Therapeutics, Joint Faculty of Veterinary Medicine, Yamaguchi University, GB·View original on DOAJ

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Original publication title: Functional characterization of canine wild type glucocorticoid receptor and an insertional mutation in a dog

Species:
dog

Plain-English summary

A dog with suspected iatrogenic Cushing syndrome (a condition caused by excessive glucocorticoid use) was found to have a genetic mutation affecting its glucocorticoid receptor (GR). This mutation resulted in a shorter version of the GR that did not respond well to prednisolone, a common glucocorticoid medication. While the study could not determine the exact clinical significance of this mutation, it highlights how some dogs may react differently to glucocorticoids due to genetic factors. Understanding these differences can help veterinarians tailor treatments for dogs with conditions requiring glucocorticoids.

People also search for: dog Cushing syndrome symptoms · glucocorticoid sensitivity in dogs · prednisolone side effects in dogs

Abstract

Abstract Background Glucocorticoids, among the most widely utilized drugs in veterinary medicine, are employed to treat a wide variety of diseases; however, their use often induces adverse events in dogs. The efficacy of glucocorticoids usually depends on dosage, although differences in sensitivity to glucocorticoids in individual animals have been reported. Glucocorticoids bind to the cytoplasmic glucocorticoid receptor (GR), which is expressed in almost all cells. These receptors are key factors in determining individual sensitivity to glucocorticoids. This study examined individual differences in glucocorticoid sensitivity in dogs, focusing on reactivity of the GR to prednisolone. Results We first molecularly cloned the GR gene from a healthy dog. We discovered a mutant GR in a dog suspected to have iatrogenic Cushing syndrome. The mutant GR had extra nucleotides between exons 6 and 7, resulting in a truncated form of GR that was 98 amino acids shorter than the wild-type dog GR. The truncated GR exhibited very low reactivity to prednisolone, irrespective of concentration. Conclusions We have identified the truncated form of canine GR in a dog with iatrogenic Cushing syndrome. This truncated form showed the very less sensitivity to glucocorticoid in vitro, unfortunately, we could not elucidate its clinical significance. However, our data is a first report about the function of canine GR, and will facilitate the analysis of canine glucocorticoid sensitivity.

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Original publication on DOAJ: https://doi.org/10.1186/s12917-019-2129-9