Peer-reviewed veterinary case report
How dexmedetomidine and MK-467 affect low blood sugar in dogs
By Kallio-Kujala, I J et al.·Published in Veterinary journal (London, England : 1997)·2018·Department of Equine and Small Animal Medicine·View original on PubMed →
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Original publication title: Effects of dexmedetomidine and MK-467 on plasma glucose, insulin and glucagon in a glibenclamide-induced canine hypoglycaemia model.
- Species:
- dog
Plain-English summary
A group of eight beagle dogs was tested to see how two drugs, dexmedetomidine and MK-467, affected blood sugar levels after inducing low blood sugar (hypoglycemia) with another medication called glibenclamide. While glibenclamide caused insulin release and lowered blood sugar, dexmedetomidine helped prevent this drop. However, when MK-467 was added, it stimulated insulin release, which could be risky for dogs prone to low blood sugar. Fortunately, none of the dogs experienced severe hypoglycemia during the study, suggesting that the combination of these drugs can be safe, but caution is advised for dogs at risk of low blood sugar.
People also search for: dog low blood sugar treatment · dexmedetomidine effects on dogs · MK-467 for dogs hypoglycemia
Abstract
The commonly used sedative α-adrenoceptor agonist dexmedetomidine has adverse cardiovascular effects in dogs that can be prevented by concomitant administration of the peripherally acting α-adrenoceptor antagonist MK-467. An ancillary effect of dexmedetomidine is to decrease insulin release from the pancreas, whereas MK-467 stimulates insulin release. This study assessed the effects of co-administered dexmedetomidine and MK-467 in a canine glibenclamide-induced hypoglycaemia model. In a randomised, cross-over experiment, eight beagle dogs received five intravenous treatments, comprising two administrations of saline, with dexmedetomidine or dexmedetomidine and MK-467, and three administrations of glibenclamide, with saline, dexmedetomidine or dexmedetomidine and MK-467. Plasma concentrations of glucose, lactate, insulin, glucagon and the test drugs were monitored. Administration of glibenclamide significantly increased insulin secretion and decreased blood glucose concentrations. Dexmedetomidine counteracted glibenclamide-evoked hypoglycaemia. This was opposed by the α-adrenoceptor antagonist MK-467, but the glibenclamide-evoked hypoglycaemia was not potentiated by co-administration of dexmedetomidine and MK-467. None of the dogs developed uncontrolled hypoglycaemia. Thus, the combination of dexmedetomidine and MK-467 appeared to be safe in this canine hypoglycaemia model. Nevertheless, when MK-467 is used to alleviate the undesired cardiovascular effects of α-adrenoceptor agonists in dogs, it should be used with caution in animals at risk for hypoglycaemia because of its insulin-releasing and hypoglycaemic effects.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/30503541/