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Alpha 2-adrenergic agonists are often used for sedation and, or, analgesia in dogs, but they are often associated with bradycardia and in some animals with atrioventricular heart block. In this study, atropine or glycopyrrolate either helped to maintain the heart rates or were effective in increasing reduced heart rates of dogs treated with medetomidine. In the process, however, cardiac dysrhythmias often developed. These dysrhythmias were predominantly associated with the combined responses to the medetomidine and the anticholinergic agent because there were no significant changes in respiratory function. A reduced blood oxygen content or increased blood carbon dioxide can contribute to cardiac irritability. Atropine and glycopyrrolate were more effective in preventing bradycardia and had less undesirable side effects when they were given before the administration of medetomidine.
Vet Rec 1991 Oct 05
PMID:Effects of anticholinergic treatment on the cardiac and respiratory systems in dogs sedated with medetomidine. 168 74

Cell distribution and the effects of 12 daily injections of 80 mg/kg pilocarpine or 5 mg/kg atropine were studied in rat tracheal epithelium. Ciliated, periodic-acid-Schiff-positive (PAS+), Alcian blue-positive (AB+), nonstaining, and basal cells were counted and their order of occurrence was recorded. Pilocarpine caused a decrease in ciliated and an increase in PAS+, basal, and nonstaining cell numbers. Atropine caused similar changes, although to a much lesser extent. AB+ cells were rare. Cell occurrence was randomized by computer, and comparisons with nonrandomized counts were made to discern between 1) differences in cell arrangement owed to variations in cell numbers, and 2) actual biases in cell distribution. In general, ciliated areas amounted to a few cells and were separated by nonciliated patches of comparable size. The grouping characteristics of cells supported the notion that basal cells were surrounded by their progeny and that daughter cells were displaced by siblings. It was concluded that the cells were not randomly distributed. Basal cells were dispersed, and probably immediately related to PAS+ cells but not to ciliated cells. A bias toward grouping implied concurrent differentiation of clusters of sibling cells. With drug treatment, a substantial increase in PAS+ cells without increase in cell concentration suggested a decrease in ciliated cell differentiation. Larger groups of secretory cells with treatment suggested cell division without differentiation through the basal cell pathway. Cholinergic agents were not the predominant modulators of this epithelium, and their effect was probably secondary to influence over mucociliary function.
Anat Rec 1989 Oct
PMID:Cell distribution in tracheal surface epithelium and the effects of long-term pilocarpine and atropine administration. 281 27

To test the hypothesis that acepromazine could potentiate the sedative actions and attenuate the pressor response induced by dexmedetomidine, the effects of acepromazine or atropine were compared in six healthy adult dogs treated with this alpha2-agonist. In a randomised block design, the dogs received intravenous doses of either physiological saline, 0.05 mg/kg acepromazine or 0.04 mg/kg atropine, 15 minutes before an intravenous dose of 5 microg/kg dexmedetomidine. The dogs' heart rate was reduced by 50 to 63 per cent from baseline and their mean arterial blood pressure was increased transiently from baseline for 20 minutes after the dexmedetomidine. Atropine prevented the alpha2-agonist-induced bradycardia and increased the severity and duration of the hypertension, but acepromazine did not substantially modify the cardiovascular effects of the alpha2-agonist, except for a slight reduction in the magnitude and duration of its pressor effects. The dexmedetomidine induced moderate to intense sedation in all the treatments, but the dogs' sedation scores did not differ among treatments. The combination of acepromazine with dexmedetomidine had no obvious advantages in comparison with dexmedetomidine alone, but the administration of atropine before dexmedetomidine is contraindicated because of a severe hypertensive response.
Vet Rec 2008 Jun 28
PMID:Sedative and cardiorespiratory effects of acepromazine or atropine given before dexmedetomidine in dogs. 1858 62