Influence of atipamezole on effects of midsacral subarachnoidally administered detomidine in mares.
Abstract: To examine effects of atipamezole on detomidine midsacral subarachnoidally-induced analgesia, cardiovascular and respiratory activity, head ptosis, and position of pelvic limbs in healthy mares. Methods: 10 healthy mares. Methods: Using a randomized, blinded, crossover study design, mares received detomidine (0.03 mg/kg of body weight, diluted in 3 ml of CSF) midsacral subarachnoidally, followed by atipamezole (0.1 mg/kg [test]) or sterile saline (0.9% NaCl) solution (control), i.v. 61 minutes later and saline solution (3 ml, midsacral subarachnoidally) on a separate occasion, at least 2 weeks later. Analgesia was determined by lack of sensory perception to electrical stimulation at the perineal dermatome and no response to needle-prick stimulation extending from the coccygeal to T15 dermatomes. Arterial acid-base (pH, standard bicarbonate, and base excess values), gas tensions (PO2, PCO2), PCV, total solids concentration, heart and respiratory rates, rectal temperature, and arterial blood pressure were determined, and mares were observed for sweating and urination. Mean scores of perineal analgesia, head ptosis, position of pelvic limbs, and cardiovascular and respiratory data were compared for the 3-hour test period. Results: Subarachnoidally administered detomidine induced perineal analgesia (mean +/- SD onset, 9.0 +/- 4.6 minutes; duration, 130 +/- 26 minutes), marked head ptosis, moderate changes in pelvic limb position, cardiovascular and respiratory depression, sweating in analgesic zones, and diuresis. Intravenously administered atipamezole significantly reduced mean scores of detomidine-induced perineal analgesia, head ptosis, pelvic limb position, sweating and diuresis; partially antagonized detomidine-induced bradycardia; and did not effect detomidine-induced bradypnea. Conclusions: Most effects of midsacral subarachnoidally administered detomidine, except bradycardia and bradypnea, were reversed by atipamezole (0.1 mg/kg, i.v.), indicating that most of the actions of detomidine were mediated via activation of alpha2-adrenergic receptors.
Publication Date: 1998-05-01 PubMed ID: 9563633
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research investigates the impact of using atipamezole on mares who have been administered detomidine, examining effects on pain relief, cardiovascular and respiratory function, and limb positioning. The study indicates atipamezole can reverse most effects of detomidine, apart from decreases in heart and breath rate.
Study Design
- The study was conducted using a sample of 10 healthy mares, with a randomized, blinded, and crossover study design.
- Each subject was given detomidine, dissolved in 3 ml of Cerebrospinal fluid (CSF), through midsacral subarachnoidally, followed by either atipamezole or sterile saline solution 61 minutes later as a test or control condition.
- These were administered intravenously. The mares then received a saline solution, again through midsacral subarachnoidally, two weeks later.
Determination of Analgesia and Monitoring
- Analgesia was determined through the inability to perceive sensory stimulation at the perineal dermatome and non-responsiveness to needle-prick stimulation, ranging from the coccygeal to T15 dermatomes.
- Several physiological measures, such as arterial acid-base content, gas tensions, PCV, total solids concentration, heart and respiratory rates, and rectal temperature and arterial blood pressure, were measured.
- The mares were also observed for sweating and urination.
Results of Subarachnoidally Administered Detomidine
- The administration of detomidine resulted in pain relief in the perineal area, significant head drooping, changes in limb position, cardiovascular and respiratory depression, sweating in areas experiencing analgesia, and increased urination.
- The average onset of perineal analgesia was around 9 minutes, lasting approximately 130 minutes.
Effects of Atipamezole on Detomidine
- On the other hand, atipamezole effectively reduced the scores of detomidine-induced pain relief, head drooping, changes in limb position, sweating, and diuresis.
- Atipamezole was also found to partially counteract the decrease in heart rate caused by detomidine, but it did not affect the detomidine-induced decrease in breath rate.
Conclusion
- The study concluded that most of the effects of detomidine, except for slowing of heart and breath rates, could be reversed using atipamezole.
- This suggests that most of the impacts of detomidine are likely through the activation of alpha2-adrenergic receptors on the cell surface.
Cite This Article
APA
Skarda RT, Muir WW.
(1998).
Influence of atipamezole on effects of midsacral subarachnoidally administered detomidine in mares.
Am J Vet Res, 59(4), 468-477.
Publication
Researcher Affiliations
- Department of Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University, Columbus 43210-1089, USA.
MeSH Terms
- Acid-Base Equilibrium / drug effects
- Adrenergic alpha-Antagonists / pharmacology
- Analgesics / administration & dosage
- Analgesics / pharmacology
- Animals
- Blood Pressure / drug effects
- Body Temperature / drug effects
- Cross-Over Studies
- Drug Interactions
- Electric Stimulation
- Female
- Heart Rate / drug effects
- Horses
- Imidazoles / administration & dosage
- Imidazoles / pharmacology
- Pain
- Random Allocation
- Respiration / drug effects
- Sacrum
- Sensation / drug effects
- Single-Blind Method
- Subarachnoid Space
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