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  • Author or Editor: Mitsuyoshi Hagio x
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SUMMARY

To measure the concentration of serum amyloid A (saa) protein in horses, a sensitive and highly reproducible sandwich (elisa) was established, using affinity purified saa antibody. Results of the elisa were found to have a high correlation (r = 0.95) with those of the single radial immunodiffusion test. Equine saa concentration was measured by use of this elisa. In clinically normal horses, the concentration of saa was high immediately after birth to 2 weeks of age. After that, saa concentration had periodic fluctuations in the range of approximately 10 to 30 μg/ml. Mean (± sd) concentrations of saa in foals (≤ 12 months old) and adult horses (≥ 18 months old) were 21.23 ± 12.20 and 14.93 ± 9.07 μg/ml, respectively. In mares during the perinatal period, saa concentration remained stable within the reference range before parturition. It increased quickly after delivery, and reached a peak value of 101.29 ± 98.82 μg/ml on postpartum day 3, then began to decrease, at postpartum week 2, to the reference range by the end of postpartum month 1. In horses with experimentally induced inflammation, saa concentration increased quickly and reached approximately four- to 40-fold increase over the pretreatment value on day 1 and remained high on days 2 to 6 after treatment. It then returned to the baseline value by 2 to 4 weeks in association with disappearance of local signs of inflammation. The saa concentration was high in most horses with clinical signs of inflammation. It was concluded from these data that this elisa is sensitive and reliable for measuring saa in horses.

Free access
in American Journal of Veterinary Research

Abstract

Objective—To determine effects of hypercapnia on arrhythmias in ducks anesthetized with halothane.

Animals—12 ducks, 6 to 8 months old, weighing 1.1 to 1.6 kg.

Procedures—Each duck was anesthetized with a 1.5% mixture of halothane in oxygen, and anesthetic depth was stabilized during a 20-minute period. We added CO2 to the inspired oxygen to produce CO2 partial pressures of 40, 60, and 80 mm Hg in the inspired gas mixture. The CO2 partial pressure was increased in a stepwise manner. When arrhythmias were not evident during inhalation of the gas mixture at a specific CO2 partial pressure, the CO2 partial pressure was maintained for 10 minutes before a sample was collected for blood gas analysis. When arrhythmias were detected, a sample for blood gas analysis was collected after the CO2 partial pressure was maintained for at least 2 minutes, and CO2 inhalation then was terminated.

Results—During the stabilization period, PaCO2 (mean ± SD) was 33 ± 5 mm Hg,and arrhythmias were not detected. In 6 ducks, arrhythmias such as unifocal and multifocal premature ventricular contractions developed during inhalation of CO2. Mean PaCO2 at which arrhythmias developed was 67 ± 12 mm Hg. In 5 of 6 ducks with arrhythmias, the arrhythmias disappeared after CO2 inhalation was terminated.

Conclusion and Clinical Relevance—Analysis of data from this study indicated that hypercapnia can lead to arrhythmias in ducks during halothane-induced anesthesia. Thus, ventilatory support to maintain normocapnia is important for managing ducks anesthetized with halothane. ( Am J Vet Res 2001;62: 127–129)

Full access
in American Journal of Veterinary Research

Abstract

Objective—To determine the cardiorespiratory effects of epidural administration of morphine alone and in combination with fentanyl in dogs anesthetized with sevoflurane.

Design—Prospective study.

Animals—6 dogs.

Procedure—Dogs were anesthetized with sevoflurane and allowed to breathe spontaneously. After a stable plane of anesthesia was achieved, morphine (0.1 mg/kg [0.045 mg/lb]) or a combination of morphine and fentanyl (10 µg/kg [4.5 µg/lb) was administered through an epidural catheter, the tip of which was positioned at the level of L6 or L7. Cardiorespiratory variables were measured for 90 minutes.

Results—Epidural administration of morphine alone did not cause any significant changes in cardiorespiratory measurements. However, epidural administration of morphine and fentanyl induced significant decreases in diastolic and mean arterial blood pressures and total peripheral resistance. Stroke volume was unchanged, PaCO2 was significantly increased, and arterial pH and base excess were significantly decreased. Heart rate was significantly lower after epidural administration of morphine and fentanyl than after administration of morphine alone. None of the dogs had any evidence of urine retention, vomiting, or pruritus after recovery from anesthesia.

Conclusions and Clinical Relevance—Results suggest that epidural administration of morphine at a dose of 0.1 mg/kg in combination with fentanyl at a dose of 10 µg/kg can cause cardiorespiratory depression in dogs anesthetized with sevoflurane. (J Am Vet Med Assoc 2004;224:67–70)

Full access
in Journal of the American Veterinary Medical Association