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      Effects of three immobilizing drug combinations on ventilation, gas exchange and metabolism in free-living African lions ( Panthera leo)

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          Abstract

          Free-living lions (12 per group) were immobilized with tiletamine-zolazepam-medetomidine (TZM), ketamine-medetomidine (KM), or ketamine-butorphanol-medetomidine (KBM). During immobilization, respiratory, blood gas and acid–base variables were monitored for 30 minutes. Respiratory rates were within expected ranges and remained constant throughout the immobilizations. Ventilation increased in lions over the immobilization period from 27.2 ± 9.5 to 35.1 ± 25.4 L/min (TZM), 26.1 ± 14.3 to 28.4 ± 18.4 L/min (KM) and 23.2 ± 10.8 to 26.7 ± 14.2 L/min (KBM). Tidal volume increased over the immobilization period from 1800 ± 710 to 2380 ± 1930 mL/breath (TZM), 1580 ± 470 to 1640 ± 500 mL/breath (KM) and 1600 ± 730 to 1820 ± 880 mL/breath (KBM). Carbon dioxide production was initially lower in KBM (0.4 ± 0.2 L/min) than in TZM (0.5 ± 0.2 L/min) lions but increased over time in all groups. Oxygen consumption was 0.6 ± 0.2 L/min (TZM), 0.5 ± 0.2 L/min (KM) and 0.5 ± 0.2 L/min (KBM) and remained constant throughout the immobilization period. Initially the partial pressure of arterial oxygen was lower in KBM (74.0 ± 7.8 mmHg) than in TZM (78.5 ± 4.7 mmHg) lions, but increased to within expected range in all groups over time. The partial pressure of arterial carbon dioxide was higher throughout the immobilizations in KBM (34.5 ± 4.2 mmHg) than in TZM (32.6 ± 2.2 mmHg) and KM (32.6 ± 3.8 mmHg) lions. Alveolar-arterial gradients were initially elevated, but decreased over time for all groups, although in KM lions it remained elevated (26.9 ± 10.4 mmHg) above the expected normal. Overall, all three drug combinations caused minor respiratory and metabolic side-effects in the immobilized lions. However, initially hypoxaemia occurred as the drug combinations, and possibly the stress induced by the immobilization procedure, hinder alveoli oxygen gas exchange.

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          G*Power 3: A flexible statistical power analysis program for the social, behavioral, and biomedical sciences

          G*Power (Erdfelder, Faul, & Buchner, 1996) was designed as a general stand-alone power analysis program for statistical tests commonly used in social and behavioral research. G*Power 3 is a major extension of, and improvement over, the previous versions. It runs on widely used computer platforms (i.e., Windows XP, Windows Vista, and Mac OS X 10.4) and covers many different statistical tests of the t, F, and chi2 test families. In addition, it includes power analyses for z tests and some exact tests. G*Power 3 provides improved effect size calculators and graphic options, supports both distribution-based and design-based input modes, and offers all types of power analyses in which users might be interested. Like its predecessors, G*Power 3 is free.
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              Immobilization of polar bears (Ursus maritimus) with Telazol in the Canadian Arctic.

              In 1986, 213 polar bears (Ursus maritimus) were immobilized with Telazol on the sea ice of the eastern Beaufort Sea during April and May, and 106 along the western coast of Hudson Bay near Churchill, Manitoba (Canada) in September. No animals died from handling. The efficacy of this drug at different seasons and the physiological responses of the immobilized bears were compared. A single injection of 8 to 9 mg of Telazol per kg of body weight gave a rapid full immobilization with satisfactory analgesia, and faster recovery than other drugs for which there is no antagonist. The reactions of the bears could be reliably and easily interpreted from a safe distance before the animal was approached. There was a wide range of tolerance to high dosages and bears appeared able to thermoregulate while immobilized. The mortality rate due to handling was lower than with any other drug used to date.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                Conserv Physiol
                Conserv Physiol
                conphys
                Conservation Physiology
                Oxford University Press
                2051-1434
                2023
                10 August 2023
                10 August 2023
                : 11
                : 1
                : coad059
                Affiliations
                Department of Paraclinical Sciences, Faculty of Veterinary Science, University of Pretoria , Soutpan Road, Onderstepoort, Pretoria, Gauteng, South Africa, 0110
                Centre for Veterinary Wildlife Research, Faculty of Veterinary Science, University of Pretoria , Soutpan Road, Onderstepoort, Pretoria, Gauteng, South Africa, 0110
                Center for Zoo and Wild Animal Health, Copenhagen Zoo , Frederiksberg, Denmark, 2000
                Brain Function Research Group, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand , York Road, Parktown, Johannesburg, Gauteng, South Africa, 2193
                Centre for Veterinary Wildlife Research, Faculty of Veterinary Science, University of Pretoria , Soutpan Road, Onderstepoort, Pretoria, Gauteng, South Africa, 0110
                Veterinary Wildlife Services, South African National Parks, Kruger National Park , Skukuza, Mpumalanga, South Africa, 1350
                Department of Production Animal Studies, Faculty of Veterinary Science, University of Pretoria , Soutpan Road, Onderstepoort, Pretoria, Gauteng, South Africa, 0110
                Department of Paraclinical Sciences, Faculty of Veterinary Science, University of Pretoria , Soutpan Road, Onderstepoort, Pretoria, Gauteng, South Africa, 0110
                Centre for Veterinary Wildlife Research, Faculty of Veterinary Science, University of Pretoria , Soutpan Road, Onderstepoort, Pretoria, Gauteng, South Africa, 0110
                Brain Function Research Group, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand , York Road, Parktown, Johannesburg, Gauteng, South Africa, 2193
                Department of Paraclinical Sciences, Faculty of Veterinary Science, University of Pretoria , Soutpan Road, Onderstepoort, Pretoria, Gauteng, South Africa, 0110
                Centre for Veterinary Wildlife Research, Faculty of Veterinary Science, University of Pretoria , Soutpan Road, Onderstepoort, Pretoria, Gauteng, South Africa, 0110
                Brain Function Research Group, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand , York Road, Parktown, Johannesburg, Gauteng, South Africa, 2193
                Author notes
                Corresponding author: Department of Paraclinical Sciences, Faculty of Veterinary Science, University of Pretoria, Soutpan Road, Onderstepoort, Pretoria, Gauteng, South Africa, 0110. Tel: +27117172152. E-mail: acdonaldson@ 123456gmail.com
                Article
                coad059
                10.1093/conphys/coad059
                10416691
                bd3ef914-1105-4264-a367-050675bb1d4b
                © The Author(s) 2023. Published by Oxford University Press and the Society for Experimental Biology.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 24 April 2023
                : 26 June 2023
                : 23 July 2023
                : 16 July 2023
                Page count
                Pages: 13
                Categories
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                AcademicSubjects/SCI00840

                a-a gradient,butorphanol,hypoxaemia,ketamine,medetomidine
                a-a gradient, butorphanol, hypoxaemia, ketamine, medetomidine

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