Massey Research Online - Browsing by Author "Meyer LCR"

Browsing by Author "Meyer LCR"

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A Comparison of Hematological, Immunological, and Stress Responses to Capture and Transport in Wild White Rhinoceros Bulls (Ceratotherium simum simum) Supplemented With Azaperone or Midazolam
(Frontiers Media S.A., 2020-10-20) Pohlin F; Hooijberg EH; Buss P; Huber N; Viljoen FP; Blackhurst D; Meyer LCR; Torrey S
Capture and transport are essential procedures for the management and conservation of southern white rhinoceroses (Ceratotherium simum simum), but are associated with stress-induced morbidity and mortality. To improve conservation efforts, it is crucial to understand the pathophysiology of rhinoceros stress responses and investigate drug combinations that could reduce these responses. In this study we measured rhinoceros stress responses to capture and transport by quantifying hematological and immunological changes together with adrenal hormone concentrations. We investigated whether the potent anxiolytic drug midazolam was able to mitigate these responses compared to azaperone, which is more commonly used during rhinoceros transport. Twenty three wild white rhinoceros bulls were transported for 6 h (280 km) within the Kruger National Park for reasons unrelated to this study. Rhinoceroses were immobilized with either etorphine-azaperone (group A, n = 11) or etorphine-midazolam (group M, n = 12) intramuscularly by darting from a helicopter. Azaperone (group A) or midazolam (group M) were re-administered intramuscularly every 2 h during transport. Serial blood samples were collected at capture (TC), the start of transport (T0) and after 6 h of transport (T6). Changes in hematological and immunological variables over time and between groups were compared using general mixed models. Increases in plasma epinephrine and serum cortisol concentrations indicated that rhinoceroses mounted a stress response to capture and transport. Packed cell volume decreased from TC to T6 indicating that stress hemoconcentration occurred at TC. Neutrophils progressively increased and lymphocytes and eosinophils progressively decreased from T0 to T6, resulting in an increase in neutrophil to lymphocyte ratio; a characteristic leukocyte response to circulating glucocorticoids. A reduction in serum iron concentrations may suggest the mounting of an acute phase response. Rhinoceroses experienced a decrease in unsaturated fatty acids and an increase in lipid peroxidation products at capture and toward the end of transport indicating oxidative stress. Midazolam, at the dose used in this study, was not able to mitigate adrenal responses to stress and appeared to directly influence leukocyte responses.
A comparison of immobilisation quality and cardiorespiratory effects of etorphine-azaperone versus etorphine-midazolam combinations in blesbok
(Medpharm Publications on behalf of the South African Veterinary Association, 2022-06-01) Laubscher LL; Meyer LCR; Laurence M; Raath JP; Pfitzer S
The study compared immobilisation of blesbok (Damaliscus pygargus phillipsi) with etorphine and azaperone vs etorphine and midazolam. Twelve female blesbok, weighing 59.4 ± 2.8 kg, were used. Each animal randomly received Treatment 1 (T1) (etorphine, 0.07 ± 0.003 mg/kg + azaperone, 0.36 ± 0.02 mg/kg) and Treatment 2 (T2) (etorphine, 0.07 ± 0.003 mg/kg + midazolam, 0.20 ± 0.01 mg/kg) with a one-week washout period between treatments. Induction times were recorded followed by physiological monitoring for 45 minutes of immobilisation. Immobilisation was reversed with naltrexone (20 mg per mg etorphine). Recovery times were also recorded. Induction, immobilisation and recovery were scored with subjective measures. Inductions and recoveries did not differ between combinations, but the quality of immobilisation was significantly better with T1. Rectal temperature and blood pressure were significantly lower during T1. Both treatments resulted in severe hypoxaemia and impaired gas exchange, although overall hypoxaemia was more pronounced for T1. Animals treated with T2, however, exhibited a deterioration in respiration as the monitoring period progressed, possibly as a result of impaired ventilatory muscle function due to the effects of midazolam. Both combinations are suitable for adequate immobilisation of blesbok and should be selected based on the specific capture situation. Supplementation with oxygen is highly recommended.
Capture and transport of white rhinoceroses (Ceratotherium simum) cause shifts in their fecal microbiota composition towards dysbiosis
(Oxford University Press and the Society for Experimental Biology, 2023-11-24) Pohlin F; Frei C; Meyer LCR; Roch F-F; Quijada NM; Conrady B; Neubauer V; Hofmeyr M; Cooper D; Stalder G; Wetzels SU; Fuller A
Translocations of Rhinocerotidae are commonly performed for conservation purposes but expose the animals to a variety of stressors (e.g. prolonged fasting, confinement, novel environment, etc.). Stress may change the composition of gut microbiota, which can impact animal health and welfare. White rhinoceroses in particular can develop anorexia, diarrhea and enterocolitis after translocation. The aim of this study was to investigate the associations of age, sex and translocation on the rhinoceros' fecal bacterial microbiota composition. fecal samples were collected from rhinoceroses at capture (n = 16) and after a >30-hour road transport (n = 7). DNA was isolated from these samples and submitted for 16S rRNA V3-V4 phylotyping. Alpha diversity indices of the rhinoceros' fecal microbiota composition of different age, sex and before and after transport were compared using non-parametric statistical tests and beta diversity indices using Permutational Multivariate Analysis Of Variance (PERMANOVA). Resulting P-values were alpha-corrected (Padj.). Alpha and beta diversity did not differ between rhinoceroses of different age and sex. However, there was a significant difference in beta diversity between fecal samples collected from adult animals at capture and after transport. The most abundant bacterial phyla in samples collected at capture were Firmicutes and Bacteroidetes (85.76%), represented by Lachnospiraceae, Ruminococcaceae and Prevotellaceae families. The phyla Proteobacteria (Padj. = 0.009) and Actinobacteria (Padj. = 0.012), amongst others, increased in relative abundance from capture to after transport encompassing potentially pathogenic bacterial families such as Enterobacteriaceae (Padj. = 0.018) and Pseudomonadaceae (Padj. = 0.022). Important commensals such as Spirochaetes (Padj. = 0.009), Fibrobacteres (Padj. = 0.018) and Lachnospiraceae (Padj. = 0.021) decreased in relative abundance. These results indicate that the stressors associated with capture and transport cause an imbalanced fecal microbiota composition in white rhinoceroses that may lead to potentially infectious intestinal disorders. This imbalance may result from recrudescence of normally innocuous pathogens, increased shedding of pathogens or increased vulnerability to new pathogens.
Cardiovascular effects of intravenous vatinoxan in wild boars (Sus scrofa) anaesthetised with intramuscular medetomidine-tiletamine-zolazepam
(John Wiley and Sons Ltd on behalf of British Veterinary Association, 2022-01-21) Einwaller J; Meyer LCR; Auer U; Raekallio M; Nowack J; Haw A; Vetter S; Painer J; Stalder G
Background: The potent sedative medetomidine is a commonly used adjunct for the immobilisation of non-domestic mammals. However, its use is associated with pronounced cardiovascular side effects, such as bradycardia, vasoconstriction and decreased cardiac output. We investigated the effects of the peripherally-acting alpha-2-adrenoceptor antagonist vatinoxan on cardiovascular properties in medetomidine-tiletamine-zolazepam anaesthetised wild boar (Sus scrofa). Methods: Twelve wild boars, anaesthetised twice with medetomidine (0.1 mg/kg) and tiletamine/zolazepam (2.5 mg/kg) IM in a randomised, crossover study, were administered (0.1 mg/kg) vatinoxan or an equivalent volume of saline IV (control). Cardiovascular variables, including heart rate (HR), mean arterial blood pressure (MAP), pulmonary artery pressure (PAP), pulmonary artery occlusion pressure (PAOP) and cardiac output (CO), were assessed 5 min prior to vatinoxan/saline administration until the end of anaesthesia 30 min later. Results: MAP (p < 0.0001), MPAP (p < 0.001) and MPAOP (p < 0.0001) significantly decreased from baseline after vatinoxan until the end of anaesthesia. HR increased significantly (p < 0.0001) from baseline after vatinoxan administration. However, the effect on HR subsided 3 min after vatinoxan. All variables remained constant after saline injection. There was no significant effect of vatinoxan or saline on CO. Conclusion: Vatinoxan significantly reduced systemic and pulmonary artery hypertension, induced by medetomidine in wild boar.
Chemical immobilisation of lions: weighing up drug effectiveness versus clinical effects
(Medpharm Publications on behalf of the South African Veterinary Association, 2023-06-01) Donaldson AC; Fuller A; Meyer LCR; Buss PE
Selection of an effective drug combination to immobilise African lions (Panthera leo) requires balancing immobilisation effectiveness with potential side effects. We compared the immobilisation effectiveness and changes to physiological variables induced by three drug combinations used for free-ranging African lions. The lions (12 animals per drug combination) were immobilised with tiletamine-zolazepam-medetomidine (TZM), ketamine-medetomidine (KM) or ketamine-butorphanol-medetomidine (KBM). Induction, immobilisation, and recovery were timed, evaluated using a scoring system, and physiological variables were monitored. The drugs used for immobilisation were antagonised with atipamezole and naltrexone. The quality of induction was rated as excellent for all drug combinations and induction times (mean ± SD) did not differ between the groups (10.54 ± 2.67 min for TZM, 10.49 ± 2.63 min for KM, and 11.11 ± 2.91 min for KBM). Immobilisation depth was similar over the immobilisation period in the TZM and KBM groups, and initially light, progressing to deeper in lions administered KM. Heart rate, respiratory rate and peripheral arterial haemoglobin saturation with oxygen were within the expected range for healthy, awake lions in all groups. All lions were severely hypertensive and hyperthermic throughout the immobilisation. Following antagonism of immobilising drugs, lions immobilised with KM and KBM recovered to walking sooner than those immobilised with TZM, at 15.29 ± 10.68 min, 10.88 ± 4.29 min and 29.73 ± 14.46 min, respectively. Only one lion in the KBM group exhibited ataxia during recovery compared to five and four lions in the TZM and KM groups, respectively. All three drug combinations provided smooth inductions and effective immobilisations but resulted in hypertension. KBM had an advantage of allowing for shorter, less ataxic recoveries.
Co-production and conservation physiology: outcomes, challenges and opportunities arising from reflections on diverse co-produced projects
(y Oxford University Press and the Society for Experimental Biology, 2025-07-18) Cooke SJ; Bett NN; Hinch SG; Adolph CB; Hasler CT; Howell BE; Schoen AN; Mullen EJ; Fangue NA; Todgham AE; Cheung MJ; Johnson RC; Olstad RS-T; Sisk M; Sisk CC; Franklin CE; Irwin RC; Irwin TR; Lewandrowski W; Tudor EP; Ajduk H; Tomlinson S; Stevens JC; Wilcox AAE; Giacinti JA; Provencher JF; Dupuis-Smith R; Dwyer-Samuel F; Saunders M; Meyer LCR; Buss P; Rummer JL; Bard B; Fuller A; Helmuth B
As a relatively nascent discipline, conservation physiology has struggled to deliver science that is relevant to decision-makers or directly useful to practitioners. A growing body of literature has revealed that co-produced research is more likely to generate knowledge that is not only relevant, but that is also embraced and actionable. Co-production broadly involves conducting research collaboratively, inclusively, and in a respectful and engaged manner - spanning all stages from identifying research needs to study design, data collection, interpretation and application. This approach aims to create actionable science and deliver meaningful benefits to all partners involved. Knowledge can be co-produced with practitioners/managers working for regulators or stewardship bodies, Indigenous communities and governments, industry (e.g. fishers, foresters, farmers) and other relevant actors. Using diverse case studies spanning issues, taxa and regions from around the globe, we explore examples of co-produced research related to conservation physiology. In doing so, we highlight benefits and challenges while also identifying lessons for others considering such an approach. Although co-production cannot guarantee the ultimate success of a project, for applied research (such as what conservation physiology purports to deliver), embracing co-production is increasingly regarded as the single-most important approach for generating actionable science to inform conservation. In that sense, the conservation physiology community would be more impactful and relevant if it became commonplace to embrace co-production as demonstrated by the case studies presented here.
Comparison of the cardiovascular effects of immobilization with three different drug combinations in free-ranging African lions
(Oxford University Press on behalf of The Society for Experimental Biology, 2023-01-12) Donaldson AC; Meyer LCR; Fuller A; Buss PE; Seebacher F
Thirty-six free-ranging lions (12 per group) were immobilized with tiletamine-zolazepam (Zoletil 0.6 mg/kg i.m.) plus medetomidine (0.036 mg/kg i.m.) (TZM), ketamine (3.0 mg/kg i.m.) plus medetomidine (0.036 mg/kg i.m.) (KM) or ketamine (1.2 mg/kg i.m.) plus butorphanol (0.24 mg/kg i.m.) plus medetomidine (0.036 mg/kg i.m.) (KBM). During immobilization cardiovascular variables were monitored at 5-minute intervals for a period of 30 minutes. Lions immobilized with all three drug combinations were severely hypertensive. Systolic arterial pressure was higher at initial sampling in lions immobilized with KM (237.3 ± 24.8 mmHg) than in those immobilized with TZM (221.0 ± 18.1 mmHg) or KBM (226.0 ± 20.6 mmHg) and decreased to 205.8 ± 19.4, 197.7 ± 23.7 and 196.3 ± 17.7 mmHg, respectively. Heart rates were within normal ranges for healthy, awake lions and decreased throughout the immobilization regardless of drug combination used. Lions immobilized with TZM had a higher occurrence (66%) of skipped heart beats than those immobilized with KBM (25%). The three drug combinations all caused negative cardiovascular effects, which were less when KBM was used, but adverse enough to warrant further investigations to determine if these effects can be reversed or prevented when these three combinations are used to immobilize free-living lions.
Comparison of the immobilisation and cardiorespiratory effects of thiafentanil-azaperone versus thiafentanil-medetomidine-azaperone in African buffalo (Syncerus caffer)
(Medpharm Publications on behalf of the South African Veterinary Association, 2024-03-01) Faber VE; Burroughs REJ; Meyer LCR; Hansen HJ; Gerber D; Koeppel KN
African buffalo (Syncerus caffer) are frequently immobilised for veterinary interventions, disease screening and translocations. Concerns over user and animal safety, costs, and irregularities in opioid supply, have led to the development of alternative immobilisation protocols. This study compared immobilisation of 12 boma-habituated African buffalo with thiafentanil-azaperone (TA) vs. thiafentanil-medetomidine-azaperone (TMA) in a randomised crossover study. Each buffalo received a combination of thiafentanil (6–7 mg) + azaperone (40 mg) and thiafentanil (1 mg) + medetomidine (3–4 mg) + azaperone (40 mg) with a three-week washout period between immobilisations. Induction and recovery times were recorded, quality of induction and immobilisation were scored subjectively, and physiological variables were monitored. The TMA combination induced immobilisation with 1/7th of the TA thiafentanil dose and at a quarter of the cost. Induction times for the TA combination were significantly faster at 5.7 ± 1.6 min and more reliable compared to the TMA combination at 10.95 ± 3.9 min. Both combinations resulted in severe hypoxaemia, however hypoxaemia was overall more pronounced in the TMA (PaO2 44 ± 14 mmHg) combination compared to the TA (PaO2 51 ± 13,33 mmHg) combination and resulted mainly from decreased pulmonary oxygen exchange rather than hypoventilation; PaCO2 values were mostly within the normal expected physiological range. Supplementary oxygen and close monitoring of blood oxygenation is considered essential with either combination. Although the reduction in costs could be beneficial for the wildlife industry, longer induction times, and risks from severe hypoxaemia need to be taken into consideration when the TMA combination is used.
Comparison of three hematocrit measurement methods in the southern white rhinoceros (Ceratotherium simum simum)
(Wiley Periodicals LLC on behalf of American Society for Veterinary Clinical Pathology, 2022-06-01) Steyrer C; Pohlin F; Meyer LCR; Buss P; Hooijberg EH
Background: Hematocrit (HCT) determination is an integral part of health and disease assessments in captive and wild white rhinoceroses. Several affordable automated hematology analyzers have been developed for in-clinic and field use and have the advantage of being able to measure a large number of additional measurands. However, the accuracy of these analyzers for rhinoceros HCT measurements has not yet been investigated. Objectives: We aimed to compare the HCT results generated by the EPOC portable analyzer system and the Abaxis VetScan HM5 with the gold standard of a manual packed cell volume (PCV) measured using the microhematocrit method. Methods: Hematocrits were measured with the EPOC and the Abaxis VetScan HM5 (bovine setting) and compared with the PCVs of 69 white rhinoceros whole blood samples. Results were compared using Bland–Altman difference plots and Passing-Bablok regression analysis. A total allowable analytical error of 10% was set as the performance goal. Results: A significant positive bias, with a mean of 7.7% for the EPOC and 17.9% for the Abaxis, was found compared with the manual PCV method. Conclusions: The allowable error goal of 10% was not exceeded with the EPOC analyzer. Although not analytically equivalent to the gold standard, the EPOC results could therefore be used as approximations in critical situations where manual measurements cannot be performed. The Abaxis exceeded this allowable error and overestimated HCTs in rhinoceroses. Therefore, method-specific reference intervals should be used.
Conserving wildlife in a changing world: Understanding capture myopathy - A malignant outcome of stress during capture and translocation
(Oxford University Press on behalf of The Society for Experimental Biology, 2019-07-05) Breed D; Meyer LCR; Steyl JCA; Goddard A; Burroughs R; Kohn TA; Fuller A
The number of species that merit conservation interventions is increasing daily with ongoing habitat destruction, increased fragmentation and loss of population connectivity. Desertification and climate change reduce suitable conservation areas. Physiological stress is an inevitable part of the capture and translocation process of wild animals. Globally, capture myopathy - a malignant outcome of stress during capture operations - accounts for the highest number of deaths associated with wildlife translocation. These deaths may not only have considerable impacts on conservation efforts but also have direct and indirect financial implications. Such deaths usually are indicative of how well animal welfare was considered and addressed during a translocation exercise. Importantly, devastating consequences on the continued existence of threatened and endangered species succumbing to this known risk during capture and movement may result. Since first recorded in 1964 in Kenya, many cases of capture myopathy have been described, but the exact causes, pathophysiological mechanisms and treatment for this condition remain to be adequately studied and fully elucidated. Capture myopathy is a condition with marked morbidity and mortality that occur predominantly in wild animals around the globe. It arises from inflicted stress and physical exertion that would typically occur with prolonged or short intense pursuit, capture, restraint or transportation of wild animals. The condition carries a grave prognosis, and despite intensive extended and largely non-specific supportive treatment, the success rate is poor. Although not as common as in wildlife, domestic animals and humans are also affected by conditions with similar pathophysiology. This review aims to highlight the current state of knowledge related to the clinical and pathophysiological presentation, potential treatments, preventative measures and, importantly, the hypothetical causes and proposed pathomechanisms by comparing conditions found in domestic animals and humans. Future comparative strategies and research directions are proposed to help better understand the pathophysiology of capture myopathy.
Does cooling affect skeletal muscle glycogen replenishment after an acute bout of fear-induced exertional hyperthermia in blesbok (Damaliscus pygargus phillipsi)?
(Elsevier Inc, 2025-11-01) Kohn TA; Martin M; van Boom KM; Donaldson B; Blackhurst DM; Fitte A; Burroughs R; Steyl JCA; Goddard A; Meyer LCR
Rhabdomyolyses is a clinical sign of capture myopathy in wild animals and may be linked to glycogen metabolism. To study potential mechanisms, 26 wild blesbok were chased for 15 min and immobilised, whereafter 12 of these blesbok were doused with ice-water (n = 14 chased only group; n = 12 chased + cooled group). An additional 12 blesbok served as resting (not chased) uncooled controls. Vastus lateralis biopsies were obtained after immobilisation for biochemical analyses. Biopsies obtained at initial capture, 3- and 16-days post exercise were analysed for glycogen content. Blesbok muscles contained predominantly myosin heavy chain (MHC) IIA (∼50 ± 9 %), followed by IIX (32 ± 10 %) and MHC I (18 ± 5 %), with no difference between groups. Citrate synthase (mean: 87 ± 48), 3-hydroxyacetyl co A dehydrogenase (47 ± 17), lactate dehydrogenase (1567 ± 654), phosphorylase (162 ± 94), phosphofructokinase (250 ± 123) and creatine kinase (12,455 ± 6372) activities (in μmol/min/g prot) were not different between groups. Similarly, superoxide dismutase (7.9 ± 7 U/mg prot), catalase (8.8 ± 5.8 mmol/min/g prot), and overall antioxidant capacity (ORAC: 23055 ± 18,460 μmol/g prot) were not different between groups. Glycogen content was reduced in both chased groups and not replenished by day 3. Glycogen supercompensation was observed on day 16 in both chased groups (∼33 % higher than resting control group). The results confirm that blesbok have high muscle metabolic capacities, and that glycogen resynthesis is slow, which could lead to metabolite deficiency during prolonged chase events (>15 min).
Effects of three immobilizing drug combinations on ventilation, gas exchange and metabolism in free-living African lions (Panthera leo)
(Oxford University Press and the Society for Experimental Biology, 2023-08-10) Donaldson AC; Buss PE; Fuller A; Meyer LCR; Cooke SJ
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.
Efficacy and safety of three different opioid-based immobilisation combinations in blesbok (Damaliscus pygargus phillipsi)
(Medpharm Publications, 2023) Roug A; Smith C; Raath JP; Meyer LCR; Laubscher LL
African wildlife species are increasingly being immobilised with combinations of a low dose of potent opioids combined with medetomidine and azaperone. The physiological effects of these combinations in comparison to conventional potent opioid-azaperone combinations have scarcely been evaluated. In this cross-over study conducted on eight captive blesbok, we compared the physiological variables of blesbok immobilised with 2 mg of thiafentanil + 10 mg of azaperone (TA); 0.5 mg thiafentanil + 1.5 mg medetomidine (TM), and 0.5 mg thiafentanil + 1.5. mg medetomidine + 10 mg azaperone (TMA). Thiafentanil's effects were antagonised with naltrexone at 10 mg naltrexone per mg thiafentanil, and the medetomidine effects with atipamezole at 5 mg atipamezole per mg medetomidine. The physiological variables were compared between treatment groups using descriptive statistics and repeated measures ANOVA. The TA combination resulted in the shortest induction and recovery times, higher heart rates, respiratory rates, PaO2, SpO2, and lower MAP and A-a gradients, but with less muscle relaxation. The TM and TMA combinations caused marked bradycardia and hypoxaemia. The hypoxaemia was most severe in animals immobilised with TMA, and four of eight blesbok immobilised had a PaO2 < 35 mmHg at the 10- or 15-minute sampling point. These blesbok were provided supplementary oxygen, which corrected the hypoxaemia. The TA combinations caused the lowest degree of physiological compromise. All three combinations were effective for the immobilisation of blesbok, but as the low-dose thiafentanil and high-dose medetomidine combinations caused marked hypoxaemia, supplementary oxygen is recommended when using these combinations.
Etorphine induces pathophysiology in immobilized white rhinoceros through sympathomimesis that is attenuated by butorphanol
(y Oxford University Press and the Society for Experimental Biology, 2025-04-04) Boesch JM; Gleed RD; Buss PE; Tordiffe ASW; Zeiler GE; Miller MA; Viljoen F; Harvey BH; Parry SA; Meyer LCR; Madliger C
White rhinoceros are a sentinel species for important ecosystems in southern Africa. Their conservation requires active management of their population, which, in turn, requires immobilization of individuals with an ultra-potent opioid such as etorphine. Unfortunately, when immobilized with etorphine, they develop severe hypoxaemia that may contribute to morbidity and mortality. We hypothesized that (i) etorphine causes sympathetic upregulation that is responsible for physiological complications that produce hypoxaemia and (ii) butorphanol, a partial μ opioid agonist, mitigates sympathetic upregulation, thereby improving arterial oxygen content (CaO2) and delivery (DO2). Six subadult male white rhinoceros were administered two treatments in random order: etorphine-saline (ES) and etorphine-butorphanol (EB). After intramuscular etorphine (~2.6 μg kg−1), rhinoceros became recumbent (time 0 min [t0]) and were instrumented. Baseline data were collected at t30, butorphanol (0.026 mg/kg) or 0.9% saline was administered intravenously at t37, and data were collected again at t40 and t50. At baseline, plasma noradrenaline concentration was >40 ng ml−1, approximately twice that of non-immobilized rhinoceros (t test, P < 0.05); cardiac output (Qt, by thermodilution) and metabolic rate (VO2, by spirometry/indirect calorimetry) were greater than predicted allometrically (t test, P < 0.05), and pulmonary hypertension was present. After butorphanol, noradrenaline concentration remained greater than in non-immobilized rhinoceros; in EB, CaO2 was greater, while Qt, DO2, VO2, and pulmonary pressures were less than in ES (linear mixed effect model, all P < 0.05). Increased noradrenaline concentration with increased Qt and hypermetabolism supports etorphine-induced sympathetic upregulation. Butorphanol partly attenuated these effects, increasing CaO2 but reducing Qt and, thus, DO2. Since plasma noradrenaline concentration remained increased after butorphanol administration while Qt, DO2, and VO2 decreased, a pathway independent of plasma noradrenaline concentration might contribute to the cardiopulmonary and hypermetabolic effects of etorphine. Developing treatments to combat this sympathomimesis could reduce capture-related morbidity in white rhinoceros.
Evaluation of two different etorphine doses combined with azaperone in blesbok (damaliscus pygargus phillipsi) immobilisation
(South African Veterinary Association, 2021-12-09) Gaudio E; Laubscher LL; Meyer LCR; Hoffman LC; Raath JP; Pfitzer S
Chemical immobilisation is essential for veterinarians to perform medical procedures in wild African ungulates. Potent opioids combined with neuroleptic drugs are most often used for this purpose. The present study aimed at comparing the quality of immobilisation and effects on physiological variables between a high (high etorphine-azaperone [HE]: 0.09 mg kg-1) and low etorphine dose (low etorphine-azaperone [LE]: 0.05 mg kg-1), both combined with azaperone (0.35 mg kg-1), in 12 adult female boma-acclimatised blesbok. It was hypothesised that a reduction in etorphine's dose in combination with azaperone would result in less cardiorespiratory impairment but likely worsen the quality of immobilisation. Both treatments resulted in rapid induction and recovery times. Overall inter-treatment differences occurred in pulse rate (HE and LE: 52 ± 15 and 44 ± 11 beats minute-1, p < 0.0001), respiratory rate (HE and LE: 15 ± 4 and 17 ± 4 breaths minute-1, p < 0.006), partial pressure of exhaled carbon dioxide (HE and LE: 62.0 ± 5.0 and 60.0 ± 5.6 millimetre of mercury [mmHg], p < 0.028) and arterial carbon dioxide (HE and LE: 58.0 ± 4.5 and 55.0 ± 3.9 mmHg, p < 0.002). Both HE and LE led to bradycardia, hypertension and marked hypoxia to a similar extent. Furthermore, quality of induction, immobilisation and recovery were similar in both treatments. The role of azaperone in the development of cardiorespiratory compromise and gas exchange impairment that occurred when these combinations were used is still unclear. Further studies are recommended to elucidate drug- and dose-specific physiological effects in immobilised antelope.
Increased Diurnal Activity Is Indicative of Energy Deficit in a Nocturnal Mammal, the Aardvark
(Frontiers Media S.A., 2020-07-07) Weyer NM; Fuller A; Haw AJ; Meyer LCR; Mitchell D; Picker M; Rey B; Hetem RS; Nowack J
Shifting activity to cooler times of day buffers animals from increased heat and aridity under climate change. Conversely, when resources are limited, some nocturnal species become more diurnal, reducing energetic costs of keeping warm at night. Aardvarks (Orycteropus afer) are nocturnal, obligate ant- and termite-eating mammals which may be threatened directly by increasing heat and aridity, or indirectly by the effects of climate change on their prey. We hypothesised that the minimum 24-h body temperature of aardvarks would decline during energy scarcity, and that aardvarks would extend their active phases to compensate for reduced resource availability, possibly resulting in increased diurnal activity when aardvarks were energetically compromised. To measure their thermoregulatory patterns and foraging activity, we implanted abdominal temperature and activity data loggers into 12 adult aardvarks and observed them for varying durations over 3 years in the Kalahari. Under non-drought conditions, aardvarks tightly controlled their 24-h body temperature rhythm (mean amplitude of the 24-h body temperature rhythm was 1.8 ± 0.3°C during summer and 2.1 ± 0.1°C during winter) and usually were nocturnal. During a summer drought, aardvarks relaxed the precision of body temperature regulation (mean 24-h amplitude 2.3 ± 0.4°C) and those that subsequently died shifted their activity to progressively earlier times of day in the weeks before their deaths. Throughout the subsequent winter, the aardvarks’ minimum 24-h body temperatures declined, causing exaggerated heterothermy (4.7 ± 1.3°C; absolute range 24.7 to 38.8°C), with one individual’s body temperature varying by 11.7°C within 8 h. When body temperatures were low, aardvarks often emerged from burrows during daytime, and occasionally returned before sunset, resulting in completely diurnal activity. Aardvarks also shortened their active periods by 25% during food scarcity, likely to avoid energetic costs incurred by foraging. Despite their physiological and behavioural flexibility, aardvarks were unable to compensate for reduced food availability. Seven study aardvarks and several others died, presumably from starvation. Our results do not bode well for aardvarks facing climate change, and for the many animal species dependent on aardvark burrows for refuge.
Midazolam alters acid-base status less than azaperone during the capture and transport of southern white rhinoceroses (Ceratotherium simum simum)
(MDPI (Basel, Switzerland), 2020-07-31) Pohlin F; Buss P; Hooijberg EH; Meyer LCR
Acidemia represents a major life-threatening factor during rhinoceros capture. The acid-base status during rhinoceros transport is unknown. The purpose of this study was to describe changes in acid-base status during rhinoceros capture and transport and compare these changes between rhinoceroses sedated with azaperone or midazolam. Twenty-three wild white rhinoceros bulls were road-transported 280 km for reasons unrelated to this study. Rhinoceroses were captured with etorphine-azaperone (Group A) or etorphine-midazolam (Group M). During transport, azaperone (Group A) or midazolam (Group M) was re-administered every 2 h and venous blood collected. Changes in blood pH and associated variables were compared over time and between groups using a general linear mixed model. Rhinoceroses of both groups experienced a respiratory and metabolic acidosis during capture (pH 7.109 ± 0.099 and 7.196 ± 0.111 for Group A and Group M, respectively) that was quickly compensated for by the start of transport (pH 7.441 ± 0.035 and 7.430 ± 0.057) and remained stable throughout the journey. Rhinoceroses from Group M showed a smaller decrease in pH and associated variables at capture than rhinoceroses from Group A (p = 0.012). The use of midazolam instead of azaperone could therefore improve the success of rhinoceros capture and thus, contribute to the outcome of important conservation translocations.
Muscle tremors observed in white rhinoceroses immobilised with either etorphine-azaperone or etorphine-midazolam: An initial study
(AOSIS, 2021-06-28) Nasr M; Meyer LCR; Buss P; Fàbregas MC; Gleed RD; Boesch JM; Pohlin F
Etorphine-azaperone is the most commonly used drug combination for chemical immobilisation of free-ranging white rhinoceroses, but causes several profound physiological disturbances, including muscle tremors. The addition of benzodiazepine sedatives, such as midazolam, has been proposed to reduce the muscular rigidity and tremors in immobilised rhinoceroses. Twenty-three free-ranging, sub-adult white rhinoceros bulls were darted and captured using a combination of etorphine plus either azaperone or midazolam. Skeletal muscle tremors were visually evaluated and scored by an experienced veterinarian, and tremor scores and distance run were compared between groups using the Wilcoxon rank sum test. No statistical differences were observed in tremor scores (p = 0.435) or distance run (p = 0.711) between the two groups, and no correlation between these variables was detected (r = -0.628; p = 0.807). Etorphine-midazolam was as effective as etorphine-azaperone at immobilising rhinoceroses, with animals running similar distances. Although the addition of midazolam to the etorphine did not reduce tremor scores compared to azaperone, it might have other beneficial immobilising effects in rhinoceroses, and further investigation is necessary to elucidate possible methods of reducing muscle tremoring during chemical immobilisation of rhinoceroses.
Promoting rhinoceros welfare during transit: veterinarians' perspectives on transportation practices
(Medpharm Publications on behalf of the South African Veterinary Association, 2024-11-01) Macha ES; Meyer LCR; Leiberich M; Hofmeyr M; Hooijberg EH
Despite translocation being a useful conservation strategy in rhinoceros management, morbidities and mortalities occurring during transportation pose a significant concern to rhinoceros managers, veterinarians, and scientists. The objectives of this study were to better understand the effects of transport on rhinoceros and to gain insights from veterinarians involved in rhinoceros translocations about current practices and potential interventions that could improve welfare. A weblink and QR code to an online questionnaire with a total of 46 questions in Google Forms was sent to veterinarians who had experience in African rhinoceros transportation, through personal emails and social network forums. Results demonstrated that despite dehydration and negative energy balance being reported as the major causes of morbidities and mortalities during transport and post-release, most veterinarians (30/35; 86%) involved in rhinoceros translocation did not offer water, parenteral fluids, or feed to transported animals, for logistical reasons and the knowledge or perception of rhinoceros' resistance to taking ad lib food and water during transport. However, 52% (15/29) and 41% (15/34) of participants suggested that parenteral fluids could be used as an intervention to mitigate dehydration and negative energy balance respectively. To reduce stress, 94% (33/35) of respondents suggested the use of tranquilisers and sedatives. This study is the first to systematically investigate and report on practices by veterinarians involved in rhinoceros translocations globally. The study highlights that further research is required to explore optimal and pragmatic techniques in the field to mitigate reported welfare challenges in rhinoceros during transport.
Reference Intervals for Selected Hematology and Clinical Chemistry Measurands in Temminck's Pangolin (Smutsia temminckii)
(Frontiers Media S.A., 2021-07-08) Hooijberg EH; Lourens K; Meyer LCR; Viltrop A
Pangolins are the world’s most trafficked non-human mammals. A significant number of Temminck’s pangolins (Smutsia temminckii) are presented for veterinary care and rehabilitation in southern Africa. Little is known about the physiology and normal health of this species, making diagnosis and medical management difficult. This study aimed to establish reference intervals (RIs) for hematology and plasma clinical chemistry in the Temminck’s pangolin. RIs were generated according to international guidelines using samples from 27 healthy free-living (n = 18) and rehabilitated (n = 9) pangolins. Hematology was performed using the Abaxis VetScan HM5 analyzer with manual differentials; clinical chemistry was performed using heparin plasma on the Abaxis VetScan VS2 and Cobas Integra 400 Plus analyzers. Hematology RIs were: RBC 3.88–8.31 × 1012/L, HGB 73–150 g/L, HCT 26–51%, MCV 59–72 fL, MCH 15.6– 21.4 pg, MCHC 257–325 g/L, RDW 14.3–19.1%, WBC 1.80–10.71 × 109 /L. Vetscan VS2 clinical chemistry RIs were: albumin 27–41 g/L, ALP 26–100 U/L, ALT 25–307 U/L, amylase 267–826 U/L, bilirubin 4–10 µmol/L, calcium 2.1–2.2 mmol/L, globulin 21–55 g/L, glucose 3.8–10.0 mmol/L, phosphate 1.3–2.6 mmol/L, potassium 3.6–5.9 mmol/L, sodium 132–140 mmol/L total protein 52–84 g/L, and urea 5.3–11.4 mmol/L. RIs for creatinine were not calculated as analytical imprecision exceeded analytical performance goals. Cobas Integra clinical chemistry RIs were: albumin 22–33 g/L, ALP 20–104 U/L, ALT 17–291 U/L, amylase 466–1,533 U/L, bilirubin 1–14 µmol/L, calcium 2.0–2.4 mmol/L, creatinine

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