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1.
Ecol Evol ; 14(6): e11455, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38855312

RESUMO

Climate change is predicted to narrow the prescriptive zone of dryland species, potentially leading to behavioural modifications with fitness consequences. This study explores the behavioural responses of three widespread African antelope species-springbok, kudu and eland-to extreme heat in a dryland savanna. We classified the behaviour of 29 individuals during the hot, dry season on the basis of accelerometer data using supervised machine learning and analysed the impact of afternoon heat on behaviour-specific time allocation and overall dynamic body acceleration (ODBA), a proxy for energy expenditure, along with compensatory changes over the 24-hour cycle. Extreme afternoon heat reduced feeding time in all three antelope species, increased ruminating and resting time, while only minimally affecting walking time. With rising heat, all three species reduced ODBA on feeding, while eland reduced and kudu increased ODBA on walking. Diel responses in behaviour differed between species, but were generally characterised by daytime reductions in feeding and increases in ruminating or resting on hot days compared to cool days. While antelope compensated for heat-driven behavioural change over the 24-hour cycle in some cases, significant differences persisted in others, including reduced feeding and increased rumination and resting. The impact of heat on antelope behaviour reveals trade-offs between feeding and thermoregulation, as well as between feeding and rumination, the latter suggesting a strategy to enhance nutrient uptake through increased digestive efficiency, while the walking response suggests narrow constraints between cost and necessity. Our findings suggest that heat influences both behaviour-specific time allocation and energy expenditure. Altered diel behaviour patterns and incomplete compensation over the 24-hour cycle point to fitness consequences. The need to prioritise thermoregulation over feeding is likely to narrow the prescriptive zone of these dryland antelope.

2.
Addiction ; 114(8): 1416-1426, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-31013390

RESUMO

AIMS: To assess the long-term safety of subcutaneous buprenorphine (CAM2038) weekly and monthly depots. DESIGN: Phase 3, open-label, observational, multi-centre 48-week trial (ClinicalTrials.gov NCT02672111). SETTING: Twenty-six out-patient sites (United States, United Kingdom, Hungary, Denmark, Sweden, Germany, Australia) between 14 December 2015 and 12 April 2017. PARTICIPANTS: Two hundred and twenty-eight adults with opioid use disorder; 227 received CAM2038 (37 initiated onto CAM2038 and 190 converted from sublingual buprenorphine). INTERVENTIONS: CAM2038 weekly (8, 16, 24 or 32 mg) or monthly (64, 96, 128 or 160 mg) with flexible dosing and individualized titration utilizing multiple CAM2038 weekly and monthly doses. MEASUREMENTS: Safety variables, urine toxicology samples and self-reported illicit opioid use were collected at each visit. Participants were administered a patient satisfaction survey at months 6 and 12, completed by 162 of 227 (71.4%) participants. FINDINGS: The study treatment period was completed by 167 of 227 (73.6%) participants. At least one treatment-emergent adverse event (TEAE) was reported by 143 of 227 (63.0%) participants, of whom 60 of 227 (26.4%) reported as being drug-related. Most of the TEAEs, reported by 128 of 227 (56.4%) of participants, were mild or moderate in intensity. Injection-site reactions were reported by 46 of 227 (20.3%) participants, with most [45 of 46 (97.8%)] reported as mild to moderate. Five participants (2.2%) discontinued the study drug due to a TEAE, two cases (0.9%) of which were injection-site-related. No serious adverse events were attributed to the study drug. Among those remaining in the study, the percentage of opioid-negative urine tests combined with self-reports was 63.0% (17 of 27) in new-to-treatment participants and 82.8% (111 of 134) for those converted from sublingual buprenorphine. Participants reported high levels of satisfaction with CAM2038. CONCLUSIONS: Subcutaneous buprenorphine delivered weekly or monthly (CAM2038) was well tolerated, with a systemic safety profile consistent with the known profile of sublingual buprenorphine. CAM2038 weekly and monthly was associated with high retention rates and low levels of illicit opioid use throughout this study.


Assuntos
Analgésicos Opioides/administração & dosagem , Buprenorfina/administração & dosagem , Preparações de Ação Retardada/administração & dosagem , Antagonistas de Entorpecentes/administração & dosagem , Transtornos Relacionados ao Uso de Opioides/tratamento farmacológico , Adulto , Idoso , Austrália , Dinamarca , Monitoramento de Medicamentos , Feminino , Alemanha , Humanos , Hungria , Injeções Subcutâneas , Masculino , Pessoa de Meia-Idade , Pacientes Ambulatoriais/psicologia , Segurança do Paciente , Satisfação do Paciente , Suécia , Reino Unido , Estados Unidos
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