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胍法辛在两只长尾猕猴中介导焦虑相关反应和减少相关激进行为的应用。

The Use of Guanfacine to Mediate Anxiety-related Reactivity and Reduce Associated Agonistic Behavior in Two Pigtail Macaques ().

机构信息

Department of Molecular and Comparative Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland; Research Animal Resources, Johns Hopkins University, Baltimore, Maryland.

Research Animal Resources, Johns Hopkins University, Baltimore, Maryland.

出版信息

Comp Med. 2024 Jun 1;74(3):186-194. doi: 10.30802/AALAS-CM-24-000001. Epub 2024 Apr 10.

DOI:10.30802/AALAS-CM-24-000001
PMID:38599780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11267446/
Abstract

Guanfacine, an α ₂adrenoceptor agonist, has been used to successfully treat self-injurious behavior in nonhuman primates, including macaques () and baboons (). It does so by facilitating a correction to the dopaminergic system that mediates a reduction in impulsivity and reactivity. Given this, we assessed the potential efficacy of guanfacine to treat socially directed agonistic behavior in primates with an apparent reactive behavioral phenotype. We present data from 2 pigtail macaques (): an intact adult male housed in a breeding group, and an experimentally naive adult female living in a research setting with her social partner. Baseline behavioral assessments suggested that both macaques showed extreme responses to external stressors that triggered them to aggress social partners often leading to wounding that required veterinary intervention. Both animals were tracked during the course of 1 y. Once treated regularly with guanfacine, both animals showed significant reduction in their agonistic behavior and the rate at which they wounded other animals. Indeed, in the year since the female has been treated with guanfacine she has never wounded her cagemate. By collecting regular and detailed behavioral observations on the male in the breeding colony, we were able to identify triggers for his aggression and to track the behavioral changes evidenced after guanfacine treatment. These data supported our hypothesis that his aggression reflected extreme reactivity to external stressors, rather than general anxiety. Importantly, we saw only a limited and short-lived reduction in the male's affiliative behavioral rates, and thus guanfacine had no sedative effect, but did successfully reduce his reactivity and resultant agonism and wounding.

摘要

胍法辛是一种 α2 肾上腺素受体激动剂,已成功用于治疗非人类灵长类动物的自伤行为,包括猕猴()和狒狒()。它通过促进介导冲动性和反应性降低的多巴胺能系统的校正来实现这一点。有鉴于此,我们评估了胍法辛治疗具有明显反应性行为表型的灵长类动物社交定向攻击行为的潜在疗效。我们提出了来自 2 只长尾猕猴的数据():一只生活在繁殖群体中的健全成年雄性,以及一只生活在研究环境中与其社交伙伴在一起的实验性新生成年雌性。基线行为评估表明,两只猕猴对触发它们攻击社交伙伴的外部压力源都表现出极端反应,这常常导致需要兽医干预的伤口。在 1 年的时间里,这两只动物都被跟踪观察。一旦定期用胍法辛治疗,两只动物的攻击性行为及其伤害其他动物的速度都明显减少。事实上,自从雌性接受胍法辛治疗以来,她从未伤害过她的笼伴。通过对繁殖群中的雄性进行定期和详细的行为观察,我们能够确定他攻击的触发因素,并跟踪胍法辛治疗后表现出的行为变化。这些数据支持了我们的假设,即他的攻击反映了对外部压力源的极端反应性,而不是一般的焦虑。重要的是,我们只看到雄性的亲社会行为率有有限的短暂减少,因此胍法辛没有镇静作用,但确实成功地降低了他的反应性和由此产生的攻击性行为和伤口。