首页> 外文期刊>JAMA otolaryngology-- head & neck surgery >Establishment of a rabbit model of obstructive sleep apnea by paralyzing the genioglossus.
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Establishment of a rabbit model of obstructive sleep apnea by paralyzing the genioglossus.

机译:通过使舌肌麻痹建立阻塞性睡眠呼吸暂停兔模型。

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IMPORTANCE This study presents an innovative method for developing a neuromuscular model of obstructive sleep apnea (OSA). OBJECTIVE To establish a new OSA animal model simulating real upper airway conditions during sleep. DESIGN AND SETTING In vivo animal study at an academic tertiary referral center. SUBJECTS A total of 27 New Zealand white male rabbits were used. INTERVENTION Sleep was induced by intramuscular injection of 0.3 mL/kg of tiletamine hydrochloride plus zolazepam hydrochloride and 0.2 mL/kg of xylazine. Upper airway obstruction was induced by injecting botulinum toxin type A (2.5 U in 8 rabbits, 5.0 U in 10 rabbits, and 7.5 U in 1 rabbit) into the genioglossus. Eight rabbits were injected with normal saline as a control. MAIN OUTCOMES AND MEASURES Drug-induced sleep was evaluated using a portable polysomnography device for electroencephalography, electrooculography, chin electromyography, nasal airflow, breathing efforts, and pulse oxymetry. Respiratory events (apneas or hypopneas) during sleep were evaluated using a sleep-screening tool. RESULTS All the rabbits showed no apneas or hypopneas before injection of botulinum toxin type A. In the control rabbits injected with normal saline, apneas or hypopneas were not found. The respiratory events were observed in 5 of 8 rabbits injected with 2.5 U of botulinum toxin type A, whereas they were observed in 7 of 10 rabbits injected with 5.0 U of botulinum toxin type A. The median (interquartile range) apnea hypopnea index was 9.6 (5.3-14.8) per hour and 45.6 (21.5-70.5) per hour in the rabbits injected with 2.5 U and 5.0 U of botulinum toxin type A, respectively (P?=?.03). CONCLUSIONS AND RELEVANCE An animal model of OSA could be developed by paralyzing the genioglossus in rabbits. This model may contribute to identifying the pathogenesis of upper airway obstruction in OSA and to developing new diagnostic or treatment devices targeting specific obstruction sites.
机译:重要性本研究提出了一种创新的方法,用于开发阻塞性睡眠呼吸暂停(OSA)的神经肌肉模型。目的建立一种新的OSA动物模型,以模拟睡眠中真实的上呼吸道状况。设计与设置在大学第三级转诊中心进行的体内动物研究。受试者共使用27只新西兰白公兔。干预通过肌内注射0.3 mL / kg的盐酸维他命胺加盐酸左唑西am和0.2 mL / kg的甲苯噻嗪诱导睡眠。通过向A舌肌注射A型肉毒杆菌毒素(8只兔2.5 U,10只兔5.0 U,1只兔7.5 U)诱导上呼吸道阻塞。八只兔子注射生理盐水作为对照。主要结果和措施使用便携式多导睡眠图仪评估药物诱发的睡眠,该仪用于脑电图,眼电图,下巴肌电图,鼻气流,呼吸努力和脉搏血氧仪。使用睡眠筛查工具评估睡眠期间的呼吸事件(呼吸暂停或呼吸不足)。结果所有兔子在注射A型肉毒杆菌毒素之前均未显示出呼吸暂停或呼吸不足。在注射生理盐水的对照组中,未发现呼吸暂停或呼吸不足。注射2.5 U A型肉毒杆菌毒素的8只兔中有5只观察到呼吸事件,而注射5.0 U A型肉毒杆菌毒素的10只兔中有7只观察到呼吸事件。呼吸暂停低通气指数的中位数(四分位间距)为9.6在分别注射了2.5 U和5.0 U A型肉毒杆菌毒素的兔子中,每小时(5.3-14.8)每小时和45.6(21.5-70.5)每小时(P?= ?. 03)。结论和相关性可以通过使家兔的舌s瘫痪来建立OSA的动物模型。该模型可能有助于确定OSA中上呼吸道阻塞的发病机理,并有助于开发针对特定阻塞部位的新型诊断或治疗设备。

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