Bussey Carol T, de Leeuw Anne E, Lamberts Regis R
HeartOtago, Department of Physiology, Otago School of Medical Sciences, University of Otago, Dunedin 9054, New Zealand.
Cardiovasc Diabetol. 2014 Dec 10;13:161. doi: 10.1186/s12933-014-0161-4.
Increasing numbers of type 2 diabetic and obese patients with enhanced rates of cardiovascular complications require surgical interventions, however they have a higher incidence of perioperative haemodynamic complications, which has been linked to adrenergic dysfunction. Therefore, we aimed to determine how α- and β-adrenoceptor (AR)-mediated haemodynamic responses are affected by isoflurane anaesthesia in experimental type 2 diabetes and obesity in vivo.
Sixteen-week old male Zucker type 2 Diabetic Fatty (ZDF) rats, Zucker Obese rats and their lean counterparts (n = 7-9 per group) were instrumented with radio telemeters to record blood pressure and heart rate and with vascular access ports for non-invasive intravenous drug delivery in vivo. Haemodynamic effects of α-AR (phenylephrine; 1-100 μg x kg(-1)) or β-AR (dobutamine; 2-120 μg x kg(-1)) stimulation were assessed under conscious and anaesthetised (isoflurane; 2%) conditions.
Vascular α-AR sensitivity was increased in both diabetic (non-diabetic 80 ± 3 vs. diabetic 95 ± 4 ΔmmHg at 100 μg x kg(-1); p < 0.05) and obese (lean 65 ± 6 vs. obese 84 ± 6 ΔmmHg at 20 μg x kg(-1); p < 0.05) conscious rats. Interestingly, anaesthesia exacerbated and prolonged the increased α-AR function in both diabetic and obese animals (non-diabetic 51 ± 1 vs. diabetic 68 ± 4 ΔmmHg, lean 61 ± 5 vs. obese 84 ± 2 ΔmmHg at 20 μg x kg(-1); p < 0.05). Meanwhile, β-AR chronotropic sensitivity was reduced in conscious diabetic and obese rats (non-diabetic 58 ± 7 vs. diabetic 27 ± 8 Δbpm, lean 103 ± 12 vs. obese 61 ± 9 Δbpm at 15 μg x kg(-1); p < 0.05). Anaesthesia normalised chronotropic β-AR responses, via either a limited reduction in obese (lean 51 ± 3 vs. obese 66 ± 5 Δbpm; NS at 15 μg x kg(-1)) or increased responses in diabetic animals (non-diabetic 49 ± 8 vs. diabetic 63 ± 8 Δbpm, at 15 μg x kg(-1); NS at 15 μg x kg(-1)).
Long term metabolic stress, such as during type 2 diabetes and obesity, alters α- and β-AR function, its dynamics and the interaction with isoflurane anaesthesia. During anaesthesia, enhanced α-AR sensitivity and normalised β-AR function may impair cardiovascular function in experimental type 2 diabetes and obesity.
越来越多的2型糖尿病和肥胖患者心血管并发症发生率增加,需要手术干预,然而他们围手术期血流动力学并发症的发生率较高,这与肾上腺素能功能障碍有关。因此,我们旨在确定在实验性2型糖尿病和肥胖的体内,异氟烷麻醉如何影响α和β肾上腺素能受体(AR)介导的血流动力学反应。
16周龄雄性Zucker 2型糖尿病肥胖(ZDF)大鼠、Zucker肥胖大鼠及其瘦型对照大鼠(每组n = 7 - 9)植入无线电遥测仪以记录血压和心率,并植入血管通路端口以便在体内进行非侵入性静脉给药。在清醒和麻醉(异氟烷;2%)条件下评估α-AR(去氧肾上腺素;1 - 100 μg x kg(-1))或β-AR(多巴酚丁胺;2 - 120 μg x kg(-1))刺激的血流动力学效应。
在清醒的糖尿病(非糖尿病组在100 μg x kg(-1)时为80 ± 3 vs. 糖尿病组为95 ± 4 ΔmmHg;p < 0.05)和肥胖(瘦型组在20 μg x kg(-1)时为65 ± 6 vs. 肥胖组为84 ± 6 ΔmmHg;p < 0.05)大鼠中,血管α-AR敏感性均增加。有趣的是,麻醉加剧并延长了糖尿病和肥胖动物中α-AR功能的增加(非糖尿病组在20 μg x kg(-1)时为51 ± 1 vs. 糖尿病组为68 ± 4 ΔmmHg,瘦型组为61 ± 5 vs. 肥胖组为84 ± 2 ΔmmHg;p < 0.05)。同时,清醒的糖尿病和肥胖大鼠中β-AR变时敏感性降低(非糖尿病组在15 μg x kg(-1)时为58 ± 7 vs. 糖尿病组为27 ± 8 Δbpm,瘦型组为103 ± 12 vs. 肥胖组为61 ± 9 Δbpm;p < 0.05)。麻醉使变时β-AR反应正常化,在肥胖动物中通过有限降低(瘦型组在15 μg x kg(-1)时为51 ± 3 vs. 肥胖组为66 ± 5 Δbpm;无统计学差异),在糖尿病动物中通过增加反应(非糖尿病组在15 μg x kg(-1)时为49 ± 8 vs. 糖尿病组为63 ± 8 Δbpm,在15 μg x kg(-1)时;无统计学差异)。
长期代谢应激,如在2型糖尿病和肥胖期间,会改变α和β-AR功能、其动力学以及与异氟烷麻醉的相互作用。在麻醉期间,增强的α-AR敏感性和正常化的β-AR功能可能损害实验性2型糖尿病和肥胖中的心血管功能。