Guner Ibrahim, Sahin Gulderen, Yelmen Nermin Karaturan, Aksu Ugur, Oruc Tulin, Yildirim Zeynep
Istanbul University, Cerrahpasa Faculty of Medicine, Department of Physiology, Istanbul, Turkey.
Chin J Physiol. 2008 Jun 30;51(3):136-45.
Hypoxia causes changes in the rate of synthesis or release of neurotransmitters in the brain. The accumulation of serotonin (5-HT) in the central nervous system might cause hypoxic respiratory depression. In the present study, we aimed to examine the role of central 5-HT on normoxic and acute hypoxic ventilatory depression (AHVD) in peripheral chemoreceptors denervated rabbits. All experiments were performed in peripherally chemodenervated rabbits anesthetized with intravenous injection of urethane (400 mg/kg) and alpha-chloralose (40 mg/kg). For intracerebroventricular (ICV) administration of 5-HT (20 microg/kg) and ketanserin (10 microg/kg), a cannula was placed in left lateral ventricle by stereotaxic method. Respiratory frequency (fR), tidal volume (VT), ventilation minute volume (VE) and systemic arterial bood pressure (BP) were recorded in each experimental phases and mean arterial pressure was calculated (MAP). Heart rate (HR) was also determined from the pulsation of BP. The effects of ICV serotonin and ICV ketanserin on the indicated parameters during air breathing (normoxia) and breathing of hypoxia (8% O2--92% N2) were investigated. During hypoxia, fR, VT, VE, MAP and HR decreased, and AHVD was thus obtained. ICV injection of 5-HT during normoxia caused significant increases in VT (P < 0.001) and in VE (P < 0.01). On the other hand, ICV 5-HT injection reduced the degree of AHVD in peripherally chemodenervated rabbits during hypoxia (fR; P < 0.05, VT; P < 0.05 and VE; P < 0.01). After ICV injection of ketanserin, the enhancement of 5-HT on VE was prevented during normoxia. On the breathing of hypoxic gas after ICV ketanserin, the degree of AHVD was augmented. In conclusion, our findings suggested that central 5-HT increases normoxic ventilation and reduces the degree of AHVD during hypoxia and that ICV ketanserin prevents the stimulatory effect of 5-HT on respiration and augments AHVD.
缺氧会导致大脑中神经递质合成或释放速率的改变。血清素(5-羟色胺,5-HT)在中枢神经系统中的蓄积可能会导致缺氧性呼吸抑制。在本研究中,我们旨在探讨中枢5-HT在去神经支配外周化学感受器的家兔常氧和急性缺氧性通气抑制(AHVD)中的作用。所有实验均在静脉注射氨基甲酸乙酯(400 mg/kg)和α-氯醛糖(40 mg/kg)麻醉的去神经支配外周化学感受器的家兔身上进行。为了脑室内(ICV)注射5-HT(20 μg/kg)和酮色林(10 μg/kg),通过立体定位法将套管置于左侧脑室。在每个实验阶段记录呼吸频率(fR)、潮气量(VT)、分钟通气量(VE)和体循环动脉血压(BP),并计算平均动脉压(MAP)。心率(HR)也通过血压搏动来确定。研究了ICV注射血清素和ICV注射酮色林对常氧呼吸(常氧)和缺氧呼吸(8% O₂ - 92% N₂)期间上述参数的影响。在缺氧期间,fR、VT、VE、MAP和HR下降,从而获得AHVD。常氧期间ICV注射5-HT导致VT(P < 0.001)和VE(P < 0.01)显著增加。另一方面,ICV注射5-HT可降低缺氧期间去神经支配外周化学感受器家兔的AHVD程度(fR;P < 0.05,VT;P < 0.05,VE;P < 0.01)。ICV注射酮色林后,常氧期间5-HT对VE的增强作用被阻断。ICV注射酮色林后在缺氧气体呼吸时,AHVD程度增加。总之,我们的研究结果表明,中枢5-HT可增加常氧通气并降低缺氧期间的AHVD程度,并且ICV注射酮色林可阻断5-HT对呼吸的刺激作用并增强AHVD。