Laboratory of Pharmacology, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rodovia Araraquara-Jau Km 01 (Campus Universitário), Campus Ville, 14800-903 Araraquara, SP, Brazil; Joint UFSCar-UNESP Graduate Program in Physiological Sciences, São Carlos, SP, Brazil.
Laboratory of Pharmacology, School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rodovia Araraquara-Jau Km 01 (Campus Universitário), Campus Ville, 14800-903 Araraquara, SP, Brazil; Joint UFSCar-UNESP Graduate Program in Physiological Sciences, São Carlos, SP, Brazil.
Eur Neuropsychopharmacol. 2019 May;29(5):672-680. doi: 10.1016/j.euroneuro.2019.03.001. Epub 2019 Mar 14.
The lateral hypothalamus (LH) has been described as one of the hypothalamic areas involved in the behavioral and physiological responses triggered by aversive stimuli. Previous studies indicated involvement of the LH in cardiovascular responses to stress. Despite this evidence, the local neurochemical mechanisms involved in LH control of stress responses is still poorly understood. Therefore, in the present study, we investigated the role of GABAergic neurotransmission within the LH in cardiovascular responses induced by an acute session of restraint stress in rats. For this, we evaluated the effect of bilateral microinjection of selective antagonists of either GABA or GABA receptors into the LH on arterial pressure increase, heart rate (HR) increase and reduction in tail skin temperature induced by restraint stress. We found that microinjection of the selective GABA receptor antagonist SR95531 into the LH decreased the increase in HR caused by restraint stress, but without affecting the increase in arterial pressure increase or the reduction in tail skin temperature. Conversely, LH treatment with the selective GABA receptor antagonist CGP35348 did not affect the restraint-evoked cardiovascular changes. These findings indicate that GABAergic neurotransmission in the LH, acting through activation of local GABA receptors, plays a facilitatory role in the tachycardic response observed during aversive threats.
外侧下丘脑(LH)已被描述为参与厌恶刺激引发的行为和生理反应的下丘脑区域之一。先前的研究表明 LH 参与了应激的心血管反应。尽管有这些证据,但 LH 控制应激反应的局部神经化学机制仍知之甚少。因此,在本研究中,我们研究了 LH 内 GABA 能神经传递在大鼠急性束缚应激诱导的心血管反应中的作用。为此,我们评估了将选择性 GABA 或 GABA 受体拮抗剂双侧微注射到 LH 中对束缚应激引起的动脉压升高、心率(HR)升高和尾巴皮肤温度降低的影响。我们发现,将选择性 GABA 受体拮抗剂 SR95531 微注射到 LH 中可降低束缚应激引起的 HR 升高,但不影响动脉压升高或尾巴皮肤温度降低。相反,LH 用选择性 GABA 受体拮抗剂 CGP35348 处理并未影响束缚引起的心血管变化。这些发现表明,LH 中的 GABA 能神经传递通过激活局部 GABA 受体,在厌恶威胁期间观察到的心动过速反应中发挥促进作用。