Xu Changqing, Seubert Christoph N, Gravenstein Nikolaus, Martynyuk Anatoly E
Department of Anesthesiology, University of Florida College of Medicine, Gainesville, FL, United States.
Department of Anesthesiology, University of Florida College of Medicine, Gainesville, FL, United States; McKnight Brain Institute, University of Florida College of Medicine, Gainesville, FL, United States.
Neurosci Lett. 2016 Apr 8;618:1-5. doi: 10.1016/j.neulet.2016.02.045. Epub 2016 Feb 26.
Animal studies provide strong evidence that general anesthetics (GAs), administered during the early postnatal period, induce long-term cognitive and neurological abnormalities. Because the brain growth spurt in rodents is delayed compared to that in humans, a fundamental question is whether the postnatal human brain is similarly vulnerable. Sevoflurane and propofol, GAs that share positive modulation of the gamma-aminobutyric acid type A receptor (GABAAR) function cause marked increase in corticosterone levels and induce long-term developmental alterations in synaptic activity in rodents. If synaptogenesis is affected, investigation of mechanisms of the synaptic effects of GAs is of high interest because synaptogenesis in humans continues for several years after birth. Here, we compared long-term synaptic effects of etomidate with those of propofol. Etomidate and propofol both positively modulate GABAAR activity, but in contrast to propofol, etomidate inhibits the adrenal synthesis of corticosterone. Postnatal day (P) 4, 5, or 6 rats received five injections of etomidate, propofol, or vehicle control during 5h of maternal separation. Endocrine effects of the anesthetics were evaluated by measuring serum levels of corticosterone immediately after anesthesia or maternal separation. The frequency and amplitude of miniature inhibitory postsynaptic currents (mIPSCs) in hippocampal CA1 pyramidal neurons were measured at P24-40 and P≥80. Only propofol caused a significant increase in serum corticosterone levels (F(4.26)=17.739, P<0.001). In contrast to increased frequency of mIPSCs in the propofol group (F(4.23)=8.731, p<0.001), mIPSC activity in the etomidate group was not different from that in the vehicle groups. The results of this study together with previously published data suggest that anesthetic-caused increase in corticosterone levels is required for GABAergic GAs to induce synaptic effects in the form of a long-term increase in the frequency of hippocampal mIPSCs.
动物研究提供了有力证据,表明在出生后早期给予全身麻醉药(GAs)会诱发长期的认知和神经异常。由于与人类相比,啮齿动物的脑发育激增有所延迟,一个根本问题是出生后的人类大脑是否同样脆弱。七氟醚和丙泊酚这两种全身麻醉药对A型γ-氨基丁酸受体(GABAAR)功能具有正向调节作用,会导致皮质酮水平显著升高,并在啮齿动物中诱发突触活动的长期发育改变。如果突触形成受到影响,那么对全身麻醉药突触效应机制的研究就会备受关注,因为人类的突触形成在出生后会持续数年。在此,我们比较了依托咪酯和丙泊酚的长期突触效应。依托咪酯和丙泊酚都能正向调节GABAAR活性,但与丙泊酚不同的是,依托咪酯会抑制肾上腺皮质酮的合成。出生后第(P)4、5或6天的大鼠在母体分离的5小时内接受了五次依托咪酯、丙泊酚或溶剂对照注射。通过在麻醉或母体分离后立即测量血清皮质酮水平来评估麻醉药的内分泌效应。在P24 - 40和P≥80时测量海马CA1锥体神经元中微小抑制性突触后电流(mIPSCs)的频率和幅度。只有丙泊酚导致血清皮质酮水平显著升高(F(4.26)=17.739,P<0.001)。与丙泊酚组mIPSCs频率增加相反(F(4.23)=·8.731,p<0.001),依托咪酯组的mIPSC活性与溶剂组没有差异。这项研究的结果与先前发表的数据共同表明,GABA能全身麻醉药要以海马mIPSCs频率长期增加的形式诱发突触效应,则需要麻醉药导致皮质酮水平升高。