Taugher Rebecca J, Ghobbeh Ali, Sowers Levi P, Fan Rong, Wemmie John A
Department of Psychiatry, University of Iowa Iowa City, IA, USA ; Department of Veterans Affairs Medical Center Iowa City, IA, USA.
Department of Veterans Affairs Medical Center Iowa City, IA, USA ; Department of Molecular Physiology and Biophysics, University of Iowa Iowa City, IA, USA.
Front Neurosci. 2015 Jul 21;9:239. doi: 10.3389/fnins.2015.00239. eCollection 2015.
Mice display an unconditioned freezing response to TMT, a predator odor isolated from fox feces. Here we found that in addition to freezing, TMT caused mice to decrease breathing rate, perhaps because of the aversive smell. Consistent with this possibility, olfactory bulb lesions attenuated this effect of TMT, as well as freezing. Interestingly, butyric acid, another foul odor, also caused mice to reduce breathing rate. However, unlike TMT, butyric acid did not induce freezing. Thus, although these aversive odors may affect breathing, the unpleasant smell and suppression of breathing by themselves are insufficient to cause freezing. Because the acid-sensing ion channel-1A (ASIC1A) has been previously implicated in TMT-evoked freezing, we tested whether Asic1a disruption also altered breathing. We found that TMT reduced breathing rate in both Asic1a(+/+) and Asic1a(-/-) mice, suggesting that ASIC1A is not required for TMT to inhibit breathing and that the absence of TMT-evoked freezing in the Asic1a(-/-) mice is not due to an inability to detect TMT. These observations further indicate that ASIC1A must affect TMT freezing in another way. Because the bed nucleus of the stria terminalis (BNST) has been critically implicated in TMT-evoked freezing and robustly expresses ASIC1A, we tested whether ASIC1A in the BNST plays a role in TMT-evoked freezing. We disrupted ASIC1A in the BNST of Asic1a(loxP/loxP) mice by delivering Cre recombinase to the BNST with an adeno-associated virus (AAV) vector. We found that disrupting ASIC1A in the BNST reduced TMT-evoked freezing relative to control mice in which a virus expressing eGFP was injected. To test whether ASIC1A in the BNST was sufficient to increase TMT-evoked freezing, we used another AAV vector to express ASIC1A in the BNST of Asic1a(-/-) mice. We found region-restricted expression of ASIC1A in the BNST increased TMT-elicited freezing. Together, these data suggest that the BNST is a key site of ASIC1A action in TMT-evoked freezing.
小鼠对TMT(一种从狐狸粪便中分离出的捕食者气味)会表现出无条件的僵住反应。我们发现,除了僵住外,TMT还会使小鼠呼吸频率降低,这可能是由于厌恶气味所致。与这种可能性一致的是,嗅球损伤减弱了TMT的这种作用以及僵住反应。有趣的是,另一种恶臭丁酸也会使小鼠呼吸频率降低。然而,与TMT不同的是,丁酸不会诱发僵住。因此,尽管这些厌恶气味可能会影响呼吸,但难闻的气味和呼吸抑制本身不足以导致僵住。由于酸敏感离子通道1A(ASIC1A)先前被认为与TMT诱发的僵住有关,我们测试了Asic1a基因敲除是否也会改变呼吸。我们发现,TMT会降低Asic1a(+/+)和Asic1a(-/-)小鼠的呼吸频率,这表明TMT抑制呼吸并不需要ASIC1A,且Asic1a(-/-)小鼠中缺乏TMT诱发的僵住并非由于无法检测到TMT。这些观察结果进一步表明,ASIC1A必定以另一种方式影响TMT诱发的僵住。由于终纹床核(BNST)在TMT诱发的僵住中起关键作用且大量表达ASIC1A,我们测试了BNST中的ASIC1A在TMT诱发的僵住中是否起作用。我们通过腺相关病毒(AAV)载体将Cre重组酶导入Asic1a(loxP/loxP)小鼠的BNST中,从而敲除BNST中的ASIC1A。我们发现,与注射表达绿色荧光蛋白(eGFP)病毒的对照小鼠相比,敲除BNST中的ASIC1A会降低TMT诱发的僵住。为了测试BNST中的ASIC1A是否足以增加TMT诱发的僵住,我们使用另一种AAV载体在Asic1a(-/-)小鼠的BNST中表达ASIC1A。我们发现,BNST中ASIC1A的区域限制性表达增加了TMT诱发的僵住。总之,这些数据表明,BNST是ASIC1A在TMT诱发僵住中发挥作用的关键部位。