ASIC1A in the bed nucleus of the stria terminalis mediates TMT-evoked freezing

被引:11
作者
Taugher, Rebecca J. [1 ,2 ]
Ghobbeh, Ali [1 ,2 ]
Sowers, Levi P. [2 ,3 ]
Fan, Rong [1 ,2 ]
Wemmie, John A. [1 ,2 ,3 ]
机构
[1] Univ Iowa, Dept Psychiat, Iowa City, IA 52242 USA
[2] Dept Vet Affairs Med Ctr, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
关键词
TMT; bed nucleus of the stria terminalis; ASIC1A; respiratory rate; predator odor; PREDATOR ODOR; FOX ODOR; TRIMETHYLTHIAZOLINE TMT; TEMPORARY INACTIVATION; SYNAPTIC PLASTICITY; UNCONDITIONED FEAR; AMYGDALA; ACID; BEHAVIOR; COMPONENT;
D O I
10.3389/fnins.2015.00239
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 Asicla 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 ASIC1 A 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.
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页数:7
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