Abstract

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 Asic1aloxP/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.

Highlights

  • Exposure to odors from predators, such as foxes and cats, can elicit unconditioned freezing and avoidance responses in rodents (Takahashi et al, 2005)

  • Because a recent study in rats found that olfactory bulb lesions eliminated TMT-evoked freezing (Ayers et al, 2013), we wondered whether TMT effects on breathing rate might depend on the olfactory bulb

  • We found that olfactory bulb lesions significantly attenuated effects of TMT on breathing rate (Figure 1B), as well as freezing (Figure 1C)

Read more

Summary

Introduction

Exposure to odors from predators, such as foxes and cats, can elicit unconditioned freezing and avoidance responses in rodents (Takahashi et al, 2005). TMT evokes freezing and avoidance responses in rodents (Vernet-Maury et al, 1984; Fendt et al, 2003). Because this freezing is seen even in naïve animals raised in the laboratory setting, TMT is thought to be an unconditioned fear-evoking stimulus. Exposure to TMT induces robust c-Fos activity in the BNST (Day et al, 2004; Asok et al, 2013), and inactivation of the BNST blocks TMT-evoked freezing (Fendt et al, 2003)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call