Histological verification of optogenetic targeting of noradrenergic LC neurons.

(A) To verify viral expression, the locus coeruleus (LC) was stained with tyrosine hydroxylase (TH) primary antibody along with secondary antibody with AlexaFluor 488 to identify TH-positive neurons in the region of the LC. The same tissue was counterstained with mCherry primary antibody and enhanced with AlexaFluor 568 to determine the overlap of virally infected TH-positive cells. 69 ± 5% of noradrenergic LC cells were infected with AAV5-EF1a-DIO-ChR2(H134R)-mCherry, with an example provided in the overlay. (B) The approximate probe tip locations in each animal are displayed confirming successful targeting of the LC, with shades of blue representing animals expressing ChR2 (C), and shades of red representing control animals infected with AAV5-EF1a-DIO-mCherry (D). When the behaviour of multiple control groups was compared, TH-Cre and LE rats expressing control virus and receiving light delivery during stimulus presentation in extinction, as well as Offset controls expressing ChR2 virus and receiving light delivery during the ITI of extinction sessions showed no significant differences in response rates on the final day of training (E), during extinction sessions with light delivery (F), or during tests of spontaneous recovery conducted without stimulation the next day (Test 1) and again one week later (Test 2; (G; p>0.05). These multiple control groups are therefore collapsed in subsequent analyses.

Optogenetic stimulation of the LC enhances long-term expression of extinction.

(A) Schematic representation of the study design. All groups received identical discriminated operant training where lever-pressing during 20-s presentations of a discriminative stimulus was reinforced with a food pellet. Responding in the absence of the discriminative stimuli was not reinforced. The groups differed in the period of time in which optical manipulation of the LC took place during extinction sessions with the timing of light delivery indicated by the blue bars; for Control and ChR2 groups light was delivered during stimulus presentations (gray bars) when reward was expected based on previous training, but not delivered; the Offset group received similar LC stimulation but offset from stimulus presentations (i.e., during the ITI). The 3 groups (Control, ChR2, and Offset groups), showed similar response rates in training (B; p>0.05). Responding in all groups extinguished when reward was omitted (p<0.05) and no differences were observed between groups (C; p>0.05). When tested the next day for spontaneous recovery, the ChR2 group displayed significantly fewer lever presses than the Control or Offset groups, suggesting LC stimulation strengthened extinction learning (D, Test 1; p<0.05). A similar effect was observed one week later indicating a persistent effect of LC stimulation on later retention of extinction (D, Test 2; p<0.05).

Optogenetic stimulation of the LC does not produce conditioned aversion.

A conditioned place preference/aversion test was performed to determine if LC stimulation produced aversive conditioning. Rats expressing ChR2 were placed in an apparatus with two chambers separated by a sliding door, depicted in (A). One chamber, labelled Context A, had a yellow background with vertical stripes. A second chamber, labelled Context B had a green background with blue circles. All rats were given 3 days to freely explore both chambers for 10 min per day. Afterwards, the door was closed, and rats were confined to one context (A or B, counterbalanced) where they received eight 20 s bouts of LC stimulation at 10 Hz (160 s total stimulation time) within the 10-min session. On alternating days rats were confined to the other context (B or A, counterbalanced) without stimulation. On the test day, the sliding door opened and rats were given 10 min to freely explore. The total time spent in each context was recorded. A rat was considered to be in one chamber when both hindfeet were inside the chamber. No preference for either context was observed as rats spent a near-equal amount of time in both chambers (B), suggesting no aversive associations with the context formed as a result of optogenetic stimulation of the LC with the parameters used here.

Optogenetic inhibition of the LC did not impair the long-term expression of extinction.

LC neurons were successfully targeted with halorhodopsin-expressing virus (AAV5-EF1a-DIO-eNpHR3.0-mCherry) or a control virus (AAV5-EF1a-DIO-mCherry) as shown in (A). Green represents TH-positive neurons, red represents virally infected neurons expressing mCherry, and infected TH-positive cells are shown in the overlay (55±8.7% infection rate). The locations of probe tips are shown with shades of green representing animals expressing eNpHR (B), and shades of red representing control animals (C). (D) Schematic representation of training and testing. Gray bars represent stimulus presentations and yellow bars represent light delivery. Both groups underwent identical discriminated operant training and showed comparable response rates at the end of acquisition (E; p>0.05). Control and eNpHR groups were then given LC light delivery during stimulus trials over three extinction sessions. Photoinhibition of the LC during extinction training reduced mean response rates compared to control rats (F; F(1,13)=6.899, p=0.021) but this difference did not persist to tests conducted one (Test 1) and seven (Test 2) days later where no group differences were observed in spontaneous recovery (G; p>0.05).