The cation channel mechanisms of subthreshold inward depolarizing currents in the VTA dopaminergic neurons and their roles in the depression-like behavior

Reviewer #1 (Public Review):

Wang et al., present a paper aiming to identify NALCN and TRPC6 channels as key mechanisms regulating VTA dopaminergic neuron spontaneous firing and investigating whether these mechanisms are disrupted in a chronic unpredictable stress model mouse.

Major strengths:

-This paper uses multiple approaches to investigate the role of NALCN and TRPC6 channels in VTA dopaminergic neurons.

Major weaknesses:

-The pharmacological tools used in this study are highly non-selective. Gd3+, used here to block NALCN is actually more commonly used to block TRP channels. 2-APB inhibits not only TRPC channels, but also TRPM and IP3 receptors while stimulating TRPV channels (Bon and Beech, 2013), while FFA actually stimulates TRPC6 channels while inhibiting other TRPCs (Foster et al., 2009).

Are the author's claims supported by the data?

-The multimodal approach including shRNA knockdown experiments alleviates much of the concern about the non-specific pharmacological agents. Therefore, the author's claim that NALCN is involved in VTA dopaminergic neuron pacemaking is well-supported.

-However, the claim that TRPC6 is the key TRPC channel in VTA spontaneous firing is somewhat, but not completely supported. As with NALCN above, the pharmacology alone is much too non-specific to support the claim that TRPC6 is the TRP channel responsible for pacemaking. However, unlike the NALCN condition, there is an issue with interpreting the shRNA knockdown experiments. The issue is that TRPC channels often form heteromers with TRPC channels of other types (Goel, Sinkins and Schilling, 2002; Strübing et al., 2003). Therefore, it is possible that knocking down TRPC6 is interfering with the normal function of another TRPC channel, such as TRPC7 or TRPC4.

-The claim that TRPC6 channels in the VTA are involved in the depressive-like symptoms of CMUS is supported.

- However, the connection between the mPFC-projecting VTA neurons, TRPC6 channels, and the chronic unpredictable stress model (CMUS) of depression is not well supported. In Figure 2, it appears that the mPFC-projecting VTA neurons have very low TRPC6 expression compared to VTA neurons projecting to other targets. However, in figure 6, the authors focus on the mPFC-projecting neurons in their CMUS model and show that it is these neurons that are no longer sensitive to pharmacological agents non-specifically blocking TRPC channels (2-APB, see above comment). Finally, in figure 7, the authors show that shRNA knockdown of TRPC6 channels (in all VTA dopaminergic neurons) results in depressive-like symptoms in CMUS mice. Due to the low expression of TRPC6 in mPFC-projecting VTA neurons, the author's claims of "broad and strong expression of TRPC6 channels across VTA DA neurons" is not fully supported. Because of the messy pharmacological tools used, it cannot be clamed that TRPC6 in the mPFC-projecting VTA neurons is altered after CMUS. And because the knockdown experiments are not specific to mPFC-projecting VTA neurons, it cannot be claimed that reducing TRPC6 in these specific neurons is causing depressive symptoms.

Impact:

It is valuable to compare pacemaking mechanisms in VTA and SNc neurons and this paper convincingly shows that NALCN contributes to VTA pacemaking, as it is known to contribute to SNc pacemaking. It also shows that TRPC6 channels in VTA dopamine neurons contribute to the depressive-like symptoms associated with CMUS.

It is important to note that the experiments presented in Figure 1 have all been previously performed in VTA dopaminergic neurons (Khaliq and Bean, 2010) including showing that low calcium increases VTA neuron spontaneous firing frequency and that replacement of sodium with NMDG hyperpolarizes the membrane potential.

Additional context:

-The authors explanation for the increase in firing frequency in 0 calcium conditions is that calcium-activated potassium channels would no longer be activated. However, there is a highly relevant finding that low calcium enhances the NALCN conductance through the calcium sensing receptor from Dejian Ren's lab (Lu et al., 2010) which is not cited in this paper. This increase in NALCN conductance with low calcium has been shown in SNc dopaminergic neurons (Philippart and Khaliq, 2018), and is likely a factor contributing to the low-calcium-mediated increase in spontaneous VTA neuron firing.

-One of the only demonstrations of the expression and physiological significance of TRPCs in VTA DA neurons was published by (Rasmus et al., 2011; Klipec et al., 2016) which are not cited in this paper. In their study, TRPC4 expression was detected in a uniformly distributed subset of VTA DA neurons, and TRPC4 KO rats showed decreased VTA DA neuron tonic firing and deficits in cocaine reward and social behaviors.

- Out of all seven TRPCs, TRPC5 is the only one reported to have basal/constitutive activity in heterologous expression systems (Schaefer et al., 2000; Jeon et al., 2012). Others TRPCs such as TRPC6 are typically activated by Gq-coupled GPCRs. Why would TRPC6 be spontaneously/constitutively active in VTA DA neurons?

-A new paper from the group of Myoung Kyu Park (Hahn et al., 2023) shows in great detail the interactions between NALCN and TRPC3 channels in pacemaking of SNc DA neurons.

References

Bon, R.S. and Beech, D.J. (2013) 'In pursuit of small molecule chemistry for calcium-permeable non-selective TRPC channels -- mirage or pot of gold?', British Journal of Pharmacology, 170(3), pp. 459-474. Available at: https://doi.org/10.1111/bph.12274.

Foster, R.R. et al. (2009) 'Flufenamic acid is a tool for investigating TRPC6-mediated calcium signalling in human conditionally immortalised podocytes and HEK293 cells', Cell Calcium, 45(4), pp. 384-390. Available at: https://doi.org/10.1016/j.ceca.2009.01.003.

Goel, M., Sinkins, W.G. and Schilling, W.P. (2002) 'Selective association of TRPC channel subunits in rat brain synaptosomes', The Journal of Biological Chemistry, 277(50), pp. 48303-48310. Available at: https://doi.org/10.1074/jbc.M207882200.

Hahn, S. et al. (2023) 'Proximal dendritic localization of NALCN channels underlies tonic and burst firing in nigral dopaminergic neurons', The Journal of Physiology, 601(1), pp. 171-193. Available at: https://doi.org/10.1113/JP283716.

Jeon, J.-P. et al. (2012) 'Selective Gαi subunits as novel direct activators of transient receptor potential canonical (TRPC)4 and TRPC5 channels', The Journal of Biological Chemistry, 287(21), pp. 17029-17039. Available at: https://doi.org/10.1074/jbc.M111.326553.

Khaliq, Z.M. and Bean, B.P. (2010) 'Pacemaking in dopaminergic ventral tegmental area neurons: depolarizing drive from background and voltage-dependent sodium conductances', The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, 30(21), pp. 7401-7413. Available at: https://doi.org/10.1523/JNEUROSCI.0143-10.2010.

Klipec, W.D. et al. (2016) 'Loss of the trpc4 gene is associated with a reduction in cocaine self-administration and reduced spontaneous ventral tegmental area dopamine neuronal activity, without deficits in learning for natural rewards', Behavioural Brain Research, 306, pp. 117-127. Available at: https://doi.org/10.1016/j.bbr.2016.03.027.

Lu, B. et al. (2010) 'Extracellular calcium controls background current and neuronal excitability via an UNC79-UNC80-NALCN cation channel complex', Neuron, 68(3), pp. 488-499. Available at: https://doi.org/10.1016/j.neuron.2010.09.014.

Philippart, F. and Khaliq, Z.M. (2018) 'Gi/o protein-coupled receptors in dopamine neurons inhibit the sodium leak channel NALCN', eLife, 7. Available at: https://doi.org/10.7554/eLife.40984.

Rasmus, K. et al. (2011) 'Sociability is decreased following deletion of the trpc4 gene', Nature Precedings, pp. 1-1. Available at: https://doi.org/10.1038/npre.2011.6367.1.

Schaefer, M. et al. (2000) 'Receptor-mediated regulation of the nonselective cation channels TRPC4 and TRPC5', The Journal of Biological Chemistry, 275(23), pp. 17517-17526. Available at: https://doi.org/10.1074/jbc.275.23.17517.

Strübing, C. et al. (2003) 'Formation of novel TRPC channels by complex subunit interactions in embryonic brain', The Journal of Biological Chemistry, 278(40), pp. 39014-39019. Available at: https://doi.org/10.1074/jbc.M306705200.

Reviewer #2 (Public Review):

This paper describes the results of a set of complementary and convergent experiments aimed at describing roles for the non-selective cation channels NALCN and TRPC6 in mediating subthreshold inward depolarizing currents and action potential generation in VTA DA neurons under normal physiological conditions. That said, some datasets are underpowered, and general flaws in statistical reporting make assessment difficult. There is also a lack of clarity at various points throughout the manuscript, as well as overinterpretation of the data generated in these experiments. Specific comments follow:

1. These results do not show that TRPC6 mediates stress effects on depression-like behavior. As stated by the authors in the first sentence of the final paragraph, "downregulation of TRPC6 proteins was correlated with reduced firing activity of the VTA DA neurons, the depression-like behaviors, and that knocking down of TRPC6 in the VTA DA neurons confer the mice with depression behaviors." Therefore, the results show associations between TRPC6 downregulation and stress effects on behavior, occlusion of the effects of one by the other on some outcome measures, and cell manipulation effects that resemble stress effects. There is no experiment that shows reversal of stress effects with cell/circuit-specific TRPC6 manipulations. Please adjust the title, abstract and interpretation accordingly.
2. Statistical tests and results are unclear throughout. For all analyses, please report specific tests used, factors/groups, test statistic and p-value for all data analyses reported. In some cases, the chosen test is not appropriate. For example, in Figure 6E, it is not clear how an experiment with 2 factors (stress and drug) can be analyzed with a 1-way RM ANOVA. The potential impact of inappropriate statistical tests on results makes it difficult to assess the accuracy of data interpretation.
3. Why were only male mice used? Please justify and discuss in the manuscript. Also, change the title to reflect this.
4. Number of recorded cells is very low in Figure 1. Where in VTA did recordings occur? Given the heterogeneity in this brain region, this n may be insufficient. Additional information (e.g., location within VTA, criteria used to identify neurons) should be included. Report the number of mice (i.e., n = 6 cells from X mice) in all figures.
5. Authors refer to VTA DA neurons as those that are DAT+ in line 276, although TH expression is considered the standard of DAergic identity, and studies (e.g., Lammel et al, 2008) have shown that a subset of VTA DA neurons have low levels of DAT expression. Authors should reword/clarify that these are DAT-expressing VTA DA neurons.
6. Neuronal subtype proportions should be quantified and reported (Fig. 1Aii).
7. In addition to reporting projection specificity of neurons expressing specific channels, it would be ideal to report these data according to spatial location in VTA.
8. The authors state that there are a small number of Glut neurons in VTA, then they state that a "significant proportion" of VTA neurons are glutamatergic.
9. It is an overstatement that VTA DA neurons are the key determinant of abnormal behaviors in affective disorders.

Reviewer #3 (Public Review):

The authors of this study have examined which cation channels specifically confer to ventral tegmental area dopaminergic neurons their autonomic (spontaneous) firing properties. Having brought evidence for the key role played by NALCN and TRPC6 channels therein, the authors aimed at measuring whether these channels play some role in so-called depression-like (but see below) behaviors triggered by chronic exposure to different stressors. Following evidence for a down-regulation of TRPC6 protein expression in ventral tegmental area dopaminergic cells of stressed animals, the authors provide evidence through viral expression protocols for a causal link between such a down-regulation and so-called depression-like behaviors. The main strength of this study lies on a comprehensive bottom-up approach ranging from patch-clamp recordings to behavioral tasks. However, the interpretation of the results gathered from these behavioral tasks might also be considered one main weakness of the abovementioned approach. Thus, the authors make a confusion (widely observed in numerous publications) with regard to the use of paradigms (forced swim test, tail suspension test) initially aimed (and hence validated) at detecting the antidepressant effects of drugs and which by no means provide clues on "depression" in their subjects. Indeed, in their hands, the authors report that stress elicits changes in these tests which are opposed to those theoretically seen after antidepressant medication. However, these results do not imply that these changes reflect "depression" but rather that the individuals under scrutiny simply show different responses from those seen in nonstressed animals. These limits are even more valid in nonstressed animals injected with TRPC6 shRNAs (how can 5-min tests be compared to a complex and chronic pathological state such as depression?). With regard to anxiety, as investigated with the elevated plus-maze and the open field, the data, as reported, do not allow to check the author's interpretation as anxiety indices are either not correctly provided (e.g. absolute open arm data instead of percents of open arm visits without mention of closed arm behaviors) or subjected to possible biases (lack of distinction between central and peripheral components of the apparatus).

Author Response

Reviewer #1 (Public Review):

Comment 1:

The pharmacological tools used in this study are highly non-selective. Gd3+, used here to block NALCN is actually more commonly used to block TRP channels. 2-APB inhibits not only TRPC channels, but also TRPM and IP3 receptors while stimulating TRPV channels (Bon and Beech, 2013), while FFA actually stimulates TRPC6 channels while inhibiting other TRPCs (Foster et al., 2009).

We agree with the reviewer that the substances mentioned are not specific. Although we performed shRNA experiments against NALCN and TRPC6, we do plan to use more specific pharmacological modulators for these two channels; for this, L703,606 (the antagonist of NALCN) [1] and larixyl acetate (a potent TRPC6 inhibitor) [2] will be used. Actually, we have completed experiments of using larixyl acetate and the results are shown in Author response image 1.

Author response image 1.

Example time-course (A), traces (B) and the summaried data (C) for the effect of larixyl acetate (LA), the antagonist of TRPC6 channel, on the spontaneous firing activity of VTA DA neurons. Paired-sample T test, ** P < 0.01. n is number of neurons recorded and N is number of mice used

Comment 2:

The multimodal approach including shRNA knockdown experiments alleviates much of the concern about the non-specific pharmacological agents. Therefore, the author's claim that NALCN is involved in VTA dopaminergic neuron pacemaking is well-supported.

However, the claim that TRPC6 is the key TRPC channel in VTA spontaneous firing is somewhat, but not completely supported. As with NALCN above, the pharmacology alone is much too non-specific to support the claim that TRPC6 is the TRP channel responsible for pacemaking. However, unlike the NALCN condition, there is an issue with interpreting the shRNA knockdown experiments. The issue is that TRPC channels often form heteromers with TRPC channels of other types (Goel, Sinkins and Schilling, 2002; Strübing et al., 2003). Therefore, it is possible that knocking down TRPC6 is interfering with the normal function of another TRPC channel, such as TRPC7 or TRPC4.

According with your advice, we plan to perform single-cell qPCR experiments to check the expression level of other TRPC channels, after selective knockdown of TRPC6 in VTA DAT+ neurons, results will be shown later in the revised version. From our single-cell RNA-seq results, TRPC7 and TRPC4 are found not to be present broadly like TRPC6 in the VTA DA neurons, therefore it is possible that knocking down TRPC6 maybe not interfering with the normal function of another TRPC channel, such as TRPC7 or TRPC4.

Comment 3:

The claim that TRPC6 channels in the VTA are involved in the depressive-like symptoms of CMUS is supported.

However, the connection between the mPFC-projecting VTA neurons, TRPC6 channels, and the chronic unpredictable stress model (CMUS) of depression is not well supported. In Figure 2, it appears that the mPFC-projecting VTA neurons have very low TRPC6 expression compared to VTA neurons projecting to other targets. However, in figure 6, the authors focus on the mPFC-projecting neurons in their CMUS model and show that it is these neurons that are no longer sensitive to pharmacological agents non-specifically blocking TRPC channels (2-APB, see above comment). Finally, in figure 7, the authors show that shRNA knockdown of TRPC6 channels (in all VTA dopaminergic neurons) results in depressive-like symptoms in CMUS mice. Due to the low expression of TRPC6 in mPFC-projecting VTA neurons, the author's claims of "broad and strong expression of TRPC6 channels across VTA DA neurons" is not fully supported. Because of the messy pharmacological tools used, it cannot be clamed that TRPC6 in the mPFC-projecting VTA neurons is altered after CMUS. And because the knockdown experiments are not specific to mPFC-projecting VTA neurons, it cannot be claimed that reducing TRPC6 in these specific neurons is causing depressive symptoms.

The reason we focused on the mPFC-projecting VTA DA neurons is that this pathway is indicated in depressive-like behaviors of the CMUS model[3-5]. Although mPFC-projecting VTA DA neurons seem have lower level of TRPC6, we reason they are still functional there. However, we do agree with the reviewer that the statement “broad and strong expression of TRPC6 channels across VTA DA neurons" is not fully supported. We have changed the statements based on the reviewer suggestion. Furthermore, we also plan to selectively knockdown TRPC6 in the mPFC-projecting VTA DA neurons, and then study the behavior.

Comment 4:

It is important to note that the experiments presented in Figure 1 have all been previously performed in VTA dopaminergic neurons (Khaliq and Bean, 2010) including showing that low calcium increases VTA neuron spontaneous firing frequency and that replacement of sodium with NMDG hyperpolarizes the membrane potential.

We agree with reviewer that similar experiments have been performed previously [6]for the flow of our manuscript and for general readers.

Comment 5:

The authors explanation for the increase in firing frequency in 0 calcium conditions is that calcium-activated potassium channels would no longer be activated. However, there is a highly relevant finding that low calcium enhances the NALCN conductance through the calcium sensing receptor from Dejian Ren's lab (Lu et al., 2010) which is not cited in this paper. This increase in NALCN conductance with low calcium has been shown in SNc dopaminergic neurons (Philippart and Khaliq, 2018), and is likely a factor contributing to the low-calcium-mediated increase in spontaneous VTA neuron firing.

We agree with the reviewer and thanks for the suggestions. A discussion for this has been added.

Comment 6:

One of the only demonstrations of the expression and physiological significance of TRPCs in VTA DA neurons was published by (Rasmus et al., 2011; Klipec et al., 2016) which are not cited in this paper. In their study, TRPC4 expression was detected in a uniformly distributed subset of VTA DA neurons, and TRPC4 KO rats showed decreased VTA DA neuron tonic firing and deficits in cocaine reward and social behaviors.

We thank the reviewer for the suggestion.The references and a discussion for this has been added.

Comment 7:

Out of all seven TRPCs, TRPC5 is the only one reported to have basal/constitutive activity in heterologous expression systems (Schaefer et al., 2000; Jeon et al., 2012). Others TRPCs such as TRPC6 are typically activated by Gq-coupled GPCRs. Why would TRPC6 be spontaneously/constitutively active in VTA DA neurons?

In a complex neuronal environment where VTA DA neurons are located, multiple modulatory factors including the GPCRs could be dynamically active, this could lead to the activation of TRP channels including TRPC6.

Comment 8:

A new paper from the group of Myoung Kyu Park (Hahn et al., 2023) shows in great detail the interactions between NALCN and TRPC3 channels in pacemaking of SNc DA neurons.

The reference mentioned has been added. We thank the reviewer.

Reviewer #2 (Public Review):

Comment 1:

These results do not show that TRPC6 mediates stress effects on depression-like behavior. As stated by the authors in the first sentence of the final paragraph, "downregulation of TRPC6 proteins was correlated with reduced firing activity of the VTA DA neurons, the depression-like behaviors, and that knocking down of TRPC6 in the VTA DA neurons confer the mice with depression behaviors." Therefore, the results show associations between TRPC6 downregulation and stress effects on behavior, occlusion of the effects of one by the other on some outcome measures, and cell manipulation effects that resemble stress effects. There is no experiment that shows reversal of stress effects with cell/circuit-specific TRPC6 manipulations. Please adjust the title, abstract and interpretation accordingly.

We agree with the reviewer’s suggestion. The title was changed to ‘’The cation channel mechanisms of subthreshold inward depolarizing currents in the VTA dopaminergic neurons and their roles in the chronic stress-induced depression-like behavior” and the abstract and interpretation were also adjusted accordingly.

Comment 2:

Statistical tests and results are unclear throughout. For all analyses, please report specific tests used, factors/groups, test statistic and p-value for all data analyses reported. In some cases, the chosen test is not appropriate. For example, in Figure 6E, it is not clear how an experiment with 2 factors (stress and drug) can be analyzed with a 1-way RM ANOVA. The potential impact of inappropriate statistical tests on results makes it difficult to assess the accuracy of data interpretation.

We have redone the statistical analysis as suggested by the reviewer and added specific tests used, factors/groups, test statistic and p-value for all data analyses into the revised manuscript.

Comment 3:

Why were only male mice used? Please justify and discuss in the manuscript. Also, change the title to reflect this.

Although most similar previous studies used male mice or rats[7, 8], we do agree with the reviewer that the female animals should also be tested, in consideration possible role of sex hormones, as such we plan to repeat some key experiments on female mice.

Comment 4:

Number of recorded cells is very low in Figure 1. Where in VTA did recordings occur? Given the heterogeneity in this brain region, this n may be insufficient. Additional information (e.g., location within VTA, criteria used to identify neurons) should be included. Report the number of mice (i.e., n = 6 cells from X mice) in all figures.

Yes indeed, the number here is not high. More experiments will be performed to increase the N/n number. And the location of recorded cells in VTA and the number of used mice are now shown in all figures; criteria to identify neurons is stated in the Methods- Identification of DA neurons and electrophysiological recordings. At the end of electrophysiological recordings, the recorded VTA neurons were collected for single-cell PCR. VTA DA neurons were identified by single-cell PCR for the presence of TH and DAT.

Comment 5:

Authors refer to VTA DA neurons as those that are DAT+ in line 276, although TH expression is considered the standard of DAergic identity, and studies (e.g., Lammel et al, 2008) have shown that a subset of VTA DA neurons have low levels of DAT expression. Authors should reword/clarify that these are DAT-expressing VTA DA neurons.

The study published by Lammel[9] in 2015 has shown the low dopamine specificity of transgene expression in ventral midbrain of TH-Cre mice; on the other hand, DAT-Cre mice exhibit dopamine-specific Cre expression patterns, although DAT-Cre mice are likely to suffer from their own limitations (for example, low DAT expression in mesocortical DA neurons may make it difficult to target this subpopulation, see Lammel et al., 2008[10]). Hence, in our study, the DAT was used as criteria to identify DAT neurons. Of course, TH and DAT were all tested in single-cell PCR to identify whether the recorded cells were DA neurons.

Comment 6:

Neuronal subtype proportions should be quantified and reported (Fig. 1Aii).

Neuronal subtype proportions are now quantified and reported in Fig. 1Aii.

Comment 7:

In addition to reporting projection specificity of neurons expressing specific channels, it would be ideal to report these data according to spatial location in VTA.

The spatial location of recorded cells in VTA are now shown in all figures.

Comment 8:

The authors state that there are a small number of Glut neurons in VTA, then they state that a "significant proportion" of VTA neurons are glutamatergic.

Thanks, “a significant proportion of neurons” has been changed to “ less than half of sequenced DA neurons”.

Comment 9:

It is an overstatement that VTA DA neurons are the key determinant of abnormal behaviors in affective disorders.

Thanks, we have amended the statement to that “Dopaminergic (DA) neurons in the ventral tegmental area (VTA) play an important role in mood, reward and emotion-related behaviors”.

Reviewer #3 (Public Review):

Comment 1:

The authors of this study have examined which cation channels specifically confer to ventral tegmental area dopaminergic neurons their autonomic (spontaneous) firing properties. Having brought evidence for the key role played by NALCN and TRPC6 channels therein, the authors aimed at measuring whether these channels play some role in so-called depression-like (but see below) behaviors triggered by chronic exposure to different stressors. Following evidence for a down-regulation of TRPC6 protein expression in ventral tegmental area dopaminergic cells of stressed animals, the authors provide evidence through viral expression protocols for a causal link between such a down-regulation and so-called depression-like behaviors. The main strength of this study lies on a comprehensive bottom-up approach ranging from patch-clamp recordings to behavioral tasks. However, the interpretation of the results gathered from these behavioral tasks might also be considered one main weakness of the abovementioned approach. Thus, the authors make a confusion (widely observed in numerous publications) with regard to the use of paradigms (forced swim test, tail suspension test) initially aimed (and hence validated) at detecting the antidepressant effects of drugs and which by no means provide clues on "depression" in their subjects. Indeed, in their hands, the authors report that stress elicits changes in these tests which are opposed to those theoretically seen after antidepressant medication. However, these results do not imply that these changes reflect "depression" but rather that the individuals under scrutiny simply show different responses from those seen in nonstressed animals. These limits are even more valid in nonstressed animals injected with TRPC6 shRNAs (how can 5-min tests be compared to a complex and chronic pathological state such as depression?). With regard to anxiety, as investigated with the elevated plus-maze and the open field, the data, as reported, do not allow to check the author's interpretation as anxiety indices are either not correctly provided (e.g. absolute open arm data instead of percents of open arm visits without mention of closed arm behaviors) or subjected to possible biases (lack of distinction between central and peripheral components of the apparatus).

We agree with the reviewer that behavior tests we used here is debatable whether they represent a real depression state, and this is an open question that could be discussed from different respective. Since these testes (forced swimming and tail suspension), as the reviewer noted, were “widely observed in numerous publications”, we used these seemly only options to reflect a “depression-like” state. One could argue that since these testes were initially used for testing antidepressants (“validated”), with decreased immobility time as indications of anti-depressive effects, why not an increased immobility time reflect a “depression-like” state. As for anxiety tests, both absolute time in open and closed arms are now provided.