Major depressive disorder is the main cause of disability worldwide with imperfect treatment options. However, novel therapeutic approaches are currently discussed, from augmentation strategies to novel treatments targeting the immune system or the microbiome-gut-brain axis. Therefore, we examined the potential beneficial effects of minocycline, a tetracycline antibiotic with pleiotropic, immunomodulatory action, alone or as augmentation of escitalopram on behavior, prefrontal microglial density, and the gut microbiome in rats selectively bred for high anxiety-like behavior (HAB). We show that concomitant with their high innate anxiety and depression, HABs have lower microglial numbers in the infralimbic and prelimbic prefrontal cortex and an altered gut microbiota composition compared with controls. Three weeks of minocycline treatment alleviated the depressive-like phenotype, further reduced microglial density, exclusively in male HAB rats, and reduced plasma concentrations of pro-inflammatory cytokines. However, coadministration of escitalopram, which had no effect alone, prevented these minocycline-induced effects. Moreover, minocycline led to a robust shift in cecal microbial composition in both HABs and rats non-selected for anxiety-like behavior. Minocycline markedly increased relative abundance of Lachnospiraceae and Clostridiales Family XIII, families known for their butyrate production, with a corresponding increase and positive correlation in plasma 3-OH-butyrate levels in a trait-dependent manner. Thus, our data suggest that the antidepressant effect of minocycline is sex- and trait-dependent, associated with a reduced microglial number in the prefrontal cortex, and with changes in microbial composition and their metabolites. These results further support the microbiome-gut–brain axis as potential target in the treatment of depression.
According to the World Health Organization, depression has become the leading cause of disability worldwide affecting approximately 300 million people with a lifetime prevalence of 10.7% in men and 18.1% in women in the US1. Numerous treatment options for major depressive disorder (MDD) are available such as the frequently prescribed and highly efficacious selective serotonin reuptake inhibitor (SSRI) escitalopram2,3. However, antidepressants display a therapeutic lag of 2–4 weeks, and only 70% of patients respond sufficiently4. To achieve therapies with faster onset, two major approaches can be utilized, i.e. optimization of existing options or the discovery of agents with novel mechanisms of action. Treatment regimens move towards augmentation strategies, a combination of conventional antidepressants with non-antidepressant substances to increase efficacy and overcome treatment resistance5. Regarding novel targets, central inflammation and the microbiome-gut–brain axis are two areas receiving growing traction6,7.
Thus, dysregulation in microglia, the immune system of the brain, as well as the gut microbiome have been associated with MDD8,9,10,11. A significant influence of microbiota on microglia activation and maturation, potentially via bacteria-produced short-chain fatty acids like butyrate, has been reported12,13. This points towards a complex role of microbiota and microglia in anxiety and depression, suggesting a subtle interplay between behavior, microglia and microbiota. In light of this, one attractive treatment option is the pleiotropic broad-spectrum tetracycline antibiotic minocycline, with neuroprotective and anti-inflammatory properties, e.g. inhibiting microglial activation14,15,16,17, which also affects gut microbiota18. Recent clinical studies have shown that minocycline can augment the clinical efficacy of antidepressants19,20,21, an effect that was proposed to be dependent on the presence of an inflammatory state22. These findings are supported by several rodent studies showing that minocycline promotes active stress coping23,24 and reverses inflammation-induced25,26 as well as stress-induced depressive-like behavior27,28. However, substantial evidence is required from appropriate animal models regarding behavioral effects of minocycline and particularly relating to its mechanism(s) of action.
One of the most heuristic approaches to develop appropriate animal models is via selective breeding for a particular trait29. This approach gave rise to Wistar rats with extremely high anxiety-related behavior (HAB) based on their performance on the elevated plus-maze (EPM), a phenotype repeatedly confirmed independent of sex. Moreover, HAB rats consistently show similar characteristics as observed in MDD patients including passive stress-coping, altered serotonin and neuropeptide signaling in the brain and, consequently, dysregulated responses of the hypothalamic–pituitary–adrenal (HPA) axis30,31,32,33. The highly anxious and depressive-like phenotype of male HAB rats has been successfully reversed by chronic citalopram or paroxetine treatment34,35. However, this required an 8-week treatment regimen, suggesting HAB rats as an animal model for comorbid anxiety and depression, as well as treatment-resistant depression. Amelioration of these behavioral deficits in female HAB rats remains to be studied, an approach urgently needed considering the more frequent diagnosis of MDD in women30.
Changes in several cortical and limbic structures like the hippocampus, amygdala and especially the prefrontal cortex (PFC) are documented in the pathophysiology of depression36,37,38,39,40. Fittingly, intra-PFC citalopram microinfusion acted as an antidepressant41, whereas glial loss in this region facilitated depressive-like behavior42. Moreover, stress- or inflammation-induced depressive-like behavior paralleled by PFC microglial activation was prevented by minocycline treatment25,27,43. Importantly, acute inactivation of the infralimbic cortex in HAB rats attenuated depressive-like behavior, corresponding to the behavioral consequences of deep brain stimulation of Brodmann Area 25 in MDD patients39,44, indicating the translational relevance of this animal model and the importance of this region.
Based on these prerequisites, we assessed the effects of chronic minocycline treatment on anxiety- and depressive-like behavior in rats in dependence on trait anxiety levels in both sexes. For translational comparison with clinical studies using minocycline as an add-on treatment, the standard SSRI escitalopram and the augmentation of minocycline with escitalopram were included. In order to approach potential mechanisms underlying the differential treatment effects, we further examined microglia density in the PFC, peripheral immune function comprising pro-inflammatory cytokines, and alterations in gut microbiota. Male and female rats non-selected for anxiety (NAB) were included to determine a trait-dependency of treatment.
Methods and materials
Male and female NAB rats were either purchased from Charles River (Wistar rats; Sulzfeld, Germany) or, like all male and female HAB rats, bred at the University of Regensburg. HAB rats showing <10% of time spent on the open arms of an EPM at the age of 9 weeks were selected45. All rats were maintained on a 12-h light–dark cycle in a temperature controlled colony (22–24 °C; 55±5% Humidity) with free access to food and tap water (vehicle) or drug solution (minocycline and/or escitalopram, see experimental design) under facility-specific husbandry conditions according to the respective EU regulations (2010/63/EU). All experimental procedures were approved by the Committee on Animal Health and Care of the local government, and performed according to the Guide for the Care and Use of Laboratory Animals of the Government of Oberpfalz and Unterfranken, the ARRIVE guidelines46, and recommendations from the NIH.
At the age of 11–12 weeks, rats were group-housed in cages of 3–4 rats according to their experimental group (i.e. sex and trait) and randomly assigned to the treatment. Body weight and water consumption were monitored daily to calculate the respective concentrations needed for oral drug administration via drinking water and to prepare fresh solutions daily. In the first set of experiments, 40 mg/kg/day minocycline43, 10 mg/kg/day escitalopram47, or a combination of both substances with the same concentrations, while in the second set, 80 mg/kg/day minocycline alone, all dissolved in tap water, was applied for 22 days. The treatment duration was chosen based on the fact that antidepressant treatment generally needs 2–3 weeks for the onset of therapeutic efficacy48 and on a previous study showing an antidepressant effect of minocycline already after 7 days28. Minocycline hydrochloride and escitalopram oxalate were kindly provided by the Charité Berlin and Lundbeck A/S (Copenhagen, Denmark), respectively.
Rats were tested in the social preference test (SPT; day 15), in the light–dark box (LDB; day 17) and on the EPM (day 19), as well as in the forced swim test (FST; day 22; Fig. 1a). Behavioral tests were conducted between 0900 and 1200 except for the SPT (1900 to 2200) and behavioral analysis was conducted by an observer blind to the trait and treatment. Vaginal smears were taken after the EPM and FST to control for estrous cycle. Immediately after the FST, all rats were deeply anesthetized for transcardial perfusion (1x phosphate buffered saline and 4% paraformaldehyde), and blood, liver, fecal boli, and cecal samples were collected, snap frozen using dry ice and stored at −80 °C until further analyses. Microglia quantity was analyzed by immunofluorescent-immunohistochemistry of the microglial marker ionized calcium-binding adapter molecule-1 (Iba-1, Wako, 019-19741) on 40 µm coronal brain sections from the infralimbic and prelimbic PFC. For method details see Supplementary Methods.
Minocycline tissue extraction and HPLC analyses
A sensitive and specific reversed-phase high-performance liquid chromatographic (HPLC) method was developed and optimized for detection of minocycline in liver tissue and fecal boli. The limit of quantitation was 50 ng/ml with an averaged recovery from homogenates of 95%, with a 5–10% intra- and inter-assay coefficient (see Supplementary Methods).
Determination of plasma beta-hydroxybutyrate levels
Beta-hydroxybutyrate concentrations (3-OH-butyrate; stimulated by butyrate release) in plasma were determined with a commercial assay kit (Sigma-Aldrich, Germany). The enzyme reaction results in a colorimetric product proportional to the presence of the metabolite 3-OH-butyrate (see Supplementary Methods).
Luminex® cytokine detection assay
Interferon (IFN)-γ and interleukin (IL)-12p40 concentrations were quantified in plasma using a cytokine bead immunoassay (Invitrogen/ThermoFisher Scientific, Darmstadt, Germany) and the Luminex xMAP 100 system (Luminex, Austin, TX, USA) according to the manufacturer’s protocol (see Supplementary Methods).
Intestinal microbiome analysis by 16S-rDNA pyrosequencing
The methods used for the isolation of DNA from stool specimens, quantification of 16S-rDNA copies by qPCR, PCR amplification of V3-V6 16S-rDNA variable regions, 454 pyrosequencing (see Supplementary Table S1 for primer sequences), sequence processing and operational taxonomic unit (OTU) clustering as well as analysis of microbial composition and global community structure are described in the Supplementary Methods.
Behavioral data, plasma 3-OH-butyrate, and cytokine concentrations were analyzed with the software package SPSS (version 12) using either one-way analysis of variance (ANOVA; factor treatment), two-way ANOVA (factors trait×treatment) or two-way ANOVA for repeated measures (factors trait×treatment×stimulus) followed by a Bonferroni post hoc test for multiple comparisons when appropriate. For analysis of cytokine concentrations, a Mann–Whitney U-test was applied (for detailed statistical analysis see Supplementary Table S2 as well as figure descriptions; for detailed group sizes see Supplementary Table S2). Group sizes were defined by power analysis and experimental experience. Animals were excluded from statistical analysis, if the respective parameter differed more than twice the standard deviation from the group mean. For microbiome data, the observed OTU numbers, 16S-rDNA copy numbers, and relative abundances of bacterial taxa were analyzed in R by ANOVA with a subsequent Tukey’s test. Pairwise multilevel comparisons of Bray–Curtis distances as depicted in the PCoA plot were analyzed using the vegan package in R followed by a Bonferroni correction to adjust p values. Correlations between bacterial families and plasma butyrate were calculated using Spearman’s correlation coefficients in GraphPad Prism (version 5). Significance was accepted at p ≤ 0.05.
Behavioral effects of minocycline in the SPT, LDB, EPM, and FST
Male and female HAB and NAB rats were treated with either minocycline (40 mg/kg), escitalopram or a combination of both via the drinking water for 22 days, and fluid intake was monitored daily (see supplementary results Table S3 and Fig. S1). In the SPT, all rats displayed natural social preference as indicated by a higher investigation time of the social versus the non-social stimulus (p < 0.001; Fig. 1b–e). Post hoc analyses revealed that minocycline alone facilitated social approach in male (Fig. 1b) and female (Fig. 1c) HAB rats (p < 0.05 vs. Veh). In both the LDB and EPM, the expected anxious phenotype of HAB rats was visible in both sexes compared to NAB rats (p < 0.05; Fig. S2). A treatment effect was only seen in male NAB rats, where escitalopram alone increased the time in the light box (p < 0.05).
Concomitant with the high anxiety phenotype, male and female HAB rats displayed reduced struggling and increased immobility in the FST compared to NABs (p < 0.001; Fig. 1f–i). Minocycline was the only treatment that reversed this phenotype, but exclusively in male HAB rats indicated by decreased immobility and increased struggling (p < 0.05 vs. Veh, Fig. 1f, h). No treatment-induced changes in locomotion in HAB rats (Fig. S2) and no influence of the female cycle on behavior was detectable (data not shown).
To assess potential sex-dependent differences in effective doses, 80 mg/kg minocycline was also administered to male and female HAB rats. Again, minocycline increased social preference in both sexes (p < 0.001; Fig. S3A, B) and ameliorated depressive-like behavior in male HAB rats (p < 0.05; Fig. S3G–J), whereas anxiety-like behavior remained unchanged (Fig. S3C–F). Hence, in all following analysis, only samples from the 40 mg/kg groups were analyzed.
Effects of minocycline on microglial numbers in the PFC and cytokine concentrations in plasma
The effects of minocycline, escitalopram, or the combination on microglial quantity in infralimbic/prelimbic PFC slices were assessed using Iba-1 as a marker of both resting and reactive microglia. In male (p < 0.001; Fig. 2a) and female (p < 0.01; Fig. 2b) HAB rats, overall lower counts of microglia cells were detected compared to NAB rats. A treatment effect was seen exclusively in male HAB rats with post hoc analysis revealing further reduced microglial numbers after minocycline treatment (p < 0.05; Fig. 2a). As only male HAB rats responded both behaviorally and in microglial numbers to minocycline, all subsequent analyses, i.e. of peripheral pro-inflammatory cytokine concentrations and microbiome composition, were performed exclusively in minocycline-treated male HAB vs. NAB rats. Minocycline reduced IFN-γ levels in male HAB and NAB rats (p < 0.05; Fig. 3a), whereas IL-12 subunit p40 levels remained unchanged (Fig. 3b).
Distribution of minocycline in liver and fecal boli
Minocycline was detectable in fecal boli suggesting its significant availability in the large intestine, including the cecum (Table 1). Comparable levels were found in the liver of both male and female rats irrespective of trait anxiety. This correlated with liquid (i.e. minocycline) intake on the last treatment day (data not shown).
Intestinal microbial composition
After 16S-rDNA-based high-throughput sequencing, analysis revealed comparable total bacterial 16S-rDNA copy numbers and microbial richness, represented by OTU counts, in HAB and NAB rats, which was reduced by minocycline in both lines (p < 0.01; Fig. 4a, b). The overall composition of cecal microbiota, as assessed by principal coordinates analysis of Bray–Curtis distances (beta-diversity), revealed marked differences between HAB and NAB rats shown by four distinct clusters corresponding to the two treatment conditions (p = 0.012; Fig. 4c). This analysis clearly shows a strong perturbation of the gut microbiota as a response to minocycline application in both rat lines and diminished differences between HABs and NABs following treatment.
In detail, striking differences between HAB and NAB rats were identified regarding the highly prevalent Lachnospiraceae family of the Clostridiales order (p < 0.05; Fig. 4d). Minocycline treatment elevated the lower frequency in HABs to the level of NABs that — in terms of this family — were not affected by treatment. Further, a relative increase in the abundance of the Clostridiales Family XIII in both lines was observed after minocycline (p < 0.01; Fig. 4e). Interestingly, many Lachnospiraceae members as well as a number of Clostridiales Family XIII strains have been implicated in the production of butyrate that exerts important pleiotropic functions in the intestinal tract and beyond49. Consistently, we found significantly augmented levels of 3-OH-butyrate after minocycline treatment in both lines that was even higher in HAB compared to NAB rats (p < 0.05; Fig. 4f). Spearman’s rank analysis disclosed positive correlations between 3-OH-butyrate levels and abundance of the two mentioned Clostridiales families in individual HAB rats corroborating an important contribution of the respective bacteria to systemic butyrate availability (p < 0.001; Fig. 4g, i). In NAB rats, minocycline-induced augmentation of the Family XIII population, but not of Lachnospiraceae, positively correlated with 3-OH-butyrate levels (p < 0.001; Fig. 4h, j), which presumably accounted for the moderate increase in 3-OH-butyrate concentrations of NABs.
In the present study, we confirm the antidepressant effect of minocycline and reveal that chronic minocycline treatment reduces depressive-, but not anxiety-like, behavior and affects the gut–brain axis in a sex- and trait anxiety-dependent manner. These findings extend previous reports of antidepressant actions of minocycline18,20,25,26,28,50 to male rats with high levels of innate anxiety- and depressive-like behavior. In addition, chronic minocycline facilitated social preference behavior in HAB males and females as indicated in previous studies25,51,52. However, as HAB rats generally do not show impairments in social interaction, the elevated social preference rather seems to reflect an alleviation of depressive-like behavior36,53 than an improvement in social approach per se. Interestingly, we could not replicate the proposed anxiolytic-like effect of minocycline17,50 either in HAB or NAB rats. Thus, it appears that anxiety-like behavior in HAB rats is manifested via a mechanism independent of the inflammatory system or any other target of minocycline33,54. Importantly, the antidepressant effect of minocycline was not observed in female HAB rats. Similarly, minocycline was able to abolish inflammatory neuropathic pain55 and improved morphine-induced analgesia56 only in male mice, proposing a sex-specificity of its actions. Of note, we carefully considered an influence of repeated testing57,58 on the behavioral effects of minocycline and, accordingly, the least stressful test (SPT) was performed first, and the most stressful test (FST) last, with a full day of rest between two tests to avoid stress- or experience-induced bias.
Chronic escitalopram59 or citalopram60 treatment has been described to ameliorate chronic stress-induced depressive-like behavior in both rats and mice, and citalopram and paroxetine given over 8 weeks have also been proven to be effective in HAB males34,35. In the present study we could only reproduce the anxiolytic effect of escitalopram in male NAB rats in the LDB, but not in HAB or female rats, probably due to the short treatment time. Importantly, these results support a sex difference in treatment strategies for MDD and validate the HAB breeding line as a model for innate treatment-resistant depressive-like behavior with minocycline as a potential treatment.
Clinical studies provide growing evidence for an increased efficacy of adjunctive treatment in MDD5. Fittingly, minocycline treatment, in combination with several conventional antidepressants like SSRIs or antipsychotics, improved MDD symptoms19,20,21. However, a study in depressed patients revealed that administration of citalopram in combination with a non-steroidal anti-inflammatory drug inhibited remission61. In keeping, in the present study 3-week treatment with minocycline together with escitalopram abolished the antidepressant effect of minocycline. In agreement with our results, minocycline in combination with the SSRI fluoxetine, but not the tricyclic desipramine, prevented the antidepressant effects of minocycline in rats23,24. Together, these findings strongly suggest that minocycline specifically counteracts a mechanism responsible for the antidepressant-like effect of SSRIs. Though minocycline interferes with the effectiveness of escitalopram in this case, it does not necessarily target the monoaminergic mode of action, but might target substance-specific secondary mechanisms or elicit local pharmacokinetic interactions.
Minocycline has been repeatedly demonstrated to inhibit microglial activity and proliferation accompanying its effects on behavior16,17,26,28,43,50,62,63 and - as an antibiotic - to modulate the gut microbial composition18. Neuroinflammation and increased microglial activation have been associated with MDD8,27,43,64,65. However, a dynamic and bi-directional alteration in microglial status has recently been hypothesized to underlie depressive-like behavior, as microglial numbers were found to be initially elevated followed by their decline in the hippocampus and PFC of chronically stressed rodents that displayed depressive-like behavior51. The lower microglial density in the PFC of HAB rats is likely due to their permanent stress state, as shown by elevated trait anxiety and a hyper-reactive HPA axis66. Interestingly, administration of minocycline further reduced microglial numbers, specifically in male HAB rats, which paralleled the antidepressant-like behavioral effect. Similar to a reduction in microglia, acute inhibition of the infralimbic cortex in male HAB rats led to an antidepressant-like phenotype39, indicating the PFC to be involved in depressive-like behavior in male HAB rats. Minocycline has been shown to inhibit microglial proliferation17,67 and, in view of a constant rate of microglial apoptosis68, should therefore lead to a further reduced microglial density in male HAB rats. Although the underlying mechanisms of the dynamic interplay between proliferation and apoptosis need to be explored in more detail, our results point towards an impaired microglial homeostasis and functioning as an underlying mechanism for the depressive-like behavior in HAB rats, and further support our breeding line as a model for inflammation-associated depressive-like behavior. Of note, the reduction in microglial numbers by minocycline was abolished, when given in combination with escitalopram.
The microbiome-gut–brain axis has been shown to modulate microglia proliferation and maturation. For example, phenotypical abnormalities of microglia found in germ-free mice were reversed by a microbiota-derived short-chain fatty acid mixture containing butyrate12. Gut microbiota dysbiosis, in turn, can result in neuroinflammation by chronic activation of microglia in the CNS69, potentially contributing to the behavioral phenotype in HAB rats. Supporting the link between the microbiome and emotional behavior6,9,70, HAB and NAB rats originating from the same breeding facility show - despite comparable total bacterial numbers in their cecal contents - profound differences in global gut microbiota composition, reflecting the robust behavioral differences between the two lines. As expected, 3 weeks of minocycline treatment reduced bacterial richness similarly in both groups resulting in still persisting, but diminished group differences. This suggests a partial equalization of the microbiota between both lines that might contribute to the observed antidepressant-like effect of minocycline in HAB rats. Interestingly, in patients suffering from MDD, an altered microbial composition was observed that induced similar symptoms in rats upon transplantation71,72.
Importantly, detailed microbiome comparison between HAB and NAB rats revealed decreased relative abundance of the Lachnospiraceae family in HABs, which expanded after minocycline treatment. Similar dynamic changes in Lachnospiraceae were found in a stress model of depression18. We further show that minocycline elevated relative Clostridiales Family XIII levels in both HAB and NAB rats. Both Lachnospiraceae and Clostridiales Family XIII accommodate a large part of butyrate-producing bacterial genera, reflected by increased plasma 3-OH-butyrate levels especially in HAB, but also in NAB rats, after minocycline. In support, a positive correlation between the abundance of Lachnospiraceae, as well as the Clostridiales Family XIII, with 3-OH-butyrate was found in male HAB rats. In contrast, in male NABs a positive correlation was only found with Clostridiales Family XIII. Both butyrate and 3-OH-butyrate have been proposed as anti-inflammatory agents that execute their effects via inhibition of peripheral T cell activity73 and microglia activation74, and even via inducing microglial apoptosis75. In line, minocycline decreased the level of the pro-inflammatory cytokine IFN-γ, produced by IL-12-induced and activated T-helper type 1 cells76, in both HAB and NAB males. Plasma levels of IL-12p40 appeared to be higher in HAB rats and were reduced by minocycline to NAB levels, supporting a regulatory role of minocycline and butyrate on peripheral T cells73,77 independent of the central immune system that might contribute to the antidepressant effect of minocycline. Although a role of butyrate in the regulation of the central immune system remains to be studied, our results suggest that butyrate-mediated microglial apoptosis75 might contribute to the observed reduction in microglial density in the PFC of male HAB rats. Furthermore, butyrate has been shown to exert antidepressant-like effects in mice78,79 and rats80. These findings point towards an important role of bacteria-produced butyrate as a mediator of behavioral and microglial alterations in minocycline-treated HAB rats. Thus, our results support the hypothesis of an influence of the gut microbiome on anxiety- and depressive-like behavior in our rodent model of anxiety and depression.
In summary, we show that the depressive- and anxiety-like phenotype of HAB rats is accompanied by reduced microglial numbers in the infralimbic/prelimbic PFC and a distinct shift of the gut-bacterial composition. This emphasizes that HAB rats are a valid model for inflammation-associated depressive-like behavior and points towards a complex interplay between microbiota/microbial metabolites and the immune system, as proposed by the concept of the microbiota-gut–brain axis.
In the course of clinical application, the present results indicate that promoting an anti-inflammatory state by control of microglial activation and/or modulation of the gut microbiome and metabolome, as shown after prolonged minocycline treatment, offers promising potential as a therapeutic strategy in treatment-resistant MDD. The present study was designed to detect an early response (3 weeks) to minocycline and did not mimic a clinical antidepressant treatment. Thus, a longer treatment duration might reveal different effects. Nevertheless, caution is needed when considering minocycline as an augmentation strategy of SSRIs like escitalopram, especially in the absence of a pro-inflammatory profile, which may explain some of the recent high-profile clinical failures of minocycline.
World Health Organization. Depression and other common mental disorders: global health estimates. 2017.
Burke, W. J. Escitalopram. Expert Opin. Invest. Drugs 11, 1477–1486 (2002).
Murdoch, D. & Keam, S. J. Escitalopram: a review of its use in the management of major depressive disorder. Drugs 65, 2379–2404 (2005).
Cryan, J. & Slattery, D. Animal models of mood disorders: recent developments. Curr. Opin. Psychiatry 20, 1–7 (2007).
Ceskova, E. & Silhan, P. Novel treatment options in depression and psychosis. Neuropsychiatr. Dis. Treat. 14, 741–747 (2018).
Dinan, T. G. & Cryan, J. F. Brain-gut-microbiota axis and mental health. Psychosom. Med. 79, 920–926 (2017).
Köhler, O., Krogh, J., Mors, O. & Eriksen Benros, M. Inflammation in depression and the potential for anti-inflammatory treatment. Curr. Neuropharmacol. 14, 732–742 (2016).
Yirmiya, R., Rimmerman, N. & Reshef, R. Depression as a microglial disease. Trends Neurosci. 38, 637–658 (2015).
Dinan, T. G. & Cryan, J. F. Melancholic microbes: a link between gut microbiota and depression? Neurogastroenterol. Motil. 25, 713–719 (2013).
Torres-Platas, S. G., Cruceanu, C., Chen, G. G., Turecki, G. & Mechawar, N. Evidence for increased microglial priming and macrophage recruitment in the dorsal anterior cingulate white matter of depressed suicides. Brain Behav. Immun. 42, 50–59 (2014).
Lach, G., Schellekens, H., Dinan, T. G. & Cryan, J. F. Anxiety, depression, and the microbiome: a role for gut peptides. Neurotherapeutics 15, 36–59 (2018).
Erny, D. et al. Host microbiota constantly control maturation and function of microglia in the CNS. Nat. Neurosci. 18, 965–977 (2015).
Matcovitch-Natan, O. et al. Microglia development follows a stepwise program to regulate brain homeostasis. Science (80-) 353, aad8670 (2016).
Wu, D. C. et al. Blockade of microglial activation is neuroprotective in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine mouse model of Parkinson disease. J. Neurosci. 22, 1763–1771 (2002).
Choi, Y. et al. Minocycline attenuates neuronal cell death and improves cognitive impairment in Alzheimer’s disease models. Neuropsychopharmacology 32, 2393–2404 (2007).
Yrjänheikki, J., Keinänen, R., Pellikka, M., Hökfelt, T. & Koistinaho, J. Tetracyclines inhibit microglial activation and are neuroprotective in global brain ischemia. Proc. Natl Acad. Sci. USA 95, 15769–15774 (1998).
Soczynska, J. K. et al. Novel therapeutic targets in depression: minocycline as a candidate treatment. Behav. Brain Res. 235, 302–317 (2012).
Wong, M.-L. et al. Inflammasome signaling affects anxiety- and depressive-like behavior and gut microbiome composition. Mol. Psychiatry 21, 797–805 (2016).
Dean, O. M. et al. Adjunctive minocycline treatment for major depressive disorder: A proof of concept trial. Aust. N. Z. J. Psychiatry 51, 829–840 (2017).
Rosenblat, J. D. & McIntyre, R. S. Efficacy and tolerability of minocycline for depression: a systematic review and meta-analysis of clinical trials. J. Affect. Disord. 227, 219–225 (2017).
Husain, M. I. et al. Minocycline as an adjunct for treatment-resistant depressive symptoms: A pilot randomised placebo-controlled trial. J. Psychopharmacol. 31, 1166–1175 (2017).
Deakin, B. et al. The benefit of minocycline on negative symptoms of schizophrenia in patients with recent-onset psychosis (BeneMin): a randomised, double-blind, placebo-controlled trial. The Lancet Psychiatry 5, 885–894 (2018).
Molina-Hernández, M., Téllez-Alcántara, N. P., Pérez-García, J., Olivera-Lopez, J. I. & Jaramillo-Jaimes, M. T. Desipramine or glutamate antagonists synergized the antidepressant-like actions of intra-nucleus accumbens infusions of minocycline in male Wistar rats. Prog. Neuropsychopharmacol. Biol. Psychiatry 32, 1660–1666 (2008).
Molina-Hernández, M., Tellez-Alcántara, N. P., Pérez-García, J., Olivera-Lopez, J. I. & Jaramillo-Jaimes, M. T. Antidepressant-like actions of minocycline combined with several glutamate antagonists. Prog. Neuropsychopharmacol. Biol. Psychiatry 32, 380–386 (2008).
Henry, C. J. et al. Minocycline attenuates lipopolysaccharide (LPS)-induced neuroinflammation, sickness behavior, and anhedonia. J. Neuroinflammation 5, 15 (2008).
Zheng, L.-S., Kaneko, N. & Sawamoto, K. Minocycline treatment ameliorates interferon-alpha- induced neurogenic defects and depression-like behaviors in mice. Front. Cell. Neurosci. 9, 1–10 (2015).
Burke, N. N., Kerr, D. M., Moriarty, O., Finn, D. P. & Roche, M. Minocycline modulates neuropathic pain behaviour and cortical M1-M2 microglial gene expression in a rat model of depression. Brain Behav. Immun. 42, 147–156 (2014).
Wang, H. T. et al. Early-life social isolation-induced depressive-like behavior in rats results in microglial activation and neuronal histone methylation that are mitigated by minocycline. Neurotox. Res 31, 505–520 (2017).
Toth, I., Neumann, I. D. & Slattery, D. A. Social fear conditioning: a novel and specific animal model to study social anxiety disorder. Neuropsychopharmacology 37, 1433–1443 (2012).
Liebsch, G., Montkowski, A., Holsboer, F. & Landgraf, R. Behavioural profiles of two Wistar rat lines selectively bred for high or low anxiety-related behaviour. Behav. Brain Res. 94, 301–310 (1998).
Landgraf, R. Wigger a. Born to be anxious: neuroendocrine and genetic correlates of trait anxiety in HAB rats. Stress 6, 111–119 (2003).
Keck, M. E. et al. Differences in serotonergic neurotransmission between rats displaying high or low anxiety/depression-like behaviour: effects of chronic paroxetine treatment. J. Neurochem. 92, 1170–1179 (2005).
Wegener, G., Mathe, A. A. & Neumann, I. D. Selectively bred rodents as models of depression and anxiety. Curr. Top. Behav. Neurosci. 12, 139–187 (2012).
Jochum, T. et al. Decreased sensitivity to thermal pain in rats bred for high anxiety-related behaviour is attenuated by citalopram or diazepam treatment. Behav. Brain Res. 183, 18–24 (2007).
Keck, M. E. et al. Reduction of hypothalamic vasopressinergic hyperdrive contributes to clinically relevant behavioral and neuroendocrine effects of chronic paroxetine treatment in a psychopathological rat model. Neuropsychopharmacology 28, 235–243 (2003).
Krishnan, V. & Nestler, E. J. The molecular neurobiology of depression. Nature 455, 894–902 (2008).
Berton, O. & Nestler, E. J. New approaches to antidepressant drug discovery: beyond monoamines. Nat. Rev. Neurosci. 7, 137–151 (2006).
Drevets, W. C. Neuroimaging and neuropathological studies of depression: implications for the cognitive- emotional features of mood disorders. Curr. Opin. Neurobiol. 11, 240–249 (2001).
Slattery, D. A., Neumann, I. D. & Cryan, J. F. Transient inactivation of the infralimbic cortex induces antidepressant-like effects in the rat. J. Psychopharmacol. 25, 1295–1303 (2011).
Harrison, P. J. The neuropathology of primary mood disorder. Brain 125, 1428–1449 (2002).
Gasull-Camós, J., Tarrés-Gatius, M., Artigas, F. & Castañé, A. Glial GLT-1 blockade in infralimbic cortex as a new strategy to evoke rapid antidepressant-like effects in rats. Transl. Psychiatry 7, e1038 (2017).
Banasr, M. & Duman, R. S. Glial loss in the prefrontal cortex is sufficient to induce depressive-like behaviors. Biol. Psychiatry 64, 863–870 (2008).
Hinwood, M., Morandini, J., Day, T. A. & Walker, F. R. Evidence that microglia mediate the neurobiological effects of chronic psychological stress on the medial prefrontal cortex. Cereb. Cortex 22, 1442–1454 (2012).
Mayberg, H. S. et al. Deep brain stimulation for treatment-resistant depression. Neuron 45, 651–660 (2005).
Landgraf, R. & Wigger, A. High vs low anxiety-related behavior rats: an animal model of extremes in trait anxiety. Behav. Genet. 32, 301–314 (2002).
Kilkenny, C., Browne, W. J., Cuthill, I. C., Emerson, M. & Altman, D. G. Improving bioscience research reporting: the arrive guidelines for reporting animal research. PLoS Biol. 8, e1000412 (2010).
Jayatissa, M. N., Bisgaard, C., Tingström, A., Papp, M. & Wiborg, O. Hippocampal cytogenesis correlates to escitalopram-mediated recovery in a chronic mild stress rat model of depression. Neuropsychopharmacology 31, 2395–2404 (2006).
Frazer, A. & Morilak, D. A. What should animal models of depression model? Neurosci. Biobehav. Rev. 29, 515–523 (2005).
Louis, P. & Flint, H. J. Diversity, metabolism and microbial ecology of butyrate-producing bacteria from the human large intestine. FEMS Microbiol. Lett. 294, 1–8 (2009).
Wang, Y.-L. et al. Microglial activation mediates chronic mild stress-induced depressive- and anxiety-like behavior in adult rats. J. Neuroinflammation 15, 21 (2018).
Kreisel, T. et al. Dynamic microglial alterations underlie stress-induced depressive-like behavior and suppressed neurogenesis. Mol. Psychiatry 19, 699–709 (2014).
Zhu, F. et al. Minocycline and risperidone prevent microglia activation and rescue behavioral deficits induced by neonatal intrahippocampal injection of lipopolysaccharide in rats. PLoS ONE 9, e93966 (2014).
Krishnan, V. et al. Molecular adaptations underlying susceptibility and resistance to social defeat in brain reward regions. Cell 131, 391–404 (2007).
Slattery, D. A. et al. Selective breeding for high anxiety introduces a synonymous SNP that increases neuropeptide S receptor activity. J. Neurosci. 35, 4599–4613 (2015).
Chen, G., Luo, X., Qadri, M. Y., Berta, T. & Ji, R.-R. Sex-dependent glial signaling in pathological pain: distinct roles of spinal microglia and astrocytes. Neurosci. Bull. 34, 98–108 (2018).
Posillico, C. K., Terasaki, L. S., Bilbo, S. D. & Schwarz, J. M. Examination of sex and minocycline treatment on acute morphine-induced analgesia and inflammatory gene expression along the pain pathway in Sprague-Dawley rats. Biol. Sex Differ. 6, 1–12 (2015).
Bouwknecht, J. A., Van Der Gugten, J., Groenink, L., Olivier, B. & Paylor, R. E. Effects of repeated testing in two inbred strains on flesinoxan dose-response curves in three mouse models for anxiety. Eur. J. Pharmcol. 494, 35–44 (2004).
McIlwain, K. L., Merriweather, M. Y., Yuva-Paylor, L. A. & Paylor, R. The use of behavioral test batteries: effects of training history. Physiol. Behav. 73, 705–717 (2001).
Montgomery, S. A., Loft, H., Sánchez, C., Reines, E. H. & Papp, M. Escitalopram (S-Enantiomer of Citalopram): clinical efficacy and onset of action predicted from a rat model. Pharmacol. Toxicol. 88, 282–286 (2001).
Rygula, R. et al. Citalopram counteracts depressive-like symptoms evoked by chronic social stress in rats. Behav. Pharmacol. 17, 19–29 (2006).
Warner-Schmidt, J. L., Vanover, K. E., Chen, E. Y., Marshall, J. J. & Greengard, P. Antidepressant effects of selective serotonin reuptake inhibitors (SSRIs) are attenuated by antiinflammatory drugs in mice and humans. Proc. Natl Acad. Sci. USA 108, 9262–9267 (2011).
Du, Y. et al. Minocycline prevents nigrostriatal dopaminergic neurodegeneration in the MPTP model of Parkinson’s disease. Proc. Natl Acad. Sci. USA 98, 14669–14674 (2001).
Xu, N. et al. Spared nerve injury increases the expression of microglia M1 markers in the prefrontal cortex of rats and provokes depression-like behaviors. Front. Neurosci. 11, 1–12 (2017).
Dheen, S. T., Kaur, C. & Ling, E.-A. Microglial activation and its implications in the brain diseases. Curr. Med. Chem. 14, 1189–1197 (2007).
Dantzer, R., O’Connor, J. C., Freund, G. G., Johnson, R. W. & Kelley, K. W. From inflammation to sickness and depression: when the immune system subjugates the brain. Nat. Rev. Neurosci. 9, 46–56 (2008).
Landgraf, R., Wigger, A., Holsboer, F. & Neumann, I. D. Hyper-reactive hypothalamo-pituitary-adrenocortical axis in rats bred for high anxiety-related behaviour. J. Neuroendocrinol. 11, 405–407 (1999).
Tikka, T., Fiebich, B. L., Goldsteins, G., Keinanen, R. & Koistinaho, J. Minocycline, a tetracycline derivative, is neuroprotective against excitotoxicity by inhibiting activation and proliferation of microglia. J. Neurosci. 21, 2580–2588 (2001).
Gehrmann, J. & Banati, R. B. Microglial turnover in the injured CNS: activated microglia undergo delayed DNA fragmentation following peripheral nerve injury. J. Neuropathol. Exp. Neurol. 54, 680–688 (1995).
Kim, J. S. & de La Serre, C. B. Diet, gut microbiota composition and feeding behavior. Physiol. Behav. 192, 177–181 (2018).
Cryan, J. F. & Dinan, T. G. Mind-altering microorganisms: the impact of the gut microbiota on brain and behaviour. Nat. Rev. Neurosci. 13, 701–712 (2012).
Jiang, H. et al. Altered fecal microbiota composition in patients with major depressive disorder. Brain Behav. Immun. 48, 186–194 (2015).
Kelly, J. R. et al. Transferring the blues: depression-associated gut microbiota induces neurobehavioural changes in the rat. J. Psychiatr. Res. 82, 109–118 (2016).
Kim, C. H., Park, J. & Kim, M. Gut microbiota-derived short-chain fatty acids, T cells, and inflammation. Immune Netw. 14, 277 (2014).
Fu, S. P. et al. Anti-inflammatory effects of BHBA in both in vivo and in vitro Parkinson’s disease models are mediated by GPR109A-dependent mechanisms. J. Neuroinflammation 12, 1–14 (2015).
Chen, P. S. et al. Valproic acid and other HDAC inhibitors induce microglial apoptosis and attenuate lipopolysaccharide- induced dopaminergic neurotoxicity. Neuroscience 149, 203–212 (2007).
Croxford, A. L., Kulig, P. & Becher, B. IL-12-and IL-23 in health and disease. Cytokine Growth Factor Rev. 25, 415–421 (2014).
Giuliani, F., Hader, W. & Yong, V. W. Minocycline attenuates T cell and microglia activity to impair cytokine production in T cell-microglia interaction. J. Leukoc. Biol. 78, 135–143 (2005).
Resende, W. R. et al. Effects of sodium butyrate in animal models of mania and depression: implications as a new mood stabilizer. Behav. Pharmacol. 24, 569–579 (2013).
Valvassori, S. et al. Sodium butyrate, a histone deacetylase inhibitor, reverses behavioral and mitochondrial alterations in animal models of depression induced by early- or late-life stress. Curr. Neurovasc. Res. 12, 312–320 (2015).
Wei, Y. et al. effect of sodium butyrate is associated with an increase in tet1 and in 5-hydroxymethylation levels in the Bdnf gene. Int. J. Neuropsychopharmacol. 18, 1–10 (2015).
We thank Lundbeck A/S (Copenhagen, Denmark) for generously providing Escitalopram oxalate. We thank Martina Toelge (Microbiomix, Regensburg, Germany) for performance and validation of the Luminex cytokine assay. Further, we thank Helena Kummer, Sang-Yi Go, Finn Hartmann, and Teresa Mayer for excellent experimental support and Andrea Havasi, Rodrigue Maloumby, Nadja Reul and Chrisine Irtenkauf for excellent technical assistance. This work was supported by the German Federal Ministry of Education and Research (Bundesministerium für Bildung und Forschung, BMBF), Research Grants No. 01EE1401A and 01EE1401B.
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Schmidtner, A.K., Slattery, D.A., Gläsner, J. et al. Minocycline alters behavior, microglia and the gut microbiome in a trait-anxiety-dependent manner. Transl Psychiatry 9, 223 (2019). https://doi.org/10.1038/s41398-019-0556-9
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