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Dietary interventions with n-3 fatty acids or probiotics targeting post-myocardial infarction depression

Published online by Cambridge University Press:  03 January 2013

Rafat A. Siddiqui
Affiliation:
Cellular Biochemistry Laboratory, Methodist Research Institute, Indiana University Health, Indiana University School of Medicine, Indianapolis, IN46202, USA email: [email protected]
Kevin A. Harvey
Affiliation:
Cellular Biochemistry Laboratory, Methodist Research Institute, Indiana University Health, Indiana University School of Medicine, Indianapolis, IN46202, USA email: [email protected]
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Abstract

Type
Invited Commentary
Copyright
Copyright © The Authors 2012

In this issue of the British Journal of Nutrition, Gilbert et al. (Reference Gilbert, Arseneault-Bréard and Monaco1) describe attenuation of post-myocardial infarction (MI) depression by dietary supplementation with n-3 fatty acids or probiotics in a rat model. This paper indicates the importance of dietary intervention to avoid post-MI depression. Previously, it was shown that a high-PUFA diet enriched with n-3 fatty acids or a low-PUFA diet enriched with probiotics (Lactobacillus helveticus R0052 and Bifidobacterium longum R0175), when fed before the ischaemic period, reduced apoptosis in the limbic system of the brain and reduced circulating pro-inflammatory cytokines(Reference Girard, Bah and Kaloustian2, Reference Rondeau, Picard and Bah3). This recent study further demonstrates that a diet containing either high n-3 PUFA or probiotics, when given after the onset of ischaemia/reperfusion, is also able to inhibit apoptosis in the limbic system, reduce circulating levels of pro-inflammatory cytokines and attenuate post-MI depression. These studies indicate that n-3 fatty acids or probiotics may be very useful dietary components in attenuating post-MI depression.

Depression is a common symptom of MI(Reference Ziegelstein4). Approximately 10–50 % of all MI patients show symptoms of depression with variable severity(Reference Bush, Ziegelstein and Patel5); however, approximately one in six patients with MI experience major depression(Reference Frasure-Smith, Lesperance and Talajic6Reference Schleifer, Macari-Hinson and Coyle8). The common symptoms are depressed mood, diminished interest or pleasure and low self-esteem. Some patients exhibit these symptoms at initial hospitalisation, whereas in others depression may occur during recovery from MI or 1–4 months post-MI(Reference Bush, Ziegelstein and Patel5). Patients with depression are likely to be non-compliant with medical treatment regimens(Reference DiMatteo, Lepper and Croghan9, Reference Carney, Freedland and Eisen10) and have a greater dropout rate from cardiac rehabilitation programmes(Reference Blumenthal, Williams and Wallace11). Post-MI depression is often associated with cardiac readmission and a poor quality of life during the first year, with a significantly increased risk of subsequent death(Reference van Melle, de Jonge and Spijkerman12). Post-MI depression is an independent risk factor for increased mortality. Patients with post-MI depressive disorder carry a 2·0- to 2·5-fold increase in the relative risk of new cardiovascular events and cardiac mortality(Reference van Melle, de Jonge and Spijkerman12). Furthermore, they incur high costs for health care services due to hospital readmission. Although controversial, patients with major depression have been shown to have decreased brain serotonin (5-hydroxytryptamine) activity(Reference Lacasse and Leo13). Serotonin metabolism in the central nervous system is influenced by pro-inflammatory cytokines(Reference Schiepers, Wichers and Maes14); IL-1, interferon (IFN)-α, IFN-γ and TNF-α all up-regulate the serotonin transporter, thus causing a depletion of extracellular serotonin, whereas IL-4 (an anti-inflammatory cytokine) reduces serotonin uptake(Reference Schiepers, Wichers and Maes14Reference Mossner, Daniel and Schmitt16). It is interesting that Gilbert et al. (Reference Gilbert, Arseneault-Bréard and Monaco1) demonstrated lower concentrations of plasma monocyte chemoattractant protein-1, a pro-inflammatory cytokine, on the high-n-3 PUFA diet and an increase in IL-4, an anti-inflammatory cytokine, on the probiotic diet. Although this study did not monitor serotonergic activity, inhibition of apoptosis in the dentate gyrus and the medial amygdala suggests that cytokines play an important role in the attenuation of post-MI depression. Inhibition of pro-inflammatory cytokines is not only beneficial for attenuating depressive symptoms, but may also help to reduce the inflammation caused by MI.

A growing number of studies support a role for n-3 fatty acids in depression and neuropsychiatric dysfunction. Depressed patients have significantly depleted total n-3 PUFA and DHA in serum and erythrocyte membranes(Reference Peet, Murphy, Shay and Horrobin17, Reference Maes, Christophe and Delanghe18). In cross-sectional investigations, infrequent or reduced fish consumption was independently associated with depressive symptoms and a higher rate of depression, whereas higher fish consumption was well correlated with a lower prevalence of major depression(Reference Hibbeln19, Reference Hibbeln20). Other studies have shown that increased seafood consumption is also predictive of reduced postpartum depression and bipolar disorders(Reference Noaghiul and Hibbeln21). The n-3 fatty acids, EPA and DHA, can mediate anti-depressive effects through multiple mechanisms. n-3 Fatty acids are incorporated into all cell membranes, especially those of the brain and myocardium. These fatty acids are known to assist in nerve cell signalling and neurodevelopment. n-3 PUFA regulate serotonergic and dopaminergic neurotransmitters and thereby have a direct effect on depressive symptoms(Reference Hibbeln and Salem22, Reference Horrobin and Bennett23). Furthermore, these fatty acids also provide beneficial effects to MI patients by modulating the activities of cardiac ion-channel proteins(Reference Lombardi and Terranova24). In addition to this, n-3 fatty acids are well known for their anti-inflammatory properties. The anti-inflammatory effects of n-3 fatty acids are mediated through their effects on arachidonic acid (AA) metabolism. AA serves as a precursor to inflammatory mediators such as thromboxanes, PG and leukotrienes. n-3 Fatty acids not only compete with AA for incorporation into cell membranes, but also compete (especially EPA) with AA for rate-limiting enzymes for the synthesis of the above-mentioned inflammatory mediators. Moreover, the anti-apoptotic properties of n-3 fatty acids may also improve depression via a neuroprotective mechanism. For example, DHA facilitates the activation and translocation of Akt, an anti-apoptotic protein(Reference Akbar, Calderon, Wen and Kim25), and induces the expression of the Bcl-2 anti-apoptotic protein in neuronal cells(Reference Sinha, Khare and Rai26). DHA also reduces the activation of caspase-3, a pro-apoptotic protein(Reference Suphioglu, De Mel and Kumar27). Furthermore, as mentioned by Gilbert et al. (Reference Gilbert, Arseneault-Bréard and Monaco1), DHA generates neuroprotectin D, a powerful anti-inflammatory mediator that activates pro-survival signals down-regulating apoptosis. The results reported by Gilbert et al. (Reference Gilbert, Arseneault-Bréard and Monaco1) showed a similar reduction in apoptosis and inhibition of caspase activity by a high-n-3 PUFA diet. Although the authors have not examined the potential mechanism of DHA in attenuating post-MI depression in their model, it is likely that n-3 fatty acids may be acting through multiple mechanisms. The outcome of this study by Gilbert et al. (Reference Gilbert, Arseneault-Bréard and Monaco1) is not surprising because the effects of n-3 fatty acids on inflammation and depression are well-documented; however, the effect of probiotics on attenuating post-MI depression is an interesting finding in this paper.

Probiotics are live organisms that colonise the gut following their oral consumption and consequently have a beneficial effect, either directly or indirectly via their metabolic products, on the overall health of the host. Probiotics transiently colonise the gut, where they increase their concentration and create a balance in the gut microbiota to the benefit of the host. As reviewed by Sherman et al. (Reference Sherman, Ossa and Johnson-Henry28), the common beneficial effects of probiotics include antimicrobial activity towards enteric pathogens, maintenance of immune homeostasis in the gut, stimulation of anti-inflammatory cytokine secretion and reduced secretion of pro-inflammatory cytokines and influence on the activity of genes to help fight disease. Recent studies have also found a probiotic link between the brain and the gut. The enteric nervous system, which is the intrinsic nervous system of the gastrointestinal tract, plays an important role at the brain–gut axis. The vagus nerve is the primary route that the gut bacteria use to transmit information to the brain. A probiotic (B. longum NCC3001) has been shown to help normalise anxiety-like behaviour in mice with infectious colitis(Reference Bercik, Park and Sinclair29). Another probiotic (L. rhamnosus) affects γ-aminobutyric acid in certain brain regions, reducing anxiety- and depression-related behaviours(Reference Bravo, Forsythe and Chew30). Gilbert et al. (Reference Gilbert, Arseneault-Bréard and Monaco1) provide further evidence of probiotic effects on the brain–gut axis. Their data clearly indicate that probiotics attenuated post-MI depression in rats by inhibiting apoptotic processes in the dentate gyrus and the medial amygdala of the limbic system. The effect of the probiotic was associated with an increased plasma concentration of the anti-inflammatory cytokine, IL-4. It is interesting to note that combining high n-3 PUFA and probiotics showed no further improvement in attenuation of the post-MI depression. The authors suggest involvement of common pathways or a plateau effect. It is possible that, perhaps, by combining an n-3 fatty acid with probiotics, an additive or synergetic effect can be achieved with lower concentrations of these agents.

The study performed by Gilbert et al. (Reference Gilbert, Arseneault-Bréard and Monaco1) has enormous translational potential. It remains to be seen if similar effects can be reproduced in patients with post-MI depression. Both n-3 fatty acids and probiotics are inexpensive natural substances that are largely devoid of any side effects, and they can be easily incorporated into the diets of patients who have had an MI. In addition, either n-3 fatty acids or probiotics, or their combination, can be used as an adjunctive treatment to other antidepressants, not only to treat post-MI depression, but to treat other conditions with depressive symptoms as well.

References

1Gilbert, K, Arseneault-Bréard, J, Monaco, FF, et al. (2012) Attenuation of post-myocardial infarction depression in rats by n-3 fatty acids or probiotics starting after the onset of reperfusion. Br J Nutr 109, 5057.Google Scholar
2Girard, SA, Bah, TM, Kaloustian, S, et al. (2009) Lactobacillus helveticus and Bifidobacterium longum taken in combination reduce the apoptosis propensity in the limbic system after myocardial infarction in a rat model. Br J Nutr 102, 14201425.Google Scholar
3Rondeau, I, Picard, S, Bah, TM, et al. (2011) Effects of different dietary omega-6/3 polyunsaturated fatty acids ratios on infarct size and the limbic system after myocardial infarction. Can J Physiol Pharmacol 89, 169176.Google Scholar
4Ziegelstein, RC (2001) Depression after myocardial infarction. Cardiol Rev 9, 4551.CrossRefGoogle ScholarPubMed
5Bush, DE, Ziegelstein, RC, Patel, UV, et al. (2005) Post-myocardial infarction depression. Evid Rep Technol Assess (Summ) 18.Google ScholarPubMed
6Frasure-Smith, N, Lesperance, F & Talajic, M (1995) Depression and 18-month prognosis after myocardial infarction. Circulation 91, 9991005.CrossRefGoogle ScholarPubMed
7Frasure-Smith, N, Lesperance, F & Talajic, M (1993) Depression following myocardial infarction. Impact on 6-month survival. JAMA 270, 18191825.Google Scholar
8Schleifer, SJ, Macari-Hinson, MM, Coyle, DA, et al. (1989) The nature and course of depression following myocardial infarction. Arch Intern Med 149, 17851789.Google Scholar
9DiMatteo, MR, Lepper, HS & Croghan, TW (2000) Depression is a risk factor for noncompliance with medical treatment: meta-analysis of the effects of anxiety and depression on patient adherence. Arch Intern Med 160, 21012107.CrossRefGoogle ScholarPubMed
10Carney, RM, Freedland, KE, Eisen, SA, et al. (1995) Major depression and medication adherence in elderly patients with coronary artery disease. Health Psychol 14, 8890.Google Scholar
11Blumenthal, JA, Williams, RS, Wallace, AG, et al. (1982) Physiological and psychological variables predict compliance to prescribed exercise therapy in patients recovering from myocardial infarction. Psychosom Med 44, 519527.Google Scholar
12van Melle, JP, de Jonge, P, Spijkerman, TA, et al. (2004) Prognostic association of depression following myocardial infarction with mortality and cardiovascular events: a meta-analysis. Psychosom Med 66, 814822.CrossRefGoogle ScholarPubMed
13Lacasse, JR & Leo, J (2005) Serotonin and depression: a disconnect between the advertisements and the scientific literature. PLoS Med 2, e392.Google Scholar
14Schiepers, OJ, Wichers, MC & Maes, M (2005) Cytokines and major depression. Prog Neuropsychopharmacol Biol Psychiatry 29, 201217.Google Scholar
15Dunn, AJ, Swiergiel, AH & de Beaurepaire, R (2005) Cytokines as mediators of depression: what can we learn from animal studies? Neurosci Biobehav Rev 29, 891909.CrossRefGoogle ScholarPubMed
16Mossner, R, Daniel, S, Schmitt, A, et al. (2001) Modulation of serotonin transporter function by interleukin-4. Life Sci 68, 873880.CrossRefGoogle ScholarPubMed
17Peet, M, Murphy, B, Shay, J & Horrobin, D (1998) Depletion of omega-3 fatty acid levels in red blood cell membranes of depressive patients. Biol Psychiatry 43, 315319.CrossRefGoogle ScholarPubMed
18Maes, M, Christophe, A, Delanghe, J, et al. (1999) Lowered omega3 polyunsaturated fatty acids in serum phospholipids and cholesteryl esters of depressed patients. Psychiatry Res 85, 275291.Google Scholar
19Hibbeln, JR (2002) Seafood consumption, the DHA content of mothers' milk and prevalence rates of postpartum depression: a cross-national, ecological analysis. J Affect Disord 69, 1529.CrossRefGoogle ScholarPubMed
20Hibbeln, JR (1998) Fish consumption and major depression. Lancet 351, 1213.CrossRefGoogle ScholarPubMed
21Noaghiul, S & Hibbeln, JR (2003) Cross-national comparisons of seafood consumption and rates of bipolar disorders. Am J Psychiatry 160, 22222227.CrossRefGoogle ScholarPubMed
22Hibbeln, JR & Salem, N Jr (1995) Dietary polyunsaturated fatty acids and depression: when cholesterol does not satisfy. Am J Clin Nutr 62, 19.Google Scholar
23Horrobin, DF & Bennett, CN (1999) Depression and bipolar disorder: relationships to impaired fatty acid and phospholipid metabolism and to diabetes, cardiovascular disease, immunological abnormalities, cancer, ageing and osteoporosis. Possible candidate genes. Prostaglandins Leukot Essent Fatty Acids 60, 217234.Google Scholar
24Lombardi, F & Terranova, P (2007) Anti-arrhythmic properties of N-3 poly-unsaturated fatty acids (n-3 PUFA). Curr Med Chem 14, 20702080.CrossRefGoogle ScholarPubMed
25Akbar, M, Calderon, F, Wen, Z & Kim, HY (2005) Docosahexaenoic acid: a positive modulator of Akt signaling in neuronal survival. Proc Natl Acad Sci U S A 102, 1085810863.Google Scholar
26Sinha, RA, Khare, P, Rai, A, et al. (2009) Anti-apoptotic role of omega-3-fatty acids in developing brain: perinatal hypothyroid rat cerebellum as apoptotic model. Int J Dev Neurosci 27, 377383.Google Scholar
27Suphioglu, C, De Mel, D, Kumar, L, et al. (2010) The omega-3 fatty acid, DHA, decreases neuronal cell death in association with altered zinc transport. FEBS Lett 584, 612618.Google Scholar
28Sherman, PM, Ossa, JC & Johnson-Henry, K (2009) Unraveling mechanisms of action of probiotics. Nutr Clin Pract 24, 1014.Google Scholar
29Bercik, P, Park, AJ, Sinclair, D, et al. (2011) The anxiolytic effect of Bifidobacterium longum NCC3001 involves vagal pathways for gut–brain communication. Neurogastroenterol Motil 23, 11321139.Google Scholar
30Bravo, JA, Forsythe, P, Chew, MV, et al. (2011) Ingestion of Lactobacillus strain regulates emotional behavior and central GABA receptor expression in a mouse via the vagus nerve. Proc Natl Acad Sci U S A 108, 1605016055.Google Scholar