Depression IS NOT necessarily “all in your head”
Depression may be caused by purely psychological issues such as grief, loss, and fear; research tells us these types of issues themselves can bring about physical problems including elevations in homocysteine, decrease in thyroid function, and a host of other problems requiring nutritional intervention. Depressive symptoms may signal underlying physical disorders or may be a common side effect of a medicine you’ve been taking.
A fact that receives too little attention is that feelings of sadness, being out of control of our lives, anxiety and fatigue are often triggered by purely physical causes. The Merck Manual for Healthcare Professionals acknowledges this, listing possible causes including diseases, endocrine imbalances, nutritional deficiencies, pathogens and endocrine issues. Unfortunately most conventional Western physicians ignore this advice and view depressive symptoms as a “mental disorder.” They try to suppress depressive feelings though drug treatments that for the most part create emotional numbness.
No one should suffer from unremitting depressive feelings. CHS recommends you see a qualified Psychologist as your first Mental Health Professional, and consider one of our natural support formulas, which are far safer than antidepressants and antipsychotics that are promoted on TV!
What can I do?
Western Medicine
Conventional Western Allopaths broadly consider depressive symptoms to be caused by a chemical imbalance, primarily involving serotonin. Antidepressants are seen as first line treatment (in the U.S. only), with increasing supplementation with antipsychotics such as Abilify. Both classes of drugs have a long list of common and often severe harmful effects. They have not been proven to work, and are known to worsen depression in up to 8% of recipients. CHS recommends you AVOID “anti”depressants and antipsychotic drugs. Research has shown them to be ineffective for all but the most severe cases of depression, and benefits even then are lacking adequate scientific justification. If you have been taking these chemicals routinely DO NOT stop without professional guidance; they cause “withdrawal” symptoms, a buzzword for their addictive properties and must be tapered SLOWLY. Seek help from a qualified Medical Psychologist who will work with your primary physician and psychiatrist in developing a treatment plan.
Western Naturopathy
The Western Naturopathic approach calls for identifying nutritional imbalances. Natural products are used to help the body return to normal functioning, rather than trying to trick the body into not reabsorbing serotonin as it was designed to do. Adequate diagnostic testing and close examination of physical as well as psychological symptoms is a hallmark of natural, Functional Medicine. Several natural substances have been shown to help with depression. Significant research has been published supporting effectiveness; sample of some of these studies are referenced below.
Traditional Chinese Medicine
Traditional Chinese Medicine approaches mental or emotional problems such as depression as an imbalance or blockage in one or more of the internal organs (Zang/Fu) and the energy pathways (meridians) that pertain to them. Some common patterns that can manifest as depression are Liver Chi Stagnation, Spleen Chi Deficiency, Kidney Essence Deficiency or Lung and Heart Meridian disorder. The appropriate remedies are chosen by the TCM practitioner based on patterns of symptoms.
Research
Lithium: Lithium has been shown to be effective for management of bipolar mania and depression (9) and is considered first line treatment by the APA (5). “Lithium alone or in combination with an atypical antipsychotic may reduce aggressive behaviors in children and adolescents with CD.” (10) The exact mechanism of action of lithium in psychological and behavioral disorders in humans is “unknown,” however it appears to affect dopamine and serotonin activity. Lithium might increase monoamine oxidase (MAO) activity. It also enhances folate and vitamin B12 transport into brain cells, which might affect mood (11). Reliable evidence demonstrates that a low level of lithium— trace levels found in many water supplies— is effective at reducing suicide rates (7) (12) (13) (14) (15) (16). Low dose lithium has been found to reduce rates of aggression in both humans and animals (7) (17). Lithium appears to work partially by inducing elevations in brain and erythrocyte glycine levels (18).
Although low dose lithium has not been promoted as useful in humans, veterinary science has embraced it for management of healthy animals; lithium is added to commercial pig, chicken and other feed. Low dose lithium has been found helpful for mild cognitive impairment and Alzheimer’s disease (19) (20) (21) (22). Lithium has been used for mania and depression since 1871 (23). It was used as a salt substitute in the 1940’s, although this was abandoned with emergence of dose dependent toxic effects. Lithium carbonate was listed as a controlled substance in 1970.
SAMe: S-Adenosyl methionine is produced naturally in the body and is made from adenosine triphosphate (ATP) and methionine. Several clinical studies show that taking SAMe is more effective than placebo and appears to be as effective as tricyclic antidepressants in trials lasting up to 42 days (26) (27) (28) (29). Rather than harming your liver, SAMe has been shown to combat liver disease as well as arthritis (30). Practice guidelines from the American Psychiatric Association suggest SAMe as a potential alternative to conventional antidepressants for patients with major depression who are interested in using alternative therapies (31).
St. John’s Wort: St. John’s Wort is a yellow-flowering perennial herb indigenous to Europe. It has been extensively studied and is commonly prescribed by psychiatrists in several countries The Cochrane Collaboration has found, “The available evidence suggests that the Hypericum extracts tested in the included trials a) are superior to placebo in patients with major depression; b) are similarly effective as standard antidepressants; and c) have fewer side-effects than standard antidepressants.” (32) St. John’s wort extracts are more effective than placebo for depression (33) (34) (35). Taking St. John’s wort extracts has been shown to improve mood, decrease anxiety and somatic symptoms, and decrease insomnia related to mild to severe major depression (36).
5-HTP: 5-Hydroxytryptophan (5-HTP) is a naturally occurring amino acid and precursor to serotonin and melatonin. It is used for sleep disorders, depression, anxiety, migraine and tension-type headaches, fibromyalgia, binge eating associated with obesity, premenstrual syndrome (PMS), premenstrual dysphoric disorder (PMDD), attention deficit-hyperactive disorder (ADHD), cerebellar ataxia, Ramsey-Hunt syndrome, Down syndrome, insomnia, and as adjunctive therapy in seizure disorder and Parkinson’s disease.
5-HTP readily crosses the blood-brain barrier and increases central nervous system synthesis of serotonin (37). There is good evidence for use for depression (37) (38) including treatment resistant depression (39). Taking 5-HTP orally appears to improve symptoms of primary fibromyalgia syndrome (PFS), including pain severity, morning stiffness, and sleeplessness (40) (41) (42). Preliminary evidence supports the use of 5-HTP for anxiety disorders (43) and cerebellar ataxia (44). Preliminary evidence suggests that taking 5-HTP orally might help reduce appetite, caloric intake, and weight in obese patients (45).
Omega-3 Fatty Acids: Three types of omega-3 fatty acids involved in human physiology are ALA (found in plant oils), EPA, and DHA (both commonly found in marine oils). Common sources of animal omega-3 EPA and DHA fatty acids include fish oils and krill oil. Significant research shows that fish oil can reduce triglyceride levels by 20% to 50% (46). The prescription form, Lovanza, is FDA approved for treating hypertriglyceridemia (47).
The EPA component of omega-3s has been found to be effective at depressive symptoms (48) (49) (50). Some clinical research shows that taking a fish oil supplement orally might reduce the risk of progression from sub-threshold psychosis to full-blown psychotic disorders (51). Taking EPA orally provides modest improvement in aggressive behavior and depression in women with moderately severe borderline personality disorder (52). EPA modestly improves the mental state in patients with schizophrenia compared to placebo (53).
EPA 500 mg orally, three times daily, provides modest, but significant reduction in the frequency of hot flashes compared to placebo (54). Limited evidence supports fish oil use for prevention of restenosis following angioplasy (55). Cochrane found benefit for asthma in children (56). Omega 3’s help with atherosclerosis (57), diabetic neuropathy (58), dysmenorrhea (59), hypertension (60), and rheumatoid arthritis stiffness (61).
Saffron: Saffron is derived from the flower of Crocus sativus, a native of Greece or Southwest Asia. Saffron is used for insomnia, depression, Alzheimer’s disease, fright, shock, asthma, cough, pertussis, and as an expectorant. Women use saffron for menstrual cramps and premenstrual syndrome (PMS). Men use it to prevent (premature ejaculation. Saffron is also used as an aphrodisiac and to induce sweating.
Clinical research shows that taking saffron orally seems to improve symptoms of major depression after 6 weeks of treatment (62) (63). It has shown similar efficacy to fluoxetine 10 mg twice daily in patients with mild-to-moderate depression after 6 weeks of treatment (64) (65).
Some clinical research shows that patients 55 years and older with dementia and probable Alzheimer’s disease treated with saffron orally have comparable cognitive and clinical outcomes to patients receiving conventional therapy with donepezil (Aricept®) 10 mg/day orally after 22 weeks of treatment (66). Saffron significantly improves symptoms of PMS after two menstrual cycles (67).
DHEA: DHEA is endogenously produced in the adrenal glands and in the liver. In men, DHEA is also secreted by the testes. Additionally, the neurons and glial cells in the brain synthesize minute quantities. DHEA and its sulfate ester, dehydroepiandrosterone sulfate (DHEA-S), are interconvertible. DHEA-S is the storage form of DHEA.
Taking DHEA orally might improve symptoms of depression and dysthymia (68) (69) (70). “DHEA treatment may have significant antidepressant effects in some patients with major depression.” (71) “We find DHEA to be an effective treatment for midlife-onset major and minor depression.” (72) “DHEA was superior in the intent-to-treat analysis, where the response rate was 56% (43 of 77) for the DHEA group versus 31% (21 of 68) for the placebo group.” (73)
Taking DHEA orally seems to improve both negative and positive symptoms in patients with schizophrenia (74) (75). Limited evidence indicates DHEA may be effective for erectile dysfunction, lupus (SLE), Addison’s, Chronic fatigue Syndrome and aging skin.
*Statements contained herein have not been evaluated by the Food and Drug Administration. These products are not intended to diagnose, treat and cure or prevent disease. Information provided by CHS is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. Any information given is only intended as a sharing of knowledge and information from scientific world literature. You are encouraged to make your own health care decisions based upon your own research of the subject and in partnership with a qualified health care professional.
Options in Depression Treatment
By David Reinhardt, Ph.D. MSP.Pharm, ABMP
Other substances that need more research
Preliminary evidence suggests several other natural substances offer benefit for depression. Studies are needed to understand if these benefits are due to a direct action on mood or if they are effective because they mitigate nutritional issues. The following substances have preliminary evidence of effectiveness:
Rhodiola (76)
Inositol (77)
Acetyl-L-carnitine (78) (79)
Chromium (80)
L-tryptophan (81)
L-phenylalanine (82)
Phosphatidylserine (83)
Vitamin C (84)
Other Healing Systems
The above discussion examined potentially antidepressant natural substances for a Western Science perspective, as used in Allopathic Medicine and in Western Herbology. Ayurveda and traditional Chinese medicine recognize the symptoms of depression but do not label it as a specific disease for which we must search for a magic pill or elixir.
Ayurveda is an alternative healing system developed over thousands of years and practiced primarily on the Indian subcontinent. From an Ayurvedic perspective, we are at our core healthy, whole, and happy by nature. We should engage in habits and practices that support the emergence of the essential nature and that bring balance to mind, body, and spirit. Ayurvedic medicine may prescribe yoga, breathing, and lifestyle techniques, in addition to using herbal remedies to address imbalance.
Symptoms of depression and anxiety are triggered by excessive mental and physical stress, or disruptions of natural biological rhythms. According to Ayurveda, psychological problems start when fundamental imbalances develop in the biological intelligence that controls all bodily processes. Depression and anxiety can be influenced by many factors, such as diet, digestion, toxin accumulation, stress, exercise levels and daily routine, Ayurveda treatments attempt to balance many physiological functions simultaneously. Ayurvedic formulas for depressive symptoms include 2 substances with limited human research of effectiveness (although several rat studies have been published):
Bacopa monnieri (Brahmi): Brahmi has been shown in many rat studies and a limited number of human studies to help with symptoms of depression (85) (86) (87).
Brahmi has been shown effective for measures of verbal learning, memory, and information processing in healthy men and women (88). It is used for the symptoms of ADHD (89).
Brahmi is available over the counter and costs about $3.12 per month.
Ashwagandha: Ashwagandha is used a part of treatment for arthritis, anxiety, insomnia, tumors, tuberculosis, and chronic liver disease. Ashwagandha is also used as an “adaptogen” to increase resistance to environmental stress. It is also used for improving cognitive function, decreasing inflammation, preventing the effects of aging, for menstrual disorders, fibromyalgia, and asthma. Studies have shown benefit for treating depression, particularly in the elderly (90) (91)
Ashwagandha is available over the counter and costs about $5.25 per month.
Traditional Chinese Medicine (TCM) is a broad range of medicine practices developed over more than 2000 years. TCM’s view of the body places little emphasis on anatomical structures, but is mainly concerned with the identification of functional entities (which regulate digestion, breathing, aging etc.). While health is perceived as harmonious interaction of these entities and the outside world, disease is interpreted as a disharmony in interaction. TCM diagnosis aims to trace symptoms to patterns of an underlying disharmony, by measuring the pulse, inspecting the tongue, skin, and eyes, and looking at the eating and sleeping habits of the person as well as many other things. Plant elements are by far the most commonly, but not solely, used substances; animal, human, and mineral products are also utilized. Complex formulas are tailored to the individual in treatment. Depression, according to TCM, is a disease caused by prolonged stagnation of qi, blood, dampness, or food. The treatment protocol is to break up all stagnation and moisten the internal organs.
Xiao Yao San: Xiao Yao San is a typical TCM depression formula with moderate evidence of effectiveness (92) (93). Xiao Yao San is made up of Bupleurum root (Bupleuri Radix), Chinese peony root (Paeoniae Radix), Chinese Angelica root (Angelicae Radix), White Atractylodes rhizome (Atractylodis Rhizoma), Tuckahoe mushroom (Poria), fresh ginger rhizome (Zingiberis Rhizoma), Chinese licorice root (Glycyrrhizae Radix), and wild mint herb (Menthae Herba). This formula in contraindicated during pregnancy and nursing. It does not contain St. John’s Wort and may be used concurrently with antidepressants or Shine®.
Xiao Yao San is available over the counter and is available from CHS for $20.00 for 100 capsules, a 1 month supply.
Evergreen Shine®: Evergreen makes high quality, modern Chinese formulas based on traditional prinicples and updated using Western standards of research. This formula contains St. John’s Wort, called Guan Ye Lian Qiao in TCM, which has been shown to be effective for depression (see references for St. John’s Wort, above). St. John’s Wort has similar action to Western antidepressants, and inhibits reuptake of serotonin. Because of this Guan Ye Lian Qiao should not be taken concurrently with antidepressant pharmaceuticals. This herb is used in Chinese medicine to clear heat, treat urinary tract and other infections and reduce inflammation. Evergreen Shine® is available from CHS for about $26.00 fper month
Depressive symptoms respond to natural treatments at least as well as pharmaceuticals, and in many cases better. Few if any adverse effects can be expected. They have the advantage of low cost, and freedom from seeing a psychiatrist monthly for monitoring.
Certain facts that are undeniable:
-None of these natural approaches increases depression by 8% (European antidepressant studies) or 4% (American studies, with us being “exceptional,” of course!)
-None of these natural approaches decreases libido
-None of these natural approaches cause serotonin syndrome, Stevens Johnson syndrome or other life threatening effects
-None of these natural approaches require the patient to see a psychiatrist once each month!
-None of these approaches cost $250-800 per month to try.
Although herbal approaches are much safer to try than highly concentrated pharmaceuticals, selection and use should be guided by a healthcare professional that is knowledgeable about interactions and contraindications.
About the author:
Dr. Reinhardt is a Medical Psychologist and head of the Center for Health Science in Long Beach, California. He is on the executive board and a founding member of NAPPP, the National Alliance of Professional Psychology Providers and a Fellow of the Academy of Medical Psychology. Dr. Reinhardt’s special training and passion is in uncovering the roots of poor mental and physical health and finding natural treatments that are both safe and effective. His education includes degrees in Clinical Psychology, Psychopharmacology, Holistic Health, Western Herbology and Engineering. For read more of his work visit his website and blog at CenterforHealthScience.com
References:
(1) www.plosmedicine.org/article/info:doi/10.1371/journal.pmed.0050045
(2) The Journal of the American Medical Association 303 (1): 47–53. doi:10.1001/jama.2009.1943
(3) Arch. Gen. Psychiatry 69 (6): 572–9. doi:10.1001/archgenpsychiatry.2011.2044
(4) Psychiatry Research – 30 April 2014 (Vol. 216, Issue 1, Pages 67-73, DOI: 10.1016/j.psychres.2014.01.042)
(5) American Psychiatric Association Practice Guideline for the Treatment of Patients With Bipolar Disorder, April 2002.
(6) Antidepressants in bipolar disorder: the case for caution. Bipolar Disord. 2003 Dec;5(6):421-33.
(7) Lithium in the public water supply and suicide mortality in Texas. J Psychiatr Res. 2013 Mar;47(3):407-11. doi: 10.1016/j.jpsychires.2012.12.002. Epub 2013 Jan 9.
(8) epocrates.com/ drug monograph Id=4012
(9) McKevoy GK, ed. AHFS Drug Information. Bethesda, MD: American Society of Health-System Pharmacists, 1998.
(10) CNS Drugs. 2009;23(1):59-69. doi: 10.2165/0023210-200923010-00004.
(11) Schrauzer GN. Lithium: occurrence, dietary intakes, nutritional essentiality. J Am Coll Nutr 2002;21:14-21.
(12) BMJ. 2013 Jun 27;346:f3646. doi: 10.1136/bmj.f3646.
(13) The British Journal of Psychiatry (2011) 198: 346-350
(14) Schrauzer GN, Shrestha KP: Lithium in drinking water and the
incidences of crimes, suicides, and arrests related to drug
addictions. Biol. Trace Elem. Res. 25(2): 105-13, 1990.
(15) Fierro AA: Natural low dose lithium supplementation in manicdepressive
disease. Nutr. Perspectives January, 1988:10-11.
(16) Lithium in drinking water
and suicide rates across the East of England. Br J Psychiatry 2011,
198:406–407.
(17) Journal of Veterinary Pharmacology and Therapeutics Volume 2, Issue 4, pages 299–303, December 1979
(18) Nunes MA, Viel TA, Buck HS. Microdose lithium treatment stabilized cognitive impairment in patients with Alzheimer’s disease. Curr Alzheimer Res (2013) 10(1):104-107.
(19) Neuropsychobiology 1983;9:215–218 (DOI:10.1159/000117967)
(20) Forlenza OV, Diniz BS, Radanovic M, et al. Disease-modifying properties of long-term lithium treatment for amnestic mild cognitive impairment: randomised controlled trial. Br J Psychiatry (2011) 198(5):351-356.
(21) Straten G, Saur R, Laske C, et al. Influence of lithium treatment on GDNF serum and CSF concentrations in patients with early Alzheimer’s disease.? Curr Alzheimer Res (2011) 8(8):853-859.
(22) Leyhe T, Eschweiler GW, Stransky E, et al. Increase of BDNF serum concentration in lithium treated patients with early Alzheimer’s disease. J Alzheimers Dis (2009) 16(3):649-656
(23) Robert Howland, the history of Lithium. //www.psycheducation.org/depression/meds/LithiumHistory.htm
(24) JAMA. 1949;139(11):685-688. doi:10.1001/jama.1949.02900280001001.
(25) Janicak PG, Lipinski J, Davis JM, et al. S-adenosylmethionine in depression. A literature review and preliminary report. Ala J Med Sci 1988;25:306-13.
(26) De Vanna M, Rigamonti R. Oral S-adenosyl-L-methionine in depression. Curr Ther Res 1992;52:478-85.
(27) Gaster B. S-adenosylmethionine (SAMe) for treatment of depression. Alternative Medicine Alert, 1999;12:133-5
(28) Bressa GM. S-adenosyl-l-methionine (SAMe) as antidepressant: meta-analysis of clinical studies. Acta Neurol Scand Suppl 1994;154:7-14
(29) Kagan BL, Sultzer DL, Rosenlicht N, Gerner RH. Oral S-adenosylmethionine in depression: a randomized, double-blind, placebo-controlled trial. Am J Psychiatry 1990;147:591-5.
(30) ?S-Adenosyl-L-Methionine for Treatment of Depression, Osteoarthritis, and Liver Disease? (Report). Agency for Healthcare Research and Quality. Retrieved 2012-08-31.
(31) Work Group for Major Depressive Disorder. Practice Guideline for the Treatment of Patients With Major Depressive Disorder, Third Edition. American Psychiatric Association, May 2010 (Published October 2010).
(32) Cochrane Database Syst Rev. 2005;(2):CD000448.
(33) Anon. A better treatment for depression? UC Berkeley Wellness Letter 1997;13:1-2.
(34) olz HP. Controlled clinical trials of hypericum extracts in depressed patients – an overview. Pharmacopsychiatry 1997;30 Suppl 2:72-6
(35) Chatterjee SS, Noldner M, Koch E, Erdelmeier C. Antidepressant activity of hypericum perforatum and hyperforin: the neglected possibility. Pharmacopsych 1998;31:7-1
(36) Gaster B, Holroyd J. St John’s wort for depression. Arch Intern Med 2000;160:152-6
(37) Shaw K, Turner J, Del Mar C. Tryptophan and 5-hydroxytryptophan for depression. Cochrane Database Syst Rev 2002;(1):CD003198
(38) Nakajima T, Kudo Y, Kaneko Z. Clinical evaluation of 5-hydroxy-L-tryptophan as an antidepressant drug. Folia Psychiatr Neurol Jpn 1978;32:223-30
(39) Coppen A, Whybrow PC, Noguera R, et al. The comparative antidepressant value of L-tryptophan and imipramine with and without attempted potentiation by liothyronine. Arch Gen Psychiatr 1972;26:234-41
(40) Sarzi Puttini P, Caruso I. Primary fibromyalgia syndrome and 5-hydroxy-L-tryptophan: a 90-day open study. J Int Med Res 1992;20:182-9
(41) Nicolodi M, Sicuteri F. Fibromyalgia and migraine, two faces of the same mechanism. Serotonin as the common clue for pathogenesis and therapy. Adv Exp Med Biol 1996;398:373-9
(42) Caruso I, Sarzi Puttini P, Cazzola M, Azzolini V. Double-blind study of 5-hydroxytryptophan versus placebo in the treatment of primary fibromyalgia syndrome. J Int Med Res 1990;18:201-9
(43) Kahn RS, Westenberg HG. L-5-hydroxytryptophan in the treatment of anxiety disorders. J Affect Disord 1985;8:197-200
(44) Trouillas P, Brudon F, Adeleine P. Improvement of cerebellar ataxia with levorotatory form of 5-hydroxytryptophan: a double-blind study with quantified data processing. Arch Neurol 1988;45:1217-22;
(45) Cangiano C, Ceci F, Cancino A, et al. Eating behavior and adherence to dietary prescriptions in obese adult subjects treated with 5-hydroxytryptophan. Am J Clin Nutr 1992;56:863-7
(46) Eritsland J, Arnesen H, Seljeflot I, Hostmark AT. Long-term metabolic effects of n-3 polyunsaturated fatty acids in patients with coronary artery disease. Am J Clin Nutr 1995;61:831-6
(47) Reliant Pharmaceuticals. Omacor package insert. Liberty Corner, NJ; December, 2004
(48) Nemets B, Stahl Z, Belmaker RH. Addition of omega-3 fatty acid to maintenance medication treatment for recurrent unipolar depressive disorder. Am J Psychiatry 2002;159:477-9
(49) Peet M, Horrobin DF. A dose-ranging study of the effects of ethyl-eicosapentaenoate in patients with ongoing depression despite apparently adequate treatment with standard drugs. Arch Gen Psychiatry 2002;59:913-9
(50) Omega-3 fatty acids in depression: a review of three studies. CNS Neurosci Ther. 2009 Summer;15(2):128-33.
(51) Amminger GP, Schafer MR, Papageorgiou K, et al. Long-chain omega-3 fatty acids for indicated prevention of psychotic disorders: a randomized, placebo-controlled trial. Arch Gen Psychiatry 2010;67:146-54
(52) Zanarini MC, Frankenburg FR. Omega-3 Fatty acid treatment of women with borderline personality disorder: a double-blind, placebo-controlled pilot study. Am J Psychiatry 2003;160:167-9
(53) Joy CB, Mumby-Croft R, Joy LA. Polyunsaturated fatty acid supplementation for schizophrenia. Cochrane Database Syst Rev 2006;3:CD001257
(54) Lucas M, Asselin G, Merette C, et al. Effects of ethyl-eicosapentaenoic acid omega-3 fatty acid supplementation on hot flashes and quality of life among middle-aged women: a double-blind, placebo-controlled, randomized clinical trial. Menopause 2009;16:357-66
(55) Maresta A, Balduccelli M, Varani E, et al. Prevention of postcoronary angioplasty restenosis by omega-3 fatty acids: main results of the Esapent for Prevention of Restenosis Italian Study (ESPRIT). Am Heart J 143:E5
(56) Woods RK, Thien FC, Abramson MJ. Dietary marine fatty acids (fish oil) for asthma in adults and children. Cochrane Database Syst Rev 2002;(2):CD001283
(57) Sacks FM, Stone PH, Gibson CM, et al. Controlled trial of fish oil for regression of human coronary atherosclerosis. HARP Res Group. J Am Coll Cardiol 1995;25:1492-8
(58) Shimizu H, Ohtani K, Tanaka Y, et al. Long-term effect of eicosapentaenoic acid ethyl (EPA-E) on albuminuria of non-insulin dependent diabetic patients. Diabetes Res Clin Pract 1995;28:35-40
(59) Deutch B, Jorgensen EB, Hansen JC. Menstrual discomfort in Danish women reduced by dietary supplements of omega-3 PUFA and B12 (fish oil or seal oil capsules). Nutr Res 2000;20:621-31
(60) Prisco D, Paniccia R, Bandinelli B, et al. Effect of medium-term supplementation with a moderate dose of n-3 polyunsaturated fatty acids on blood pressure in mild hypertensive patients. Thromb Res 1998;1:105-12
(61) van der Tempel H, Tulleken JE, Limburg PC, et al. Effects of fish oil supplementation in rheumatoid arthritis. Ann Rheum Dis 1990;49:76-80
(62) Akhondzadeh S, Fallah-Pour H, Afkham K, et al. Comparison of Crocus sativus L. and imipramine in the treatment of mild to moderate depression: A pilot double-blind randomized trial [ISRCTN45683816]. BMC Complement Altern Med 2004;4:12
(63) Akhondzadeh S, Tahmacebi-Pour N, Noorbala AA, et al. Crocus sativus L. in the treatment of mild to moderate depression: a double-blind, randomized and placebo-controlled trial. Phytother Res 2005;19:148-51
(64) Noorbala AA, Akhondzadeh S, Tahmacebi-Pour N, Jamshidi AH. Hydro-alcoholic extract of Crocus sativus L. versus fluoxetine in the treatment of mild to moderate depression: a double-blind, randomized pilot trial. J Ethnopharmacol 2005;97:281-4.
(65) Akhondzadeh Basti A, Moshiri E, Noorbala AA, et al. Comparison of petal of Crocus sativus L. and fluoxetine in the treatment of depressed outpatients: a pilot double-blind randomized trial. Prog Neuropsychopharmacol Biol Psychiatry 2007;31:439-42
(66) Akhondzadeh S, Sabet MS, Harirchian MH, et al. A 22-week, multicenter, randomized, double-blind controlled trial of Crocus sativus in the treatment of mild-to-moderate Alzheimer’s disease. Psychopharmacology 2010;207:637-43.
(67) Agha-Hosseini M, Kashani L, Aleyaseen A, et al. Crocus sativus L. (saffron) in the treatment of premenstrual syndrome: a double-blind, randomised and placebo-controlled trial. BJOG 2008;115:515-9
(68) Wolkowitz OM, Reus VI, Keebler A, et al. Double-blind treatment of major depression with dehydroepiandrosterone. Am J Psychiatry 1999;156:646-9
(69) Bloch M, Schmidt PJ, Danaceau MA, et al. Dehydroepiandrosterone treatment of midlife dysthymia. Biol Psychiatry 1999;45:1533-41
(70) Wolkowitz OM, Reus VI, Manfredi F, et al. Dehydroepiandrosterone (DHEA) treatment of depression. [Abstract] Biol Psychiatry 1997;41:311-8
(71) Double-blind treatment of major depression with dehydroepiandrosterone. Am J Psychiatry. 1999 Apr;156(4):646-9.
(72) Dehydroepiandrosterone monotherapy in midlife-onset major and minor depression. Arch Gen Psychiatry. 2005 Feb;62(2):154-62.
(73) Placebo-controlled trial of dehydroepiandrosterone (DHEA) for treatment of nonmajor depression in patients with HIV/AIDS. Am J Psychiatry. 2006 Jan;163(1):59-66.
(74) Strous RD, Maayan R, Lapidus R, et al. Dehydroepiandrosterone augmentation in the management of negative, depressive, and anxiety symptoms in schizophrenia. Arch Gen Psychiatry 2003;60:133-41
(75) The clinical and therapeutic potentials of dehydroepiandrosterone and pregnenolone in schizophrenia. Ritsner MS. Neuroscience. 2011 Sep 15;191:91-100.
(76) Darbinyan G, Aslanyan G, Amroyan E. Clinical trial of Rhodiola rosea L. extract SHR-5 in the treatment of mild to moderate depression. Nord J Psychiatry 2007;61:343-8
(77) Mukai T, Kishi T, Matsuda Y, Iwata N.A meta-analysis of inositol for depression and anxiety disorders. Hum Psychopharmacol. 2014 Jan;29(1):55-63.
(78) Bella R, Biondi R, Raffaele R, Pennisi G. Effect of acetyl-L-carnitine on geriatric patients suffering from dysthymic disorders. Int J Clin Pharmacol Res 1990;10:355-60
(79) Tempesta E, Casella L, Pirrongelli C, et al. L-acetylcarnitine in depressed elderly subjects. A cross-over study vs placebo. Drugs Exp Clin Res 1987;13:417-23
(80) Davidson JR, Abraham K, Connor KM, McLeod MN. Effectiveness of chromium in atypical depression: a placebo-controlled trial. Biol Psychiatry 2003;53:261-4
(81) Walinder J, Skott A, Carlsson A, et al. Potentiation of the antidepressant action of clomipramine by tryptophan. Arch Gen Psychiatry 1976;33:1384-89
(82) Beckmann H, Athen D, Olteanu M, Zimmer R. DL-phenylalanine versus imipramine: a double-blind controlled study. Arch Psychiatr Nervenkr 1979;227:49-58
(83) Maggioni M, Picotti GB, Bondiolotti GP, et al. Effects of phosphatidylserine therapy in geriatric patients with depressive disorders. Acta Psychiatr Scand 1990;81:265-70
(84) Efficacy of supplementary vitamins C and E on anxiety, depression and stress in type 2 diabetic patients: a randomized, single-blind, placebo-controlled trial. Mazloom Z, Ekramzadeh M, Hejazi N. Pak J Biol Sci. 2013 Nov 15;16(22):1597-600.
(85) Effects of a Standardized Bacopa monnieri Extract on Cognitive Performance, Anxiety, and Depression in the Elderly: A Randomized, Double-Blind, Placebo-Controlled Trial. The Journal of Alternative and Complementary Medicine. July 2008, 14(6): 707-713.
(86) A Clinical Study on Effect of Brahmi Ghrita on Depression. AYU. 2008: 29: 4: 207-214
(87) Comparative Evaluation of the efficacy and side effects of imipramine, sertraline and an ayurvedic formulation in patients of depression. J Bhargava, ZY Khan – Journal of Clinical and Diagnostic Research, 2012 – jcdr.net
(88) Stough C, Lloyd J, Clarke J, et al. The chronic effects of an extract of Bacopa monniera (Brahmi) on cognitive function in healthy human subjects. Psychopharmacology 2001;156:481-4
(89) Randomized controlled trial of standardized Bacopa monniera extract in age-associated memory impairment. Indian Journal of Psychiatry 2006 Oct-Dec 48(4): 238-242.
(90) Impact of Ashwagandha on the mental health profile of Elderly Women.
K Chauhan, G Patil – European Scientific Journal, 2013 – eujournal.org
(91) Anxiolytic-antidepressant activity of Withania somnifera glycowithanolides: an experimental study. Phytomedicine. 2000 Dec;7(6):463-9.
(92) Chinese herbal formula xiao yao san for treatment of depression: a systematic review of randomized controlled trials. Evid Based Complement Alternat Med. 2012;2012:931636. doi: 10.1155/2012/931636. Epub 2011 Aug 22.
(93) Chinese herbal formula Xiao Yao San for treatment of depression: a systematic review of randomized controlled trials. Zhang Y, et al.: Evid Based Complement Alternat Med. 2012;2012:931636.
© 2014 CenterforHealthScience.com This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Statements contained herein have not been evaluated by the Food and Drug Administration. These products are not intended to diagnose, treat and cure or prevent disease. Information provided by CHS is not intended to replace a one-on-one relationship with a qualified health care professional and is not intended as medical advice. Any information given is only intended as a sharing of knowledge and information from scientific world literature. You are encouraged to make your own health care decisions based upon your own research of the subject and in partnership with a qualified health care professional.