Lithium Orotate: The Unique Safe Mineral with Multiple Uses
by Ward Dean, M.D. and Jim English
Reprinted by permission from Pat Whittington of Vitamin Research News
Lithium is a mineral with a cloudy reputation. It is an alkali metal in the same family as sodium, potassium and other elements. Although lithium is highly effective for supporting those who experience depression or foul moods, its pharmaceutical (prescription) versions, lithium carbonate and lithium citrate, must be used with caution. The reason for the caution with prescription lithium is because lithium in these forms is poorly absorbed by the cells of the body — and it is within the cells that lithiums' therapeutic effects take place. Lithium ions are believed to act only at particular sites on the membranes of intracellular structures like mitochondria and lysosomes.
Consequently, because of this poor intracellular transport, high dosages of pharmaceutical forms of lithium must be taken in order to obtain a satisfactory therapeutic effect. Unfortunately, these therapeutic dosages cause blood levels to be so high that they border on toxic levels. Consequently, patients taking prescription lithium must be closely monitored for toxic blood levels. Serum lithium and serum creatinine levels of prescription lithium-treated patients should be monitored every 3-6 months.
Toxicity effects of lithium may include hand tremors, frequent urination, thirst, nausea, and vomiting. Even higher doses may cause drowsiness, muscular weakness, poor coordination, ringing in the ears, blurred vision, and other symptoms.
There has been concern that long-term lithium treatment may damage kidney function, but data in this regard are equivocal. Renal insufficiency without a known cause has occurred in the general population, and the incidence of renal failure among manic-depressive patients not treated with lithium remains unknown.
Most patients treated with lithium are also taking other medications and it is just as likely that the few known cases of renal failure in patients taking lithium were due to other medications that they were simultaneously taking.2-5
Nevertheless, with potential side effects like this, why in the world would anyone want to take lithium? It is because lithium has been found to be one of the most effective support medications for those who experience "the blues."
Mood disorders are characterized by mood swings that usually cycle back and forth between up cycles and down cycles. The down phase is characterized by sluggishness (inertia), loss of self-esteem, helplessness, withdrawal and sadness, with suicide being a risk. The up (or manic) phase is characterized by elation, hyperactivity, over-involvement in activities, inflated self-esteem, a tendency to be easily distracted, and little need for sleep. In either phase there is frequently a dependence on alcohol or other substances of abuse. The disorder first appears between the ages of 15 and 25 and affects men and women equally. The cause is unknown, but hereditary and psychological factors may play a role. The incidence is higher in relatives of people with the disorders. A psychiatric history of mood swings, and an observation of current behavior and mood are important in the diagnosis of this disorder.7
Hospitalization may be required during an acute phase to control the symptoms. Antidepressant drugs may be given; anticonvulsants (Carbamazepine, Valproic acid, Depakote) may also be used. (These substances deplete body stores of L-carnitine and Taurine. Supplementation with several grams daily of these supplements greatly ameliorates adverse side effects of these drugs).
Lithium, however, is the treatment of choice for "the blues," serving as a consistent mood enhancer in 70-80 percent of people.
Mortality-lowering, Anti-Suicidal Effect of Lithium
The mortality of people with "ups and downs" is markedly higher than that of the general population. The increased mortality is mainly, but not exclusively, caused by suicide. Studies have shown that the mortality of these patients given long-term lithium treatment is markedly lower than that of patients not receiving lithium. The frequency of suicidal acts among treated patients is significantly lower than patients given other antidepressants or carbamazepine. The results of mortality studies are consistent with the assumption that lithium-treatment protects against suicidal behavior. 8-13
Recurrent Major Affective Disorder
In addition to its well-recognized benefits in the management of "mental ups and downs," trials have conclusively demonstrated that lithium is also an effective treatment for recurrent major affective disorder.14-16 Although physicians in Europe have successfully used lithium for this indication for many years, American psychiatrists do not share their appreciation of lithium's safety and effectiveness for conditions. Perhaps it is due to a difference in the lithium preparations they have at their disposal.
Superiority of Lithium Orotate
The lithium salt of orotic acid (lithium orotate) improves the specific effects of lithium many-fold by increasing lithium bio-utilization. The orotates transport the lithium to the membranes of mitochondria, lysosomes and the glia cells. Lithium orotate stabilizes the lysosomal membranes and prevents the enzyme reactions that are responsible for the sodium depletion and dehydration effects of other lithium salts. Because of the superior bioavailability of lithium orotate, the therapeutic dosage is much less than prescription forms of lithium. For example, in cases of severe mental maladjustment, the therapeutic dosage of lithium orotate is 150 mg/day. This is compared to 900-1800 mg of the prescription forms (carbonate). In this dosage range of lithium orotate, there are no adverse lithium side effects and no need for monitoring blood serum measurements.17
Other Uses for Lithium Orotate
Lithium orotate has also been used with success in supporting those with migraine and cluster headaches, low white blood cell counts, juvenile convulsive disease, alcoholism and liver disorders.18 Nieper also reports that patients with myopia (nearsightedness) and glaucoma often benefit from the slight dehydrating effect of lithium on the eye, resulting in improvement in vision and reduction of intraocular pressure.17
|Serving Size: 1 Capsule|
|Amount Per Serving
||% Daily Value|
|Lithium Orotate (providing 4.8 mg elemental lithium)
|*Daily Value not established
|Other Ingredients: Microcrystalline cellulose and Hydroxypropyl methylcellulose (Vcap). Contains no added starch, salt, wheat, gluten, corn, coloring, or dairy products.|
Restrictions for Lithium Orotate: Canada - No import. Japan - 1 bottle per order
Dosage and Use:
- For general mood enhancement and mental acuity, suggested dose is 1 capsule of lithium orotate twice per day with meals as a part of your overall/everyday life enhancement protocol.
- Most effectively utilized when taken with meals.
- In cases of more severe mental maladjustment and/or for those who want to reduce their amount of alcohol consumption, the therapeutic dosage of lithium orotate is 150 (elemental) mg/day (30 caps/day). Once a level of control has been established, lowering the dose gradually over time is suggested.
References (this article only):
1. Aronson JK, Reynolds DJM. ABC of monitoring drag therapy: lithium. BMJ. 1992;305: 1273-1276.
2. Schou M, Effects of long-term lithium treatment on kidney function: an overview. J Psychiat Res, 1988;22.,287-296.
3. Waller DG, Edwards TG. Lithium and the kidney: an update. Psycliol Mod. 1989; 19:825-83 1.
4. Gitlin MJ. Lithium-induced renal insufficiency., J Clin Psychopharmacol. 1993) 13:276-279.
5, Kallner G,.Petterson IJ. Renal, thyroid and parathyroid function during lithium treatment: laboratory test in 207 people treated for 1-30 years. Acta Psychiatr Scand. 1995;91:48-5 1.
6. Baastrup PC, Schou M. Lithium as a prophylactic agent: its effects. Arch Gen Psychiatry. 1967; 16:162-172.
7. Goodwin FK, Jamison KR. Manic-Depressive Illness. Oxford, England: Oxford University Press; 1990.
8. Mueller-Oerlinghausen D, Ahrens B, Volk J, Grof P, Grof E, Schou M, Vestergaard P, Lenz G, Sinihandl C, Tlau K, Wolf R. Reduced mortality of patients in long-term lithium treatment, an international collaborative study by IGSLI. Psychiatry Res. 1991;36:329-331.
9. Ahrens B, Mueller-Oerlinghausen 3, Schou M, Wolf T, Alda M, Grof. E. Grof P, Lejiz G, Simhandl C, Thau K, Vestergaard P, Wolf R, Moeller H. Cardiovascular and suicide mortality of affective disorders may be reduced by lithium prophylaxis. J Affect DI-Y, 1995;33:67-75.
10. Mueller-Oerlinghausen B, Mueser-Causemam B, Volk J. Suicides and parasuicides in a high-risk patient group on and off lithium long-term medication, J Affect Dis. 1992;25: 261-270.
11. Felber- NV, Kyber A. Suizide und Parasuizide wachrend und aubetadserhalb einer Lithiumprophylaxe. In-, Muclicr-Oerlinghausen B, Berghoefer A, eds. Ziele und Ergebnisse der medikagivitoeseyi I-i-opiiylaice affektiver Psychoseii. Stuttgart, Germany, Thieme; 1994:53-59.
12. Thies-Flechtner K, Seibert W, Walther A, Greil W, Mueller-Oerlinghausen B, Suizide bei rezldlvprophylaktisch behandelten Patienten mit affektiven Psychosen. In: Mueller-Oerlinghausen B, Berghoefer A, eds. Ziele und Ergebnisse der medikamentoesen Prophylaxe offekliver Psychosen. Stuttgart, Germany. Thieme; 1994,61-64.
13. Schou M.. Mortality-lowering effect of prophylactic lithium treatment, a look at the evidence, Pharmacopsychiatry. 1995;28: 1.
14. Souza FGM, Goodwin GM. Lithium treatment and prophylaxis in unipolar: a meta-analysis, Br J Psychiatry. 1991; 158:666-675.
15. Johnstone EC, Owens DGC, Lambert MT, Crow TJ, Frith CD, Done DJ. Combination tricyclic and lithium maintenance medication in unipolar and bipolar. J Affect Dis, 1990;20:225-233.
16. Prien RF, Kupfer DJ, Mansky PA, Small JG, Iuason VB, Voss CB, Johnson WE. Drug therapy in the prevention of recurrences in unipolar and bipolar. Arch Gen Psychiatry, 1984;41.1096-1104.
17. Nieper HA The clinical application of lithium orotate. Agressologie 14(6). 407-411, 1973.
18. Sartori HE, Lithium orotate in the treatment of alcoholism and related conditions, Alcohol 1986 Mar; 3 (2): 97-100.
19. Nieper HA The effect of a combination of Calcium-orotate and Lithium orotate on primary and secondary chronic hepatitis and primary and secondary liver cirrhosis. From lecture Intl Acad of Prevent Med, Washington, DC March 9, 1974.