Glucosamine Benefits and Osteoarthritis Treatment

Glucosamine plays an substantial role in building cartilage. It is an critical component in the body’s ability to make GAGs (glycosaminoglycans) and proteoglycans which are compounds of cartilage. They, are the core materials used by the body to make cartilage, synovial fluid and other elements of the skeletal system. As a person ages, the amount of glycosaminoglycans decreases leaving tissues and joints susceptible to pain and injury. Taking glucosamine supplements (glucosamine in most supplements is derived from shellfish) can increase the body’s production of proteoglycans and glycosaminoglycans significantly and improve the natural repair process.

Glucosamine Benefits and Arthritis Treatment

Glucosamine sulphate is often used to reduce pain and swelling in people suffering from osteoarthritis, the most widespread form of arthritis. It is also used to treat symptoms of TMJ (temporomandibular joint) arthritis in the jaw. Several studies demonstrate that glucosamine may be an effective therapy for osteoarthritis. These studies suggest that glucosamine; 1-Reduces osteoarthritis pain, 2-Improves function in patients with hip or knee osteoarthritis, 3-Reduces joint swelling and stiffness, 4-Provides relaxation from osteoarthritis symptoms for up to three months after therapy is stopped. As a supplement, glucosamine sulfate provides the raw material needed by the body to manufacture a mucopolysaccharide found in cartilage. There are different forms of glucosamine including glucosamine sulfate, glucosamine hydrochloride (HCL), and N-acetylglucosamine (GlcNAc). Glucosamine sulfate is the most researched form of glucosamine. Glucosamine may be administered via intramuscular, intravenous, or oral routes.

GlucosamineIn osteoarthritis, there is a progressive degeneration of cartilage GAG (glycosaminoglycans). Glucosamine is a important structural component within joint tissue and is the starting point of the synthesis of several major macromolecules including glycoproteins, glycolipids and glycosaminoglycans. Glucosamine facilitates the synthesis of glycosaminoglycans (GAGs), and therefore replenishing the availability of these molecules would slow the degeneration of cartilage. According to a study reported in the Jan, 2001 edition of the Lancet, glucosamine helps control osteoarthritis.

In a study, which included 318 patients, glucosamine sulphate had a important benefit over a placebo and an even stronger effect than paracetamol in improving both pain and function. A 3-year study of 212 participants found indications that glucosamine may protect joints from further damage. Over the course of the study, patients given glucosamine demonstrated some improvements in pain and mobility, Also, x-rays showed that glucosamine therapy prevented progressive damage to the knee joint. At the end of the study, participants taking glucosamine had no joint-space narrowing, whereas participants taking placebo had an average joint-space loss of 0.31 mm after 3 years.

In another clinical trial, 60 patients with primary osteoarthritis in either one or both knees were randomised to receive a 1500 mg sachet of glucosamine or a placebo. After twelve weeks, there were no improvements in the placebo group but those who received glucosamine sulphate reported important improvements in resting and moving pain, overall pain, stiffness and function. A study reported in the Archives of Internal Medicine evaluated osteoarthritis patients over 3 years during which 202 participants were given glucosamine while others were given a placebo. Glucosamine sulfate slowed the progress of knee arthritis, and the participants taking glucosamine reported a diminution in pain as well as stiffness compared with the placebo group. Participants taking glucosamine had no joint-space narrowing, while participants taking placebo had a joint-space narrowing of 0.19 mm.

Glucosamine sulfate is a safe alternative to NSAID pain relievers, such as ibuprofen and aspirin. A 1994 study in Osteoarthritis and Cartilage showed that glucosamine was as powerful as ibuprofen drug for controlling the symptoms of osteoarthritis. In a study involving 178 patients with osteoarthritis of the knee, those taking glucosamine sulphate 1500 mg daily for 4 weeks demonstrated improvements similar to those seen with ibuprofen 1200 mg daily. The important advantage of taking glucosamine sulfate is that it does not have any of the adverse effects commonly associated with NSAIDs such as Ibuprofen or Aspirin, or COX-2 such as Celebrex, the medications that have been used for the therapy of arthritis.

The medical journal Clinical Drug Investigation findings one study found MSM (methylsulfonylmethane), when used along with glucosamine sulfate, was effective for reducing inflammation and pain associated with osteoarthritis of the knee. New studies have shown that the combination of chondroitin and glucosamine may be effective in reducing moderate to severe knee pain from osteoarthritis. Like glucosamine sulfate, chondroitin helps produce substances necessary for the formation of connective tissue. Also, chondroitin may have the ability to protect existing cartilage from prematurely breaking down by inhibiting cartilage-destroying enzymes. The combined use is known to produce a synergistic effect. One study reported in the February, 2006, edition of the “New England Journal of Medicine” concluded glucosamine taken with chondroitin sulfate, benefited those with moderate-to-severe osteoarthritis pain.

The most common kind of arthritis, called osteoarthritis, causes degeneration of cartilage and bone at the joints and can occur at the TMJ (temporomandibular joint) arthritis. Some researches shows that taking glucosamine sulfate works about as well as the NSAID ibuprofen for relieving jaw pain. The Journal of Rheumatology reported a study which concluded glucosamine and ibuprofen reduce pain levels in patients with TMJ degenerative joint disease. Other study has concluded a reduction in pain associated with combination treatment of chondroitin sulfate (1200mg) and glucosamine hydrochloride (1500mg) for a period of twelve weeks.

Dosage

For osteoarthritis, the standard adult dose of glucosamine used in most studies was 500 mg of glucosamine sulfate taken three times a day. 1,500 milligrams dose taken once daily is another option. Some publications use 20 mg for each kilogram of body weight per day. Glucosamine is also available as an injectable form that your physician can insert directly into a joint.

Side Effects

Glucosamine may cause mild stomach upset, nausea, heartburn, constipation and diarrhea. Since glucosamine can be made from the shells of crab, shrimp, and other shellfish, individuals with shellfish allergy may have an allergic reaction to glucosamine products. Glucosamine may increase the risk of bleeding, especially if you also take blood thinners like aspirin, clopidogrel or warfarin. Glucosamine may affect your insulin or other blood-sugar-lowering drug. Some studies have shown that when taken in pill form, glucosamine has no effect on insulin, however, when taken by injection, glucosamine may cause insulin resistance.

Stinging Nettle BPH Treatment and Researches

Stinging Nettle are from the plant family of Urticaceae. Urtica urens and Urtica dioica are botanically very similar and are usually distributed together in the wild. Especially useful for men, nettle root plays a key role in promoting a healthful prostate and urinary tract function. Nettle root is used widely in Europe to treat BPH (Benign Prostatic Hyperplasia).

Stinging Nettle and Prostate Health

Nettle root has 5-alpha reductase enzyme blocking properties and is thus beneficial for conditions associated with an enlarged prostate, such as frequent or difficult urination. This enzyme converts testosterone into dihydrotestosterone, a strong androgen hormone associated with prostate enlargement, low testosterone levels in older men. Nettle root has been shown to inhibit the binding of sex hormone-binding globulin (SHBG) to the prostate cell membrane. Several researches have showed a combination of nettle root,  pygeum, saw palmetto, and pumpkin seed may be effective as an BPH therapy and in reducing post urination dripping, improving urinary flow, emptying the bladder completely, and decreasing frequent nighttime urination.

Lab experiments have shown stinging nettle to be comparable to finasteride (Proscar®) in slowing the growth of certain prostate cells. The polysaccharide fraction, of the 20 percent methanolic extract of nettle roots, was able to decrease the induced growth of prostate gland by 33 % in mice. Germany Universitätsklinik Essen formally investigated the efficacy of nettle root extract and found the antiphlogistic and antiproliferative properties of the nettle extract to provide a safe treatment option for enlarged prostate.

Since 1995, three clinical trials of a nettle/saw palmetto combination have been reported in German medical journals. The studies used two capsules per day of 120 mg nettle root extract and 160 mg saw palmetto extract. The Journal of Herbal Pharmacotherapy, 2005 published a study investigating nettle (Urtica dioica)  for the therapy of BPH. It has been found that patients with BPH that underwent nettle therapy for six months showed  an improved urinary flow rate, lower postvoid residual urine volume and smaller prostate gland size.

In a study in Poland 134 people with symptoms of BPH were assigned to receive 2 capsules of the standard dose of an nettle (300 mg) and pygeum africanum bark extract (25 mg) or two capsules containing half the standard dose, twice daily for 8 weeks. After 28 days of therapy, urine flow, residual urine, and nycturia were significantly decreased in both treatment groups. After 56 days of therapy, further significantly decreased in both treatment groups. Clinical studies held in the University Clinics of Cologne in Germany, for people suffering from LUTS (Lower Urinary Tract Symptoms), caused by BHP proved to have a higher success rate of 34% for those taking the roots of nettle (Urtica dioica) compared with the patients who took Tamsulosin drug.

Stinging Nettle to Help Arthritis Pain

Stinging nettle has been used for hundreds of years to treat painful muscles and joints and arthritis. Researches have shown that the extract of the nettle leaf suppresses cytokines associated with inflammatory joint illness.

Stinging Nettle Benefits For Arthritis

In several studies nettle extracts were documented with anti-inflammatory effects as well as to be helpful at relieving arthritis pain and inflammation in humans. Studies conducted in Germany have showed scientifically that nettle is capable of inhibiting the genetic transcription factor that activates TNF-a and IL-1B. An ethanolic extract was found to suppress HLE (human leukocyte elastase). Human leukocyte elastase is one of the most destructive enzymes released by polymorphonuclear granulocytes, which migrate into tissues during the inflammatory process. Nettle extract in capsule form is prescribed in Germany for the pain of rheumatoid arthritis and osteoarthritis. Two clinical studies (Chubasik et al 1997) produced promising results of improvement in pain at rest (55%), pain on exercise (45%), physical impairment (38%) and reduction in consumption of non-steroidal anti-inflammatories in 60% of patients.

In a study reported in the Journal of the Royal Society of Medicine in June 2000 issue that nettle leaf can decrease osteoarthritic pain in the base of the thumb when applied to the painful area. Using nettles may decrease the need for NSAID (Nonsteroidal Antiinflammatory Drug). In a clinical trial of 37 people with acute arthritis, 50 g of stewed nettle leaf consumed on a daily combined with 50 mg of diclofenac was shown to be as effective as the full 200 mg dose of diclofenac in the therapy of symptoms, over a two week period. In a study reported in the Dec 2009 issue of “Arthritis Research and Therapy“, found that a combination of nettles, fish oil and vitamin E reduction the need for analgesics and other drugs to decrease the symptoms of osteoarthritis.

The tiny stingers of the nettle plant provide microinjections of several chemicals responsible for the stinging sensation the plant causes. The needles pump a mixture of formic acid, histamine, serotonin (5-hydroxytryptamine), acetylcholine, moroidin and leukotrienes into the epidermis, producing a stinging or burning sensation. These chemicals are anti-inflammatory and pain reducing. These neuro-transmitters send and receive signals to the brain and act on nerve endings to block the transmission and perception of pain. The benefits of nettle as a possible local painkiller were studied in 27 participants with osteoarthritis-related pain at the base of their thumb. Participants applied nettle leaf (Urtica dioica) daily for one week to the painful area. The effect of this therapy was compared with that of placebo, Lamium album  (white deadnettle leaf), for one week after a 5-week washout period. After one week’s therapy with nettle sting, score reductions on both visual analogue scale and health assessment questionnaire were significantly greater than with placebo.

Stinging nettle leaf extracts lessen inflammation, in part, by suppressing the release of inflammatory cytokines. They do this by blocking a chemical inducer known as NF-KappaB, which alters gene expresion. This may be one explanation for the favorable effects has exhibited in rheumatoid arthritis. The Journal of Rheumatology reported Dec 1999 the findings of a study by S. Klingelhoefer et al on the antirheumatic effect of IDS 23, (a nettle leaf extract), on in vitro expression of T helper cytokines. They concluded “may inhibit the inflammatory cascade in autoimmune diseases like rheumatoid arthritis.”  The nettle leaf extract IDS 30 has been recommended for adjuvant treatment of rheumatic diseases. April 2002, published a report about a study of the immmunosuppressant activity of IDS 30, on myeloid dendritic cells in vitro. The nettle extract IDS 30 has prevented the maturation of dendritic cells leading to reduced induction of primary T cell responses. Dendretic cells play an important role in the initiation of rheumatoid arthritis. Nettle extract was able to keep dendretic cells from growing, however did not kill the cells.

Spirulina Helps Boost Immunity

Spirulina (also called blue-algae) may boost your immune system by increasing antibody production in response to pathogens. These algae was found to increase immune response through enhanced production of the immunoglobulin IgA, interleukin-6 and interferon-gamma. Also, enhances immunity through increased phagocytic activity of macrophages, stimulates production of antibodies and cytokines, increases accumulation of natural killer cells in tissue, and activates and mobilizes T and B cells.

Spirulina Benefits and Immune System

Spirulina activates very of the several immune cells, including macrophages, T-cells, B-cells, and natural killer cells. Besides, activates the organs involved with immune function such as the spleen, liver, bone marrow, and thymus gland. In vitro experiments found that spirulina had antiviral activity against cytomegalovirus, mumps, measles, influenza A viruses, HIV and herpes simplex. Researchers discovered that it not just stimulates the immune system, also, improves the body’s ability to generate new blood cells.

In 1979, Russian researchers reported first research on the immune stimulating effects on rabbits from lipopolysaccharides in spirulina. More new researches in Japan and China have shown polysaccharide extracts increased macrophage function, antibody production and infection-fighting T-cells. Natural killer cells target and kill cancer in the body as well as enhance the ability to fight off disease. Some clinical trials have shown that spirulina may help the immune system fight off cancer cells by increasing NK (natural killer) cells. Two preliminary studies using spirulina at 400mg daily noted that natural killer cell activity increased by 40% and mRNA production of natural killer cells increased by 37-55% after a week of supplementation. Spirulina significantly increases cytokine production in cultured immune system cells, according to a research reported in the Fall edition of the “Journal of Medicinal Food“. According to a study reported in October 2005 in the Current Pharmaceutical Biotechnology; spirulina develops the activity of white blood cells, stimulates antibodies and enhances the number of natural killer cells.

At the 30th Annual Meeting of the Japanese Society for Immunology held in Nov, 2000, researchers from the “Osaka Institute” reported a spirulina clinical study. In the study, spirulina significantly increased the tumor-killing ability of natural killer cells and interferon-gamma in participants aged 40 and above, and it continued for  12 to 24 weeks after stopping the administration of spirulina. A new twelve-week study involving 30 participants over 50 who took Hawaiian Spirulina Pacifica, produced by Cyanotech, found improved immune blood markers in the majority of participants. The study found a steady improve in haemoglobin in both sexes with women benefiting more rapidly. Furthermore, found improved immune blood markers in the majority of participants.

The radioprotective properties of an extract of  Spirulina platensis has been investigated using the micronucleus test in polychromatic erythrocytes of bone marrow of mice. In this system the extract caused a important decreased of the micronucleus frequencies induced by gamma-radiation. Spirulina has a dark blue-green color, because it is rich in a brilliant blue polypeptide called phycocyanin, which affects the stem cells found in bone marrow. Researches show that phycocyanin affects the stem cells found in bone marrow. Phycocyanin also stimulate hematopoiesis, simulating the effect of the hormone erythropoietin. Hormone erythropoietin. is produced by healthy kidneys and regulates bone marrow stem cell production of red blood cells. Phycocyanin  regulates production of white blood cells, even when bone marrow stem cells are damaged by toxic chemicals or radiation. Based on this property, spirulina is approved in Russia for treating radiation sickness. This nutrient was shown to correct the immune cell parameters in a study with children exposed to prolonged low dose radiation in Chernobyl. In all the children an improve in T-lymphocytes and T-helper cells was seen, and T-suppressor cells were normalized. IgA levels became normal. In an animal-based study, spirulina was shown to modulate radiation induced hematological and biochemical alterations. Swiss Albino mice were exposed to gamma radiation. The average hemoglobin, total erythrocyte count and total leucocyte count were elevated in the group receiving spirulina.

Spirulina Against HIV

Compounds isolated from spirulina inhibit the replication of HIV in test-tube studies. A study reported in the Journal of Acquired Immune Deficiency Syndrome found that the use of spirulina inhibited HIV replication in the blood. Taking extract concentrations between 0.3 and 1.2 micrograms per milliliter reduced viral production by approximately 50 %. In 1989, the results of a study in vitro, demonstrated that sulfoglycolipids in blue-green algae (like spirulina) exhibited powerful antiviral activities. Other study, reported in the “Journal of Natural Products“, demonstrated that Ca-SP (Calcium Spirulan), a spirulina polysaccharide extract, too has antiviral effects. Recent studies indicate that spirulina also presents clinically important anti-viral and immuno-stimulating effects in people infected by HIV. A study conducted in Cameroon and reported on the May 2011 in “Nutrition and Metabolic Insights” showed the nutritional efficiency of spirulina in terms of weight gain in HIV-infected malnourished patients.

Spirulina Joins Cancer Fight

Spirulina is a type of blue-green algae. These algae produces body chemicals that attack tumor cells that cause cancer. Test tube and animal-based studies indicate spirulina may boost the immune system and anticancer effects.

Spirulina Cancer Benefits

Spirulina strengthens the immune system to fight against the formation of malignant tumors. In a 2002 Japanese study, twelve male participants were administered an oral hot water extract of spirulina, and the number and activity of their natural killer cells was measured before and after therapy. At the end of the study period, there was a significant increase in the production and cancer-killing ability of these participants’ natural killer cells. A study performed by a Chinese scientists reported in Biomedicine and Pharmacotherapy in Oct 2009, show that a combination of selenium and Spirulina plantesis may have the effect to avoid human breast cancer. A 2002 study by the Department of Animal Sciences at India’s University of Hyderabad from the US National Institutes of Health’s research data publication site, explains the process by which spirulina is able to inhibit the elevated levels of Cycloxygenase-2 associated with inflammation and cancer.

In mice with chemically induced stomach cancer, the tumor burden was reduced to half that of the control animals using high-dose spirulina therapy. Experimental studies in animal models have showed an inhibitory activity of spirulina on oral carcinogenesis. Preliminary study findings show that taking 1 g of spirulina fusiformis daily by mouth for 12 months reduces oral leukoplakia (a non-cancerous, but high risk pre-cancerous condition) in individuals who chew tobacco. According to a 1995 study published in “Nutrition and Cancer“, 45% of Indian patients who chewed tobacco reported a complete regression of pre-cancerous mouth lesions after receiving extracts of spirulina for 12 months. Spirulina has chemo-protective and radio-protective effect, and may be a potential adjunct to cancer treatment. Researchers in China have shown that spirulina increased the level of white cells in the blood and of nucleated cells and DNA in the bone marrow of mice that had been subjected to radiation and chemotherapy.

C-PC (C-phycocyanin) from Spirulina has been previously shown to have anti-cancer effects. It is a water soluble, non-toxic fluorescent protein pigment with strong antioxidant, anti inflammatory and anticancer activities. In a study the effect of highly purified C-Phycocyanin was investigated on growth and multiplication of human chronic myeloid leukemia cell line. The results demonstrate important reduction (49%) in the proliferation of K562 cells treated with 50 microM C-Phycocyanin  up to 48 hour. Researchers at the “Osaka Institute of Public Health” have found that spirulina extrac promoted the activation of natural cancer-fighting substances in the body. In this study participants over 40 years of age were given 50 ml of a spirulina extract (Lina Green 21) and the level of natural cancer-fighting substances were measured in their blood. The findings demonstrated that spirulina extract significantly increased the tumor killing ability of  NK (natural killer) cells and interferon gamma. The interferon gamma and NK cell activity was increased 1-2 weeks after administration of spirulina and the activity continued for 12-24 weeks  after stopping the administration of spirulina.

Spirulina has a dark blue-green color, because it is rich in a brilliant blue polypeptide called phycocyanin, which affects the stem cells found in bone marrow. Phycocyanin builds blood. Chinese researchers documented phycocyanin as stimulating hematopoiesis, emulating the affect of the hormone erythropoetin (EPO). Chinese researchers claim phycocyanin also regulates production of white blood cells, even when toxic chemicals or radiation damages bone marrow stem cells. Based on this property, spirulina is approved in Russia for treating radiation sickness. These algae was  used to treat children suffering radiation sickness after the Chernobyl disaster. Their bone  marrow is damaged, rendering them immunodeficient and unable to produce normal red or white blood cells. Children fed only 5 g of Spirulina tablets each day make impressive recoveries within 6 weeks. Children not given spirulina remain diseased. Research continuing through 1999 in Belarus demonstrated immune building, normalization of peroxide lipid oxidation and detoxifying effects of spirulina extract in children and teenagers.