Posts Tagged ‘Central Nervous System’

How Does Ginseng Kill Cancer Cells?

December 31st, 2010
Susanna Ng asked:




Ginseng, a herbal medicine used extensively for centuries in oriental medicine including Chinese, Korean and Japanese as a general tonic to promote longevity can be effective in combating cancer, diabetes, stress, fatigues and oxidants. These effects of ginseng are mainly attributed to a group of compounds called ginsenosides, which recent studies indicate that they might act in a similar way as steroid hormones. A review of recent studies on ginseng was done by researchers from the UK, Hong Kong and China in a report published on the Chinese Medicine Journal. The report has unveiled the secret behind this longevity-enhancing herb.


What is ginseng? Ginseng is a deciduous perennial plant that belongs to the Araliaceae family. Currently, twelve species have been identified in the genus Panax. Among them, Panax ginseng C. A. Meyer (Araliaceae), cultivated in China, Korea, Japan, Russia, and the US, P. quinquefolium L (American ginseng), grown in southern Canada and the US and P. notoginseng, cultivated in Yunnan and Guangxi provinces in China, represent the three most extensively investigated species.

In modern times, ginseng is not only used as a therapeutic by traditional medical practitioners but is also as health supplements readily available in the commercial market.

“Recently, it has been found that ginsenosides can act as functional ligands to activate different steroid hormone receptors. Through such mechanisms, ginseng can exert its effects on the human body by acting in a similar way as the steroid hormones,” the researchers write.


What are the known effects of ginseng? The pharmacological and therapeutic effects of ginseng have been demonstrated to affect the central nervous system (CNS), cardiovascular system, endocrine secretion, immune function, metabolism, biomodulating action, anti-stress, and anti-aging. Recently, there have been controversies concerning the usefulness of ginseng in cancer therapy.

Most studies claimed that the pharmacological effects of ginseng are attributed to its bioactive constituents such as ginsenosides, saponins, phytosterols, peptides, polysaccharides, fatty acids, polyacetylenes, vitamins and minerals.

So how does ginseng make it? How does it combat cancers?

According to the Chinese Medicine Journal’s report, the anti-tumour effects of ginsenosides include its ability to induce cell death (such as apoptosis and necrosis), and having effects of anti-proliferation, anti-invasion and metastasis, and anti-angiogenesis.

Inducing cell death

Several compounds found in ginsenosides have been shown to induce apoptosis in prostate cancer cells, ovarian cancer cells, neuroblastoma cells and lung adenocarcinoma cells. The induction of tumour cell death by ginsenosides may be one of the mechanisms in the elimination of tumour cells, the writers say.

Anti-proliferation

Ginsenosides also have preventative effects by inhibiting the cell cycle progression. They have been shown to arrest the growth of human tumour cell lines in lung tumour cells, prostate carcinoma cells, leukuemia cells, and hepatoma (liver cancer) cells.

Anti-invasion and anti-metastasis

Cancer metastasis is a complex process involving angiogenesis and cell-cell interactions.


What is cancer metastasis? Metastasis is the spread of cancer from its primary site to other places in the body. Cancer cells can break away from a primary tumour, penetrate into lymphatic and blood vessels, circulate through the bloodstream, and grow in a distant focus (metastasize) in normal tissues elsewhere in the body.

Tumours are classified as either benign or malignant. Malignant tumours can spread by invasion and metastasis whilst benign tumours cannot (and only grow locally). Metastatic tumours are very common in the late stages of cancer. The spread of metastases may occur via the blood or the lymphatics or through both routes. The most common places for the metastases to occur are the adrenals, liver, brain and the bones. There is also a propensity for certain tumours to seed in particular organs.

Scientists recently demonstrated that the invasiveness of some endometrial cancer cells (including those of the uterus) was inhibited by treating them with a certain types of ginsenosides. The inhibitory effect is due to suppression of MMP-2 expression.


What are matrix metalloproteinases (MMPs)? MMPs are capable of degrading all kinds of extracellular matrix proteins. MMPs are also thought to play a major role on cell behaviours such as cell proliferation, migration (adhesion/dispersion), differentiation, angiogenesis, apoptosis and host defense.

The anti-invasive effects of several ginsenosides include the abilities to significantly inhibit in vitro invasion of hepatoma cells, melanoma cells, human lung carcinoma and pancreatic cancer cells. Ginsensodies have also been shown to inhibit lung metastasis, reduce the weight of tumours in lung, breast, gastric and melanoma cancers.

Anti-angiogenesis effects


What is angiogenesis? Angiogenesis is a physiological process involving the growth of new blood vessels from pre-existing vessels. Excessive angiogenesis has been defined as a prominent pathological feature of many diseases such as tumour, rheumatoid arthritis, atherosclerosis, psoriasis and diabetic retinopathy (“diabetic eyes”).

According to the present report, numerous recent studies have demonstrated several ginsenosides exert an anti-angiogenic action in different animal models when administered alone or in combination with other conventional chemicals, such as human breast infiltrating duct carcinoma, ovarian carcinoma cells, melanoma cells and colon carcinoma. These data indicate that one of the mechanisms of anti-metastatic effect of ginsenosides is probably related to suppression of tumour-induced angiogenesis.

A new class of anti-tumour drugs: ginsenosides Rg3 and Rh2?

The researchers say that both gensensides Rg3 and its metabolite form Rh2 have emerged in Mainland China and Taiwan as anti-cancer drugs in the form of capsules (e.g. ‘Rg3 Shenyi Jiaonang’ and ‘GOOD LIFE ginsenoside Rh2 capsule’). Rg3 Shenyi Jiaonang suppresses tumour angiogenesis and prevents adhesion, invasion and metastasis of tumour cells. Rh2 as an adjuvant agent was also tested in the nude mouse model with human ovarian cancer cells transplanted. In the presence of Rh2, cisplatin could significantly inhibit tumour growth in vivo and prolong survival time. Neither Rh2 nor cisplatin alone could inhibit tumour growth. It was shown that chemotherapy supplemented with Rh2 is 60% more effective than chemotherapy alone. It could also mitigate the adverse effects of hair loss, anemia, nausea, vomit and poor appetite following chemotherapy or radiotherapy.

Both Rg3 and Rh2 are extracted from red ginseng which is processed by steaming and drying. During the process, the malonyl group at the C-6 is released and the glycosyl moiety at C-20 is partially detached to generate Rh1, Rh2 and Rg3 through deglycosylation similar to the deglycosylated product, compound K generated from the metabolic transformation of ginsenoside Rb1 by intestinal bacteria. However, whether all of the ginsenosides generated by such post-treatment of white ginseng have similar anti-tumour effects are still not known.

[Chinese Medicine 2007, 2:6 doi:10.1186/1749-8546-2-6]

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Facts to Know About Muscle Relaxant

November 25th, 2010
Yury Bayarski asked:




Carisoprodol (also known under the brand name Soma) is a commonly prescribed muscle relaxant. It is chemically, structurally, and pharmacologically related to meprobamate. Meprobamate was a best-selling minor tranquilizer for a time, but has largely been replaced by the benzodiazepines.

Uses

Strains, sprains, and other muscle injuries can result in pain, stiffness, and muscle spasms. It is important to understand that muscle relaxants do not heal the injuries, but they do help to ease the discomfort and pain. Carisoprodol is prescribed along with rest, exercise, physical therapy, or other treatments for short-term relief of painful muscle conditions. Although the drug may provide prompt relief, it should never be considered a substitute for these other forms of treatment.

Carisoprodol works quite well for relieving muscle pain due to injuries, but is not effective for other types of pain.

Side effects

The most common side effects of carisoprodol are drowsiness, dizziness, agitation, nervousness, tremor, irritability, insomnia and nausea.

Because muscle relaxants work on the central nervous system, they may add to the effects of alcohol and other drugs that slow down the central nervous system, such as antihistamines, cold and allergy medicine, sleeping pills, medicine for seizures, some pain relievers, and other muscle relaxants.

How does it work?

Carisoprodol is a muscle relaxant that does not directly relax tense skeletal muscles. It acts by blocking electrical communication among nerves in the reticular formation of the brain and in the spinal cord. The pharmacological effects of the drug appear to be due to the combination of the effects of carisoprodol and meprobamate. The medication also has weak anticholinergic, antipyretic, and analgesic properties.

The drawback

The main disadvantage is its abuse and dependence potential. And the risk increases with prolonged use of the drug. A considerable portion of carisoprodol is metabolized to meprobamate, which is a known drug of abuse and dependence. However, a many physicians are unaware of the potential of carisprodol for abuse and of its metabolism to meprobamate.

Carisoprodol is a Schedule IV controlled substance in Arizona, Georgia, Hawaii, Florida, Kentucky, Massachusetts, Nevada, Oregon, but not a federally Schedule IV controlled substance. In the United States, the drug is available only with a physician’s prescription.

Carisoprodol, Fioricet, Tramadol

I Hurt All Over. How to Ease Away the Pain of Fibromyalgia!

May 18th, 2010
Nathan Wei asked:




At one moment, a life of activity consumed with enjoyable activities like biking, golfing, going to the movies, out to dinner. Then one day, it’s gone. Replaced with constant pain and fatigue. Here’s the lowdown on fibromyalgia.

Fibromyalgia is one of the most common forms of arthritis seen in a rheumatology practice. It is actually a soft tissue form of rheumatism. Typically, a patient will complain of feeling achy all over, being chronically tired, and feeling like they’re walking around in a constant fog. Often a patient will complain of short term memory problems.

The American College of Rheumatology has set criteria by which fibromyalgia symptoms can be classified. These consist of a history of widespread pain for three or more months and pain in 11 of 18 tender point sites when 4 kilograms (about 9 pounds) of pressure is applied. When accompanied by a history of chronic fatigue and non-restorative sleep (waking up and feeling as if you haven’t slept), there is a strong suspicion that fibromyalgia is to blame.

People affected by fibromyalgia experience two unique responses to stimuli. They perceive normal stimuli as being painful and they perceive painful stimuli as being more painful than it should be.

These abnormal responses are thought to be due to an abnormality involving pain-processing pathways within the central nervous system.

History and physical examination is the first step in evaluation. Unfortunately, there are no specific laboratory tests that confirm the diagnosis. However, the tests can be helpful in excluding other conditions that can mimic fibromyalgia such as hypothyroidism, lupus, and rheumatoid arthritis.

Treatment consists of a combination of four approaches. The first is patient education. Talking with the patient about the diagnosis and presenting what he options are. The second is institute medications. These may include one or more of the following:

o Analgesics which help to control pain. An example would be a drug such as tramadol

o Antidepressants which are used for their ability to elevate serotonin and nor-epiephrine levels in the brain. Examples include amitryptiline, fluoxitene, and duloxitene.

o Muscle relaxants like cyclobenzaprine

o Anti-seizure medicines like gabapentin

o Anti-fatigue medicines (modafinil)

The third therapy is non-impact aerobic exercise which helps to increase endorphin production in the brain and helps to recondition muscles.

Finally, the fourth is cognitive behavioral therapy which helps with goal-setting, coping and other measures which reduce the sense of victimization that people with fibromyalgia often have.

Fibromyalgia can be treated effectively. It is important that a patient seek out a qualified and empathetic rheumatologist to help them.

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