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Finasteride :( Proscar , Propecia ) Propecia is a licensed medicine for the treatment of men with male pattern baldness (androgenetic alopecia) to increase hair growth and prevent further hair loss. Propecia is not licensed for use in women, However , numerous studies had show results in women too . Propecia works in the scalp affecting the conversion of testosterone Propecia inhibits the production of DHT, which in most men bring the Propecia has been studied in several tests including a 5 year clinical study which gave the following results.
According to the clinical studies, Propecia showed very few side effects that too very rarely and did not affect most men. A small number of men had sexual side effects, with each happening In common use, the following mild and less serious side effects have Propecia is as such a very safe and effective drug, but you have to
Minoxidil ( Rogaine , Rogaine Foam , etc ) : Minoxidil is the generic name for products originally developed by UpJohn and called Rogaine in the USA or Regaine in Europe and elsewhere. Rogaine and Regaine are the trade marks of UpJohn Inc., USA. Rogaine and Regaine are exactly the same but simply packaged in differently. The FDA would not allow UpJohn to call their product Regaine in the USA as it implies hair regrowth (Re-Gain) whereas the FDA regards Minoxidil as a hair loss prevention drug. UpJohn had to change the name to Rogaine before receiving the FDAs approval to sell the product in the USA. First introduced in 1988, Rogaine was originally only available on prescription and used under the supervision of a doctor. However, extensive trials by UpJohn convinced the FDA to pass Minoxidil as acceptable to sell over the counter direct to the public. Rogaine or Regaine 2% concentration is widely available throughout the USA and Europe and it is the only proven hair loss treatment available without prescription. For many years Minoxidil was only available as a 2% concentration and exclusively from UpJohn as they held the patent rights. The patent ended in 1996 and since then several other drug companies have started to produce and sell Minoxidil 2% under many different brand names at a lower price than UpJohn. As of 3 July 1998, the distributors of 2% Minoxidil registered with the Federal Drug Administration are; Alpharma, Bausch and Lomb, Copley Pharm, Hi Tech Pharma, Morton Grove, Sight Pharms, Teva, and of course Pharmacia and Upjohn. These manufacturers/distributors supply pharmacies and supermarkets with Minoxidil in a wide variety of packaging as retailers require. In response to losing the patent on Minoxidil 2% UpJohn embarked on clinical trials of a 5% concentration solution. This is now available over the counter in the USA as Rogaine extra strength. UpJohn retains a new patent on this 5% concentration. However, it is possible to buy 5% Minoxidil solutions from other manufacturers. The solution usually has extra ingredients to distinguish it from UpJohn's product and circumnavigate any patent lawsuit brought by UpJohn. Minoxidil for hair loss is used as a topical application. The drug is dissolved in a mixture of water, alcohol and glycol which is applied to bald regions of the scalp as directed by the manufacturers. For men it is believed most effective for hair regrowth on the vertex rather than for treating hair loss at the temples. Minoxidil is a stable and inactive drug. When it is applied to the scalp and penetrates into the skin it must be converted to an active, but unstable, product called Minoxidil sulphite. Our body produces a catalyst called sulfonyl transferase that converts the stable inactive Minoxidil into the unstable active Minoxidil sulfite. Minoxidil sulfite activates potassium channels in cells and this leads to hair growth. The exact molecular mechanism operating in the cells that results in hair growth is not known. Some have suggested that minoxidil, as a known vasodilator, dlilates the blood vessles around hair follicles and the increased nutrient supply permits increased hair growth. However, this is an unlikely explanation as other vasodilator drugs do not promote hair growth and studies have shown no significant changes in scalp blood supply when using minoxidil. Topical minoxidil apparently induces an increased rate of DNA synthesis in follicular cells in early anagen, but not in nonfollicular cells such as fibroblasts or epidermal keratinocytes. Minoxidil induces a significant increase in DNA synthesis in all hair follicle cells in a dose-specific manner. Recently, researchers at L'Oreal suggested that minoxidil works by activating PGHS 1 (prostaglandin endoperoxide synthase-1) which may help promote hair growth.
Why does minoxidil work better for women than for men It may be that minoxidil is better able to penetrate the skin of women compared to men. The potential for greater drug penetrance is shown by the increased risk of systemic hair growth occurring in women using minoxidil compared to men. This is the reason why 5% minoxidil is not recommended for use by women. Women using 5% minoxidil in clinical trials were inclined to grow hair in areas where minoxidil was not applied. This suggests minoxidil is more likely to get into the blood stream of women and cause systemic hair growth as compared to men. This could be a dangerous situation as minoxidil is a vasodilatory drug used orally to treat blood pressure problems. Someone with normal blood pressure who takes minoxidil that enters the blood stream may develop low blood pressure. In addition, the female hair loss pattern makes hair growth more likely with any treatment. Female pattern baldness is usually a diffuse thinning rather than recession of the hair line. The thinning hair involves a gradual reduction in size of the hair follicles and these types of follicles are ideal for minoxidil products to have greatest effect.
Dutasteride Dutasteride and finasteride are both 5-alpha-reductase (5AR) inhibitors. Both treatments work by inhibiting 5AR, the enzyme responsible for converting testosterone to dihydrotestosterone (DHT). DHT is the primary androgen in the prostate. It is a primary factor in the development and progression of benign prostatic hyperplasia (BPH) and other prostate diseases and is also a major cause of hair loss. Dutasteride is a competitive inhibitor of both type-1 and type-2 isoenzymes of DHT, with 45-fold greater potency than finasteride against type-1 and type-2 isoenzymes. Approximately 85% to 90% of DHT is suppressed by the inhibition of type-2 isozymes. The remaining DHT is hypothesized to be from type-1 5-alpha-reductase. Finasteride is a competitive inhibitor of 5-alpha-reductase that selectively inhibits the type-2 isoenzyme. The dual inhibition resulting from dutasteride treatment may be beneficial for treat male pattern baldness better than Finasteride .
Ketoconazole
Ketoconazole is a relatively new and particularly potent anti androgen drug. Since 1985 there have been various studies suggesting that ketoconazole could be used to treat androgenetic alopecia as well as hirtusim .. Ketoconazole works by blocking the production of hormones by the gonads and the adrenal glands when it is take orally .Also , the important of this drug is that it works topically ( apply it as a cream or as a lotion ) but ,what it is even more unique , is that also works apply it as a shampoo ( Nizoral ) Ketoconazole comes in three basic forms; Nizoral cream 2%, Nizoral shampoo 2%, and Nizoral tablets all are made by Janssen Pharmaceutica , also there are several generic version and a new Foam version named Extina. The shampoo is a bright red color where the active ingredient is a 2% concentration of the antifungal Ketoconazole, an imidazole derivative. Ketoconazole acts to stop the formation of fungal cell membranes. The shampoo is used to treat dandruff where it is believed fungal infection can exacerbate the condition. Both shampoo and cream are used for skin fungal infections. These topical applications are tolerated very well and rarely have side effects. The tablets are used for systemic fungal infections. Oral use has been associated with potential side effects including hepatotoxicity. This has led to death in a few individuals who took too much of the drug. Consequently, people using the tablets are very carefully monitored. Headache, fever, and hypersensitivity have also been suggested as potential side effects of tablet use. Although Ketoconazole is officially an antifungal agent it has also been shown to lower serum testosterone when taken in tablet form. As a result some people with androgenetic alopecia have used the drug in an attempt to counteract hair loss by reducing free testosterone. Other individuals use the cream and/or shampoo in the hope of locally reducing the testosterone levels around hair follicles. However, no research has been conducted to show whether topical application is truly effective in treating androgenetic alopecia
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