Guest guest Posted October 1, 2003 Report Share Posted October 1, 2003 Hi All, & Hi Sammy, Sammy, Many thanks for the fine summary of BPH throught to PC. Could I have your permission to cross-post to the Chinese Herb Academy List? CHA has >800 herbalists on board. IMO, a discussion of current attempts to treat BPH and PC with herbal medicine and/or acupuncture would be very useful. Best regards, Phil >>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>> <ga.bates Date sent: Tue, 30 Sep 2003 23:38:28 +0100 Ken and All, The prostate is a primary male sexual characteristic having its embryological origins as described previously by Emmanuel " It is the male organ which is homologous with (embryologically from the same tissue as) the female uterus " . During growth the male prostate differentiates itself from the female uterus by morphological changes which position it at the base of the bladder and through which the urethra passes. Manual examination or digital rectal examination (DRE): When fully developed the prostate is a small walnut shaped muscular gland which may be digitally palpated via the colonic mucosa. A normal prostate should feel solid, smooth and round without asymmetry. Observing standard clinical practice (surgical glove and anti-friction gel), a normal palpation of the prostate with the fingertip should not be painful. After maturation the prostate consists of both muscle and glandular tissue (similar to the breast) and provides a thick milky fluid (semen) to help express sperm cells into the vagina. The prostate sits upon the urethra and it is from the prostate and seminal vesicles that prostatic fluid is pumped during orgasm. Because of variations in sexual activity during the life time of the male the prostate is capable of undergoing changes in size to maximise reproductive capacity at crucial times and minimise energy loss and wasteful sexual activity during less critical periods (e.g. during times of seasonal hardship). These changes in prostate size do not normally affect urinary function. Hormone receptors in prostatic tissue respond to growth triggers during puberty and thereafter. Secondary sexual growth inhibition factors impose limits on the size of the prostate despite high levels of androgen in the young sexually active male. From the thirties onward in many men the prostate undergoes changes that reflect ageing. Various processes including capillary atherosclerosis, urinary reflux and virus infection contribute to a benign prostatic hyperplasy (BPH - or prostatic enlargement) that may impact on free passage of urine through the organ. Prostatic interepithelial neoplasia (PIN) is believed to occur after BPH induced cellular breakdown facilitates leakage of prostatic cell- fragments into the rich growth supporting environment of prostatic fluid stored in the organ and the seminal vesicles. A final stage to prostatic carcinoma (PC) may be facilitated by changes in the male sex-steroid hormone mileau which interfere with the normal homeostatic processes controlling prostate size and cellular response to growth triggers. Despite occult PC being age-dependent with a consistent distribution across cultures worldwide, there is a strong tendency in western society for the disease to become manifest and often fatal. Men of African descent living in the west have a higher incidence of PC. This probably reflects socio-economic, cultural and life-chance patterns, rather than a racial connection. Indeed, there is no evidence that Africans, or any other rural group from the Eskimo to the Bushman are more (or less) prone to PC regardless of ethnic dietary preferences for meat or fat or carbohydrates in the context of daily subsistence living. By contrast second and third generation diaspora acquire the same (or worse) tendency to PC in the context of a western diet and lifestyle. Many contributing factors to carcinogenesis have been postulated from xenoestrogenic pesticides and packaging plastics to the 'male menopause' and the disruption of male hormones in the workplace. Symptoms of BPH may often go unnoticed until an incident (perhaps through stress or infection) precipitates subjective awareness of dysuria: for example nocturia, latency; or inability to 'pee' with a full sensation, dribbling and pain in the urethra. PC itself may be associated with pain on ejaculation and blood in the urine. However, many cases of fully blown metastatic PC occur without prior warning. PC metastasises to the bone generally in the lower back and to the lymph nodes. Some western texts now associate PC with low back pain and weakness in the legs - text book Kidney Yin deficiency - a TCM influence that has not had its full potential realised. In the 1950's it was discovered that death due to metastatic PC could be averted by five years or more by bilateral orchietomy. Since then the procedure has become commonplace, and in some countries mandatory NHS treatment for advanced PC. Albeit castration removes the hormonal impulse of prostatic tissue to grow this is only a temporary palliation since the condition returns in an androgen independent form (AIPC). Because of its unpleasantness alternatives treatments to castration have always been sought. Modern gene manipulation techniques hold some hope in the distant future, but the mainstays are still surgery and radiation which may remove local disease. Once the PC is said to have 'breached the prostatic capsule' and become systemic, local therapy is useless and hence the continued need for castration to palliate the condition. Sadly, many men with PC end their days being castrated either physically or chemically. Chemical castration agents block the production of testosterone (e.g. estrogens which lead to feminisation) or anti-androgens (AA) which block sex-steroid cell receptors. A class of drug known as luteinising hormone releasing hormone agonist analogs (LHRH-a) is used to inhibit testosterone production by a 'crowbar effect' on the hypothalamus-pituitary. All forms of androgen suppression lead to serious side effects in men including bone demineralisation, muscle loss, affective and cognitive disorders including Alzheimer's disease. Detection: The 'PSA' or prostate specific antigen is a protein detected in blood which normally resides within the healthy prostatic cell. Once PSA is detectable in significant amount in the blood it is generally accepted that PC is present although small amounts may indicate BPH [ range 0 - 4 ng/ml normal to 40 years of age and then add 2 ng/ml per decade until 80 years.] A PSA > 20 ng/ml is generally regarded as indicative of PC at any age. The 'free PSA' is a measure of bound and unbound PSA proteins and is held to be more reliable than the 20 ng/ml ceiling. Staging: PC itself may be described by the TNM staging method as well as what is known as Gleason Score (GS) which is histologically determined based on cellular architecture - the higher the Gleason Number [ range 0 - 5 ] the less differentiated the cell. A Score is obtained by determining the two most frequent cellular architectures and adding. Gleason Scores between 0 - 10 are then possible. A GS is believed to predict fairly accurately patient survival: a GS 10 being the least prognostically hopeful. Prognostic distinctions for a particular GS are commutative: so for example a GS [ 3 + 4] = 7 is different from a GS [ 4 + 3] also = 7 [ In this case the 3+4 is prognostically better than the 4+3]. Most western cancer agencies are now recommending that all men over the age of 50 undergo a DRE and PSA test. Individuals with a family history or members of certain racial populations (Africans) are advised to start testing at age 40. PC can be treated successfully if detected early and given appropriate timely treatment. Some men however prefer not to know what their PSA is due to a possible false positive indication, and in order to avoid potentially destructive side effects of treatment. This position is also taken by some governments as a cheap alternative to national screening programmes that will appeal to the ignorant and uninformed. Failure to treat PC may lead to premature death. In the UK 1000 men under the age of retirement die of PC every year. In the USA the figure is about 5000. About 50,000 men in all die of prostate cancer every year in the USA, 10,000 in the UK. I hope this has helped TCM students appreciate the importance of this disease in the west. There are many informational pages on prostate cancer available on the internet. They all have an agenda of one sort or another from the persuasive pieces written by the doctor trying to recruit another patient for his clinic to the pharmaceutical company eager to demonstrate how effective their brand of treatment can be. This piece has been written with the inside knowledge of one who has survived the condition for seven years as a non-castrate. I am trying to translate my survival perience into something that will make sense on both sides of the east-west conventional-traditional divide. Unfortunately modern medicine knows as much about natural hormone control as traditional medicine knows about sex-steroid synthesis. Just as modern physics needed a Heisenberg to crystallise the uncertainties of quantum mechanics, so we need a master alchemist who will fuse ancient and modern into a brand new paradigm. A successful treatment that did not impact on male quality of life would certainly put TCM on the map and it is something I advise any ambitious student to put his or her mind to. It is getting late now and I have spent most of the evening putting this together. At some time in the future I'll take a look at the existing TCM treatments for PC. In the meantime you might like to take a look yourself at PC-SPES a very famous TCM/WM recipe that really clobbered PSA and then got clobbered itself by the FDA for its pains; or, Equiguard the big promise that never seemed to materialise. Or perhaps some of the more recent treatments Vervain for instance (is it just another estrogen analogue ?) or Sarcandra - does it really reduce prostatic inflammation ? What about DIM the Great White Hope ? [ No I am not being an inverted racialist, DIM is made from extract of white cabbage ;-] Cheers, Sammy. >>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>> Best regards, Email: < WORK : Teagasc Research Management, Sandymount Ave., Dublin 4, Ireland Mobile: 353-; [in the Republic: 0] HOME : 1 Esker Lawns, Lucan, Dublin, Ireland Tel : 353-; [in the Republic: 0] WWW : http://homepage.eircom.net/~progers/searchap.htm Quote Link to comment Share on other sites More sharing options...
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