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1.
Urology ; 57(5): 999-1005, 2001 May.
Article in English | MEDLINE | ID: mdl-11337315

ABSTRACT

OBJECTIVES: To determine the effects of a saw palmetto herbal blend (SPHB) compared with finasteride on prostatic tissue androgen levels and to evaluate needle biopsies as a source of tissue for such determinations. METHODS: Prostate levels of testosterone and dihydrotestosterone (DHT) were measured on 5 to 10-mg biopsy specimens (18-gauge needle cores) in three groups of men with symptomatic benign prostatic hyperplasia: 15 men receiving chronic finasteride therapy versus 7 untreated controls; 4 men undergoing prostate adenomectomy to determine sampling variability (10 specimens each); and 40 men participating in a 6-month randomized trial of SPHB versus placebo, before and after treatment. RESULTS: Prostatic tissue DHT levels were found to be several times higher than the levels of testosterone (5.01 versus 1.51 ng/g), that ratio becoming reversed (1.05 versus 3.63 ng/g) with chronic finasteride therapy. The finasteride effect was statistically significant for both androgens (P <0.01), and little overlap of individual values between finasteride-treated and control patients was seen. In the randomized trial, tissue DHT levels were reduced by 32% from 6.49 to 4.40 ng/g in the SPHB group (P <0.005), with no significant change in the placebo group. CONCLUSIONS: For control versus finasteride-treated men, the tissue androgen values obtained with needle biopsy specimens were similar-both for absolute values and the percentage of change-to those previously reported using surgically excised volumes of prostatic tissue. The quantification of prostatic androgens by assay of needle biopsies is thus feasible and offers the possibility of serial studies in individual patients. The SPHB-induced suppression of prostatic DHT levels, modest but significant in a randomized trial, lends an element of support to the hypothesis that inhibition of the enzyme 5-alpha reductase is a mechanism of action of this substance.


Subject(s)
Androgen Antagonists/pharmacology , Dihydrotestosterone/analysis , Enzyme Inhibitors/pharmacology , Finasteride/pharmacology , Plant Extracts/pharmacology , Prostate/chemistry , Prostate/drug effects , Prostatic Hyperplasia/drug therapy , Testosterone/analysis , Aged , Androgen Antagonists/therapeutic use , Biopsy, Needle/statistics & numerical data , Enzyme Inhibitors/therapeutic use , Finasteride/therapeutic use , Humans , Male , Middle Aged , Placebos , Plant Extracts/therapeutic use , Prostate/pathology , Prostatic Hyperplasia/pathology , Serenoa , Treatment Outcome
2.
Public Health Nutr ; 3(4A): 447-52, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11276292

ABSTRACT

A brief discussion of the history of the use of herbal medicines from prehistoric times to the mid-twentieth century precedes an explanation of why usage of such remedies in the United States declined in the 1940s but returned to popularity in the 1980s. The provisions of the Dietary Supplement Health and Education Act of 1994 are presented together with its perceived influence, both positive and negative, on the health of the American people. Possible futures of herbal medicines are considered. The negative viewpoint that they will ultimately be rejected is refuted, and the more optimistic prediction that herbs are ultimately destined to become a part of mainstream medicine is defended. Stumbling blocks to such acceptance are evaluated and methods of overcoming them suggested. The urgent need for the development of a sensible regulatory environment encouraging the approval of botanicals as drugs is emphasized. After predicting a bright future for rational phytomedicines, the author opines that many of them will eventually play significant roles in medicinal practice.


Subject(s)
Legislation, Drug/trends , Phytotherapy/history , Plants, Medicinal/therapeutic use , Europe , Forecasting , History, 19th Century , History, 20th Century , History, Ancient , History, Medieval , Humans , Legislation, Drug/history , Plants, Medicinal/adverse effects , United States , United States Food and Drug Administration
3.
J Urol ; 163(5): 1451-6, 2000 May.
Article in English | MEDLINE | ID: mdl-10751856

ABSTRACT

PURPOSE: We tested the effects of a saw palmetto herbal blend in men with symptomatic benign prostatic hyperplasia (BPH) via a randomized, placebo controlled trial. MATERIALS AND METHODS: We randomized 44 men 45 to 80 years old with symptomatic BPH into a trial of a saw palmetto herbal blend versus placebo. End points included routine clinical measures (symptom score, uroflowmetry and post-void residual urine volume), blood chemistry studies (prostate specific antigen, sex hormones and multiphasic analysis), prostate volumetrics by magnetic resonance imaging, and prostate biopsy for zonal tissue morphometry and semiquantitative histology studies. RESULTS: Saw palmetto herbal blend and placebo groups had improved clinical parameters with a slight advantage in the saw palmetto group (not statistically significant). Neither prostate specific antigen nor prostate volume changed from baseline. Prostate epithelial contraction was noted, especially in the transition zone, where percent epithelium decreased from 17.8% at baseline to 10.7% after 6 months of saw palmetto herbal blend (p <0.01). Histological studies showed that the percent of atrophic glands increased from 25. 2% to 40.9% after treatment with saw palmetto herbal blend (p <0.01). The mechanism of action appeared to be nonhormonal but it was not identified by tissue studies of apoptosis, cellular proliferation, angiogenesis, growth factors or androgen receptor expression. We noted no adverse effects of saw palmetto herbal blend. When the study was no longer blinded, 41 men elected to continue therapy in an open label extension. CONCLUSIONS: Saw palmetto herbal blend appears to be a safe, highly desirable option for men with moderately symptomatic BPH. The secondary outcome measures of clinical effect in our study were only slightly better for saw palmetto herbal blend than placebo (not statistically significant). However, saw palmetto herbal blend therapy was associated with epithelial contraction, especially in the transition zone (p <0.01), indicating a possible mechanism of action underlying the clinical significance detected in other studies.


Subject(s)
Androgen Antagonists/therapeutic use , Plant Extracts/therapeutic use , Prostatic Hyperplasia/drug therapy , Aged , Aged, 80 and over , Double-Blind Method , Humans , Male , Middle Aged , Prostatic Hyperplasia/pathology , Serenoa
4.
J Nat Prod ; 62(11): 1589-92, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10579884
7.
J Nat Prod ; 60(4): 417-8, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9134750

ABSTRACT

Brine shrimp lethality-directed fractionation of the 95% EtOH extract of the powdered, dried berries of Serenoa repens (Bart.) Small (saw-palmetto) (Palmae) led to the isolation of two monoacylglycerides, 1-monolaurin (1) and 1-monomyristin (2). Compounds 1 and 2 showed moderate biological activities in the brine shrimp lethality test and against renal (A-498) and pancreatic (PACA-2) human tumor cells; borderline cytotoxicity was exhibited against human prostatic (PC-3) cells. The fruits and extracts of saw-palmetto are taken orally as an herbal medicine to prevent prostatic hyperplasias.


Subject(s)
Antineoplastic Agents, Phytogenic/isolation & purification , Glycerides/isolation & purification , Laurates/isolation & purification , Myristic Acids , Plants, Medicinal/chemistry , Animals , Antineoplastic Agents, Phytogenic/pharmacology , Artemia , Glycerides/pharmacology , Glycerides/toxicity , Humans , Laurates/pharmacology , Magnetic Resonance Spectroscopy , Monoglycerides , Tetrazolium Salts , Thiazoles , Tumor Cells, Cultured
9.
J Am Pharm Assoc (Wash) ; NS36(1): 29-37, 1996 Jan.
Article in English | MEDLINE | ID: mdl-8835439
10.
11.
J Nat Prod ; 58(9): 1325-57, 1995 Sep.
Article in English | MEDLINE | ID: mdl-7494142

ABSTRACT

Until recently, the prevailing attitude in developed nations regarded the world's genetic resources, which are mainly concentrated in the developing world, as a common resource of humankind, to be exploited freely irrespective of national origin. With the devastation being wreaked in the tropical rainforests and the resurgence in interest in recent years in the discovery of novel drugs from natural sources, particularly plants and marine organisms, the international scientific community has realized that the conservation of these global genetic resources and the indigenous knowledge associated with their use are of primary importance if their potential is to be fully explored. With this realization has come a recognition that these goals must be achieved through collaboration with, and fair and equitable compensation of, the scientists and communities of the genetically rich source countries. The signing of the United Nations Convention on Biological Diversity by nearly all of the World's nations has emphasized the need for the implementation of such policies. In this review, the articles of the Convention of relevance to the activities and practices of the natural products scientific community are briefly discussed. This discussion is followed by a summary of policies for international collaboration and compensation being implemented by several developed country organizations, and the perspectives on the current developments given by representatives of some of the source countries located in the regions of greatest biodiversity.


Subject(s)
Biological Products/isolation & purification , Bioethics , Drug Industry , Ecosystem , International Cooperation , Plants, Medicinal , United Nations , United States
14.
JAMA ; 271(15): 1210, 1994 Apr 20.
Article in English | MEDLINE | ID: mdl-8151882
18.
Planta Med ; 54(2): 95-100, 1988 Apr.
Article in English | MEDLINE | ID: mdl-3043486
19.
Planta Med ; 53(1): 1-4, 1987 Feb.
Article in English | MEDLINE | ID: mdl-3554284
20.
J Nat Prod ; 50(1): 1-8, 1987.
Article in English | MEDLINE | ID: mdl-3298550
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