α-adrenoceptor antagonists in the treatment of benign prostate hyperplasia

被引:37
作者
Thiyagarajan, M [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res, Dept Pharmacol & Toxicol, Mohali 160062, India
关键词
benign prostate hyperplasia; alpha-adrenoceptor antagonists; lower urinary tract symptoms;
D O I
10.1159/000058037
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Benign prostate hyperplasia (BPH) is a common malady affecting elderly men throughout the world, and it is the most common cause of voiding dysfunctions in man. The disease becomes prevalent, as the mean age of the population increases. In BPH the glandular cells and myofibroblasts of periurethral and transition zones proliferate excessively. This excessive growth of tissue mass physically compresses the urethra, leading to urinary obstruction and lower urinary tract symptoms (LUTS). Another major factor that contributes to LUTS in BPH is the increase in smooth muscle tone, a dynamic component. Contraction of the prostate gland is mainly under the control of the autonomic system and is mediated through alpha-adrenoceptors. In addition to alpha(1)-adrenoceptors, there are many other components that influence growth and contraction of the prostate gland, resulting in the development of BPH and LUTS. The prostate gland is contracted on stimulating 5-HT, endothelin, tachykinin, and muscarinic cholinergic receptors. Growth of the prostate gland is under the control of androgens, endothelin growth factor, vasoactive intestinal peptide, nerve growth factor, and growth hormone. The combination of excessive growth and the tone produced by different components results in LUTS and BPH. alpha(1)-Adrenoceptor antagonists were successfully used in the treatment of BPH to relieve the LUTS. The high selectivity Of alpha(1A)-adrenoceptor antagonists reflects the uroselectivity. The uroselective compounds like terazosin, doxazosin, tamsulosin, and alfuzosin are in clinical use. Other new potent uroselective compounds, which are analogs of nigulidipine, 5-methyl-urapidil, or naftopidil, are in clinical trials. In addition to alpha-antagonists, antiandrogens (5alpha-reductase inhibitors) and polyherbal formulations are used to treat BPH. The success of BPH treatment lies in the development of new chemical entities which are efficacious as well as more uroselective and hence have least side effects. Copyright (C) 2002 S. Karger AG, Basel.
引用
收藏
页码:119 / 128
页数:10
相关论文
共 81 条
[1]   Endothelin receptors in testosterone-induced prostatic hypertrophy in rats [J].
Auger-Pourmarin, L ;
Roubert, P ;
Chabrier, PE .
JAPANESE JOURNAL OF PHARMACOLOGY, 1998, 77 (04) :307-310
[2]   RELATIONSHIP OF SYMPTOMS OF PROSTATISM TO COMMONLY USED PHYSIOLOGICAL AND ANATOMICAL MEASURES OF THE SEVERITY OF BENIGN PROSTATIC HYPERPLASIA [J].
BARRY, MJ ;
COCKETT, ATK ;
HOLTGREWE, HL ;
MCCONNELL, JD ;
SIHELNIK, SA ;
WINFIELD, HN .
JOURNAL OF UROLOGY, 1993, 150 (02) :351-358
[3]   LIGHT MICROSCOPIC STEREOLOGICAL ANALYSIS OF THE NORMAL HUMAN-PROSTATE AND OF BENIGN PROSTATIC HYPERPLASIA [J].
BARTSCH, G ;
MULLER, HR ;
OBERHOLZER, M ;
ROHR, HP .
JOURNAL OF UROLOGY, 1979, 122 (04) :487-491
[4]  
BARTSCH G, 1989, UROLOGE A, V28, P321
[5]   DISTRIBUTION OF BETA(3)-ADRENOCEPTOR MESSENGER-RNA IN HUMAN TISSUES [J].
BERKOWITZ, DE ;
NARDONE, NA ;
SMILEY, RM ;
PRICE, DT ;
KREUTTER, DK ;
FREMEAU, RT ;
SCHWINN, DA .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1995, 289 (02) :223-228
[6]   THE DEVELOPMENT OF HUMAN BENIGN PROSTATIC HYPERPLASIA WITH AGE [J].
BERRY, SJ ;
COFFEY, DS ;
WALSH, PC ;
EWING, LL .
JOURNAL OF UROLOGY, 1984, 132 (03) :474-479
[7]   Toward the development of α1a adrenergic receptor antagonists [J].
Bock, MG ;
Patane, MA .
ANNUAL REPORTS IN MEDICINAL CHEMISTRY, VOL 35, 2000, 35 :221-230
[8]  
Boehm S, 1998, WIEN KLIN WOCHENSCHR, V110, P817
[9]   TREATMENT OF CHRONIC PROSTATITIS AND PROSTATODYNIA WITH POLLEN EXTRACT [J].
BUCK, AC ;
REES, RWM ;
EBELING, L .
BRITISH JOURNAL OF UROLOGY, 1989, 64 (05) :496-499
[10]   ADRENERGIC AND CHOLINERGIC RECEPTORS IN HUMAN PROSTATE, PROSTATIC CAPSULE AND BLADDER NECK [J].
CAINE, M ;
RAZ, S ;
ZEIGLER, M .
BRITISH JOURNAL OF UROLOGY, 1975, 47 (02) :193-202