Yohimbine: a clinical review

被引:132
作者
Tam, SW
Worcel, M
Wyllie, M
机构
[1] Nitromed Inc, Bedford, MA 01730 USA
[2] URODOC, Herne Bay CT6 7LN, Kent, England
关键词
yohimbine; erectile dysfunction; sexual dysfunction; concomitant administration; blood pressure; alpha-adrenoceptors; combination therapy;
D O I
10.1016/S0163-7258(01)00156-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although yohimbine (YOH) has been available for the treatment of male erectile dysfunction (ED) for longer than Viagra(R), there is a perception that little is known about the clinical performance of the drug. This review attempts, by comprehensive analysis of the literature, to cover the clinical, pharmacological, and therapeutic profiles of YOH, relevant to its potential utility in the management of patients with ED. Relatively few well-designed studies have been completed. From these, however, it can be concluded that YOH as monotherapy possesses only modest efficacy in ED patients. In acute and chronic (long-term) studies, YOH has been found to be relatively free of side effects over the dose range predicted to be effective in ED. At much higher doses, the most frequently observed effects, consistent with the primary pharmacological action of the drug, are elevation of blood pressure, a slight anxiogenic action, and increased frequency of urination. These side effects are all easily reversible on termination of YOH therapy. There is increasing evidence that the erectogenic action of YOH can be augmented by concomitant administration of agents that augment the release and/or action of nitric oxide in the corpus cavernosum. YOH has yet to be studied in female sexual dysfunction. Overall, the benefit risk profile of YOH would indicate that it has potential, more probably as part of a combination strategy, e.g., with a drug that enhances the nitric oxide pathway, in the treatment of ED. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:215 / 243
页数:29
相关论文
共 153 条
  • [1] YOHIMBINE IMPAIRS P50 AUDITORY SENSORY GATING IN NORMAL SUBJECTS
    ADLER, LE
    HOFFER, L
    NAGAMOTO, HT
    WALDO, MC
    KISLEY, MA
    GIFFITH, JM
    [J]. NEUROPSYCHOPHARMACOLOGY, 1994, 10 (04) : 249 - 257
  • [2] AMANN FW, 1981, HYPERTENSION, V3, P119
  • [3] Effect of systemic alpha-2 adrenergic blockade on the morning increase in platelet aggregation in normal subjects
    Andrews, NP
    Goldstein, DS
    Quyyumi, AA
    [J]. AMERICAN JOURNAL OF CARDIOLOGY, 1999, 84 (03) : 316 - 320
  • [4] ARNER P, 1976, ACTA MED SCAND, V200, P273
  • [5] Ashton AK, 1997, J SEX MARITAL THER, V23, P165
  • [6] ASHTON AK, 1994, AM J PSYCHIAT, V151, P9
  • [7] EFFECT OF 3 WEEKS TREATMENT WITH YOHIMBINE ON SALIVARY SECRETION IN HEALTHY-VOLUNTEERS AND IN DEPRESSED-PATIENTS TREATED WITH TRICYCLIC ANTIDEPRESSANTS
    BAGHERI, H
    SCHMITT, L
    BERLAN, M
    MONTASTRUC, JL
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1992, 34 (06) : 555 - 558
  • [8] IS YOHIMBINE-INDUCED INCREASE IN SALIVARY SECRETION A KININ-DEPENDENT MECHANISM
    BAGHERI, H
    BOMPART, G
    GIROLAMI, JP
    MONTASTRUC, JL
    MONTASTRUC, P
    [J]. FUNDAMENTAL & CLINICAL PHARMACOLOGY, 1992, 6 (01) : 17 - 20
  • [9] A comparative study of the effects of yohimbine and anetholtrithione on salivary secretion in depressed patients treated with psychotropic drugs
    Bagheri, H
    Schmitt, L
    Berlan, M
    Montastruc, JL
    [J]. EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1997, 52 (05) : 339 - 342
  • [10] EVIDENCE FOR ACTIVATION OF BOTH ADRENERGIC AND CHOLINERGIC NERVOUS PATHWAYS BY YOHIMBINE, AN ALPHA(2)-ADRENOCEPTOR ANTAGONIST
    BAGHERI, H
    CHALE, JJ
    GUYEN, LN
    TRAN, MA
    BERLAN, M
    MONTASTRUC, JL
    [J]. FUNDAMENTAL & CLINICAL PHARMACOLOGY, 1995, 9 (03) : 248 - 254