Jordan Jens, Shannon John R, Diedrich André, Black Bonnie, Robertson David, Biaggioni Italo
Department of Medicine and Pharmacology, Vanderbilt University, Nashville, Tenn 37212, USA.
Circulation. 2004 Apr 20;109(15):1823-5. doi: 10.1161/01.CIR.0000126283.99195.37. Epub 2004 Apr 5.
The use of ephedra alkaloids in over-the-counter preparations has been associated with potentially serious cerebrovascular events. Because of its potential association with hemorrhagic strokes, phenylpropanolamine has been largely substituted for by pseudoephedrine, but it is not clear whether this is indeed a safer alternative. It would be important to understand the cardiovascular effects of ephedra alkaloids, but these are normally masked by baroreflex buffering mechanisms. We therefore investigated the effects of ephedra alkaloids in patients with autonomic impairment and explored their potential interaction with water ingestion.
The cardiovascular effects of phenylpropanolamine or pseudoephedrine, alone and in combination with water, were determined in 13 subjects with impairment of baroreflex function due to autonomic failure. Phenylpropanolamine, 12.5 to 25 mg PO, increased systolic blood pressure (SBP) by 21+/-14 mm Hg after 90 minutes. However, when ingested with 16 oz of room temperature tap water, phenylpropanolamine increased SBP by 82+/-2 mm Hg. Pseudoephedrine, 30 mg PO, increased SBP on average 52+/-9 mm Hg when taken with 16 oz of water and by as much as 88 mm Hg.
Ephedra alkaloids increase blood pressure significantly in individuals with impaired baroreflex function. Concomitant ingestion of ephedra alkaloids and water produced a greater increase in blood pressure. If used cautiously, this interaction can be beneficial in the treatment of orthostatic hypotension. On the other hand, it could contribute to the cardiovascular complications associated with the use of ephedra alkaloids, given that baroreflex function varies widely in normal individuals and is impaired in several medical conditions.
非处方制剂中麻黄生物碱的使用与潜在的严重脑血管事件有关。由于其与出血性中风的潜在关联,苯丙醇胺已在很大程度上被伪麻黄碱所取代,但尚不清楚这是否真的是一种更安全的替代品。了解麻黄生物碱的心血管效应很重要,但这些效应通常会被压力反射缓冲机制所掩盖。因此,我们研究了麻黄生物碱对自主神经功能受损患者的影响,并探讨了它们与饮水之间的潜在相互作用。
在13名因自主神经功能衰竭导致压力反射功能受损的受试者中,测定了苯丙醇胺或伪麻黄碱单独使用以及与水联合使用时的心血管效应。口服12.5至25毫克苯丙醇胺后,90分钟时收缩压(SBP)升高21±14毫米汞柱。然而,当与16盎司室温自来水一起摄入时,苯丙醇胺使收缩压升高82±2毫米汞柱。口服30毫克伪麻黄碱,与16盎司水一起服用时,平均使收缩压升高52±9毫米汞柱,最高可达88毫米汞柱。
麻黄生物碱在压力反射功能受损的个体中会显著升高血压。同时摄入麻黄生物碱和水会使血压升高幅度更大。如果谨慎使用,这种相互作用在治疗体位性低血压方面可能有益。另一方面,鉴于正常个体的压力反射功能差异很大,且在几种疾病中会受损,这可能会导致与使用麻黄生物碱相关的心血管并发症。