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Journal of herbal pharmacotherapy最新文献

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Colon Cleansing 清肠
Pub Date : 2006-01-01 DOI: 10.1080/J157v06n02_08
Steven Horne
Intestinal inflammation and leaky gut syndrome can be at the root of many health problems. Colon cleansing is a popular therapy among alternative practitioners, but many myths surround it. The scientifically inaccurate way many traditional healers try to explain therapeutic mechanisms is one of the obstacles that inhibits dialog between traditional healers and practitioners of modern medicine. The therapy actually has clinical value, but the explanations used to promote the therapies are the stuff of herbal legends, not scientific fact. The concept of cleansing is actually a metaphorical explanation for a therapy that improves detoxification via the liver and gastrointestinal tract and reduces inflammation or irritation to mucous membranes of the GI tract.
肠道炎症和漏肠综合征可能是许多健康问题的根源。结肠清洗是一种很流行的治疗方法,但围绕它有很多误解。许多传统治疗师试图解释治疗机制的方式在科学上是不准确的,这是阻碍传统治疗师和现代医学从业者之间对话的障碍之一。这种疗法实际上具有临床价值,但用于推广这种疗法的解释是草药传说,而不是科学事实。清洁的概念实际上是对一种疗法的隐喻性解释,这种疗法通过肝脏和胃肠道改善排毒,减少对胃肠道粘膜的炎症或刺激。
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引用次数: 14
Peppermint (Mentha Xpiperita) 薄荷(薄荷味)
Pub Date : 2006-01-01 DOI: 10.1080/J157v07n02_07
Thomas Brendler, Joerg Gruenwald, Catherine Ulbricht, Ethan Basch
An evidence-based systematic review including written and statistical analysis of scientific literature, expert opinion, folkloric precedent, history, pharmacology, kinetics/dynamics, interactions, adverse effects, toxicology and dosing.
以证据为基础的系统评价,包括对科学文献、专家意见、民间先例、历史、药理学、动力学/动力学、相互作用、不良反应、毒理学和剂量的书面和统计分析。
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引用次数: 1
Protective effect of Indigofera aspalathoides against CCl4-induced hepatic damage in rats. 板蓝草对ccl4致大鼠肝损伤的保护作用。
Pub Date : 2006-01-01
B Rajkapoor, B Jayakar, S Kavimani, N Murugesh

The alcoholic extract of stem of Indigofera aspalathoides was evaluated for its antihepatotoxic activity against CCl(4)-induced hepatic damage in rats. The activity was evaluated by using biochemical parameters, such as serum glutamate pyruvate transaminase (SGPT), serum glutamate oxaloacetate transaminase (SGOT), alkaline phosphatase (ALP), total bilirubin and gama glutamate transpeptidase (GGTP). The histopathological changes of liver sample were compared with respective control. The extract showed remarkable hepatoprotective effect.

研究了蓝草茎醇提物对CCl(4)致大鼠肝损伤的抗肝毒活性。采用血清谷氨酸丙酮转氨酶(SGPT)、谷氨酸草酰乙酸转氨酶(SGOT)、碱性磷酸酶(ALP)、总胆红素和γ谷氨酸转肽酶(GGTP)等生化指标评价其活性。将肝组织病理变化与对照组进行比较。该提取物具有显著的保肝作用。
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引用次数: 0
Cardiac activity of isolated constituents of Inula racemosa. 总状菊分离成分的心脏活性研究。
Pub Date : 2006-01-01 DOI: 10.1080/j157v06n03_03
P D Lokhande, B S Dhaware, S C Jagdale, A R Chabukswar, S A Mulkalwar

Roots of the plant Inula racemosa are used as folk medicine in east Asia and Europe. Inula racemosa in combination with Commiphora mukul was reported to cure myocardial ischemia. However, systematic investigation of the plant for its specific role in heart diseases has not been conducted so far. In the present study, we have reported the isolation of four major constituents A, B, C and D along with some minor constituents from the plant Inula racemosa. Among the major constituent, constituent Dhas been selected first from spectral data and studied for its cardiac activity on isolated frog heart. The experimental data show that constituent D decreases heart rate and force of contraction at 40 mcg/ml. Actions of Adrenaline are blocked by constituent D and it also acts as an agonist for Propranolol. The studies indicate that constituent D produces a negative ionotropic and negative chronotropic effect on frog's heart. These studies can be utilized as a cardiac marker for exploring the cardiac activity of the plant Inula racemosa.

总状菊的根在东亚和欧洲被用作民间药物。有报道称,总状菊与麻瓜合用可治疗心肌缺血。然而,到目前为止,还没有对这种植物在心脏病中的具体作用进行系统的调查。在本研究中,我们报道了从总状菊中分离到四种主要成分A、B、C和D以及一些次要成分。在主要成分中,首先从光谱数据中选择组分d,对其在离体青蛙心脏上的心脏活性进行了研究。实验数据表明,在40 mcg/ml时,成分D能降低心率和收缩力。肾上腺素的作用被成分D阻断,它也作为心得安的激动剂。研究表明,D成分对青蛙心脏具有负离子性和负变时性作用。这些研究结果可作为研究总状菊心脏活动的心脏标志物。
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引用次数: 20
The Neuropharmacology of L-Theanine(N-Ethyl-L-Glutamine) l-茶氨酸(n -乙基- l-谷氨酰胺)的神经药理学
Pub Date : 2006-01-01 DOI: 10.1080/J157v06n02_02
P. Nathan, Kristy Lu, M. Gray, C. Oliver
L-theanine (N-ethyl-L-glutamine) or theanine is a major amino acid uniquely found in green tea. L-theanine has been historically reported as a relaxing agent, prompting scientific research on its pharmacology. Animal neurochemistry studies suggest that L-theanine increases brain serotonin, dopamine, GABA levels and has micromolar affinities for AMPA, Kainate and NMDA receptors. In addition has been shown to exert neuroprotective effects in animal models possibly through its antagonistic effects on group 1 metabotrophic glutamate receptors. Behavioural studies in animals suggest improvement in learning and memory. Overall, L-theanine displays a neuropharmacology suggestive of a possible neuroprotective and cognitive enhancing agent and warrants further investigation in animals and humans.
l-茶氨酸(n -乙基- l-谷氨酰胺)或茶氨酸是绿茶中唯一发现的主要氨基酸。l -茶氨酸历来被报道为一种放松剂,促使人们对其药理学进行科学研究。动物神经化学研究表明,l -茶氨酸增加脑血清素、多巴胺、GABA水平,并对AMPA、Kainate和NMDA受体具有微摩尔亲和力。此外,在动物模型中已被证明可能通过其对1组代谢谷氨酸受体的拮抗作用发挥神经保护作用。对动物的行为研究表明,学习和记忆能力有所提高。总的来说,l -茶氨酸显示出一种神经药理学暗示,可能是一种神经保护和认知增强剂,值得在动物和人类中进一步研究。
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引用次数: 81
The neuropharmacology of L-theanine(N-ethyl-L-glutamine): a possible neuroprotective and cognitive enhancing agent. l-茶氨酸(n -乙基- l-谷氨酰胺)的神经药理学:一种可能的神经保护和认知增强剂。
Pub Date : 2006-01-01 DOI: 10.1300/J157V06N02_02
P. Nathan, Kristy Lu, M. Gray, C. Oliver
L-theanine (N-ethyl-L-glutamine) or theanine is a major amino acid uniquely found in green tea. L-theanine has been historically reported as a relaxing agent, prompting scientific research on its pharmacology. Animal neurochemistry studies suggest that L-theanine increases brain serotonin, dopamine, GABA levels and has micromolar affinities for AMPA, Kainate and NMDA receptors. In addition has been shown to exert neuroprotective effects in animal models possibly through its antagonistic effects on group 1 metabotrophic glutamate receptors. Behavioural studies in animals suggest improvement in learning and memory. Overall, L-theanine displays a neuropharmacology suggestive of a possible neuroprotective and cognitive enhancing agent and warrants further investigation in animals and humans.
l-茶氨酸(n -乙基- l-谷氨酰胺)或茶氨酸是绿茶中唯一发现的主要氨基酸。l -茶氨酸历来被报道为一种放松剂,促使人们对其药理学进行科学研究。动物神经化学研究表明,l -茶氨酸增加脑血清素、多巴胺、GABA水平,并对AMPA、Kainate和NMDA受体具有微摩尔亲和力。此外,在动物模型中已被证明可能通过其对1组代谢谷氨酸受体的拮抗作用发挥神经保护作用。对动物的行为研究表明,学习和记忆能力有所提高。总的来说,l -茶氨酸显示出一种神经药理学暗示,可能是一种神经保护和认知增强剂,值得在动物和人类中进一步研究。
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引用次数: 142
Devil's Claw (Harpagophytum procumbens DC): an evidence-based systematic review by the Natural Standard Research Collaboration. 魔鬼之爪(Harpagophytum procumbens DC):自然标准研究合作组织的循证系统综述。
Pub Date : 2006-01-01
Thomas Brendler, Joerg Gruenwald, Catherine Ulbricht, Ethan Basch

An evidence-based systematic review including written and statistical analysis of scientific literature, expert opinion, folkloric precedent, history, pharmacology, kinetics/dynamics, interaction, adverse effects, toxicology, and dosing.

以证据为基础的系统评价,包括对科学文献、专家意见、民间先例、历史、药理学、动力学/动力学、相互作用、不良反应、毒理学和剂量的书面和统计分析。
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引用次数: 0
Clinical Evaluation to Assess the Safety and Efficacy of Coded Herbal Medicine “Dysmo-off” versus Allopathic Medicine “Diclofenac Sodium” for the Treatment of Primary Dysmenorrhea 编码草药“dysmooff”与对抗性药物“双氯芬酸钠”治疗原发性痛经的安全性和有效性的临床评价
Pub Date : 2006-01-01 DOI: 10.1080/J157v06n01_03
Halima Nazar, K. Usmanghani
The purpose of the present research work was to carry out clinical study on primary dysmenorrhea to comparatively examine the coded herbal drug formulation “Dysmo-off” with authentic allopathic medicine “Diclofenac sodium” (NSAIDs). A random controlled clinical trial was conducted to compare the efficacy and safety of coded herbal medicinal treatments Dysmo-off with Diclofenac sodium/Phenylacetic acid. These evaluations were based on verbal rating scale so as to ascertain the rate of analgesic effects on dysmenorrhoeic pain. The patients were randomly allocated with the ratio of 1:2 for controlled treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) (n = 40) received Diclofenac sodium tablets twice daily for 4 days (50 mg one day prior to and three days after the menstruation), and test treatment with Dysmo-off (n = 80) received powdered Dysmo-off twice daily for four days (5 g one day prior to and three days after the menstruation). Treatment lasted for 4 consecutive menstrual cycles. Hemoglobin, ESR and ultrasound were measured at baseline during study. All subjects were clinically studied and completed the assigned therapy during the period May 2001 to June 2004.
本研究的目的是开展原发性痛经的临床研究,对编码的中药配方“dysmooff”与正品对抗性药物“双氯芬酸钠”(NSAIDs)进行对比检验。采用随机对照临床试验比较编码草药治疗dysmooff与双氯芬酸钠/苯乙酸的疗效和安全性。这些评价是基于口头评定量表,以确定镇痛效果对痛经疼痛的比率。随机按1:2的比例分配给非甾体抗炎药(NSAIDs)对照治疗组(n = 40),给予双氯芬酸钠片每日2次,连续4天(月经前1天、月经后3天各50 mg);给予dysmooff试验组(n = 80),给予dysmooff粉状,每日2次,连续4天(月经前1天、月经后3天各5 g)。治疗持续4个月经周期。在研究期间测量血红蛋白、血沉和超声。所有受试者在2001年5月至2004年6月期间进行临床研究并完成指定的治疗。
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引用次数: 8
Clinical evaluation to assess the safety and efficacy of coded herbal medicine "Dysmo-off" versus allopathic medicine "Diclofenac sodium" for the treatment of primary dysmenorrhea. 临床评价编码草药“dysmooff”与对抗疗法药物“双氯芬酸钠”治疗原发性痛经的安全性和有效性。
Pub Date : 2006-01-01
Halima Nazar, Khan Usmanghani

The purpose of the present research work was to carry out clinical study on primary dysmenorrhea to comparatively examine the coded herbal drug formulation "Dysmo-off" with authentic allopathic medicine "Diclofenac sodium" (NSAIDs). A random controlled clinical trial was conducted to compare the efficacy and safety of coded herbal medicinal treatments Dysmo-off with Diclofenac sodium/Phenylacetic acid. These evaluations were based on verbal rating scale so as to ascertain the rate of analgesic effects on dysmenorrhoeic pain. The patients were randomly allocated with the ratio of 1:2 for controlled treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) (n = 40) received Diclofenac sodium tablets twice daily for 4 days (50 mg one day prior to and three days after the menstruation), and test treatment with Dysmo-off (n = 80) received powdered Dysmo-off twice daily for four days (5 g one day prior to and three days after the menstruation). Treatment lasted for 4 consecutive menstrual cycles. Hemoglobin, ESR and ultrasound were measured at baseline during study. All subjects were clinically studied and completed the assigned therapy during the period May 2001 to June 2004.

本研究的目的是开展原发性痛经的临床研究,对编码的中药配方“dysmooff”与正品对抗性药物“双氯芬酸钠”(NSAIDs)进行对比检验。采用随机对照临床试验比较编码草药治疗dysmooff与双氯芬酸钠/苯乙酸的疗效和安全性。这些评价是基于口头评定量表,以确定镇痛效果对痛经疼痛的比率。随机按1:2的比例分配给非甾体抗炎药(NSAIDs)对照治疗组(n = 40),给予双氯芬酸钠片每日2次,连续4天(月经前1天、月经后3天各50 mg);给予dysmooff试验组(n = 80),给予dysmooff粉状,每日2次,连续4天(月经前1天、月经后3天各5 g)。治疗持续4个月经周期。在研究期间测量血红蛋白、血沉和超声。所有受试者在2001年5月至2004年6月期间进行临床研究并完成指定的治疗。
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引用次数: 0
Frequently asked questions (FAQ). 常见问题(FAQ)。
Pub Date : 2006-01-01
K P Khalsa

As Americans use botanical medicines in ever-increasing numbers, they are moving beyond capsules and tinctures, and turning to assorted preparations that will complete their herbal medicine chest. According to The Arthritis Foundation, almost 45% of patients apply ointments or rubs for osteoarthritis. Topical preparations have a long history in traditional herbal medicine systems, and make up a significant proportion of the armamentarium of indigenous practitioners. Although contemporary patients are often resistant to the inconvenience of topical preparations, they often will become compliant after a notable success. The nomenclature of these topical preparations, as one would expect, is murky. There are no clear and consistent definitions for the assorted terms, and different sources will use different terms for the same material or process.

随着美国人越来越多地使用植物药物,他们正在超越胶囊和酊剂,转向各种制剂,以完善他们的草药库。根据关节炎基金会的数据,近45%的患者使用软膏或按摩治疗骨关节炎。局部制剂在传统草药系统中具有悠久的历史,并且在土著从业者的装备中占很大比例。虽然当代患者往往对局部制剂的不便有抵抗力,但在取得显著成功后,他们往往会变得顺从。正如人们所预料的那样,这些局部制剂的命名是模糊的。对于分类的术语没有明确和一致的定义,不同的来源将对相同的材料或过程使用不同的术语。
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引用次数: 0
期刊
Journal of herbal pharmacotherapy
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