Role of noradrenergic and dopaminergic systems in the antinociceptive effect of N-(3-(phenylselanyl)prop-2-yn-1-yl)benzamide in mice.

Pain has a negative impact on public health, reducing quality of life. Unfortunately, current treatments are not fully effective and have adverse effects. Therefore, there is a need to develop new analgesic compounds. Due to promising results regarding the antinociceptive effect of N-(3-(phenylselanyl)prop-2-in-1-yl)benzamide (SePB), this study aimed to evaluate the participation of the dopaminergic and noradrenergic systems in this effect in mice, as well as its toxicity. To this, the antagonists sulpiride (D2/D3 receptor antagonist, 5 mg/kg), SCH-23390 (D1 receptor antagonist, 0.05 mg/kg), prazosin (α1 adrenergic receptor antagonist, 0.15 mg/kg), yohimbine (α2-adrenergic receptors, 0.15 mg/kg) and propranolol (non-selective ß-adrenergic antagonist, 10 mg/kg) were administered intraperitoneally to mice 15 min before SePB (10 mg/kg, intragastrically), except for propranolol (20 min). After 26 min of SePB administration, the open field test was performed for 4 min to assess locomotor activity, followed by the tail immersion test to measure the nociceptive response. For the toxicity test, animals received a high dose of 300 mg/kg of SePB. SePB showed an increase in the latency for nociceptive response in the tail immersion test, and this effect was prevented by SCH-23390, yohimbine and propranolol, indicating the involvement of D1, α2 and ß-adrenergic receptors in the antinociceptive mechanism of the SePB effect. No changes were observed in the open field test, and the toxicity assessment suggested that SePB has low potential to induce toxicity. These findings contribute to understanding SePB's mechanism of action, with a focus on the development of new alternatives for pain treatment.

Efeitos cardiovasculares da medetomidina e cetamina em Puma concolor e tempo de recuperação após aplicação de ioimbina ou atipamezole / [Cardiovascular effects of medetomidine and cetamine in Puma concolor and recovery time after application of ioimbin or atipamezole]

O objetivo deste estudo foi avaliar as alterações cardiorrespiratórias causadas pela medetomidina associada à cetamina, e o tempo de recuperação após aplicação intramuscular de atipamezole ou ioimbina em Puma concolor. Para isso, foi realizada a aplicação de medetomidina (100µg/kg) associada à cetamina (5mg/kg) em 11 onças-pardas, sendo os parâmetros cardiorrespiratórios registrados a cada 15 minutos, durante 90 minutos de avaliação. Em seguida, a anestesia foi revertida com aplicação intramuscular de ioimbina (0,4mg/kg; n=5) ou atipamezole (0,25mg/kg; n=6), sendo analisado o tempo até a recuperação. Dos parâmetros cardiorrespiratórios avaliados, houve diferença apenas na frequência respiratória (entre os momentos 60 e 90 minutos), estando esta, todavia, dentro do intervalo de referência para a espécie. Além disso, verificou-se tempo para decúbito esternal significativamente menor nos animais do grupo atipamezole (18±7 minutos), quando comparado ao grupo ioimbina (36±17 minutos), entretanto o tempo de recuperação completa foi estatisticamente igual entre os dois reversores analisados. Assim, a associação anestésica promoveu anestesia eficiente, segura e de rápida indução em onças-pardas, permitindo a imobilização dos animais durante os 90 minutos de avaliação, sem a ocorrência de complicações. Ao se comparar a reversão anestésica com atipamezole e ioimbina, observou-se equivalência dos fármacos no tempo de recuperação completa dos animais.(AU)

The aim of this study was to evaluate the cardiorespiratory changes caused by ketamine-associated medetomidine, and the recovery time after intramuscular application of atipamezole or yohimbine in Puma concolor. For this, the application of medetomidine (100µg/kg) associated with ketamine (5mg/kg) was performed in eleven brown ounces, and the cardiorespiratory parameters were recorded every 15 minutes during 90 minutes of evaluation. Afterwards, anesthesia was reversed with intramuscular application of yohimbine (0.4mg/kg; n=5) or atipamezole (0.25mg/kg; n=6), and time to recovery was analyzed. Of the cardiorespiratory parameters evaluated, there was a difference only in respiratory rate (between 60 and 90 minutes), however, within the reference range for the species. In addition, there was a significantly shorter time for sternal decubitus in the animals of the atipamezole group (18±7 minutes) when compared to the yohimbine group (36±17 minutes), however the complete recovery time was statistically equal between the two reversers analyzed. Thus, the anesthetic association promoted efficient, safe and fast induction anesthesia in puma, allowing the animals to be immobilized during the 90 minutes of evaluation without complications. Comparing anesthetic reversal with atipamezole and yohimbine, drug equivalence was observed in the complete recovery time of the animals.(AU)

Anti-hyperalgesic effect of Lippia grata leaf essential oil complexed with ß-cyclodextrin in a chronic musculoskeletal pain animal model: Complemented with a molecular docking and antioxidant screening.

BACKGROUND: Due to its unclear pathophysiology, the pharmacological treatment of fibromyalgia is a challenge for researchers. Studies using medicinal plants, such as those from the genus Lippia, complexed with cyclodextrins (CDs) have shown innovative results. OBJECTIVE: The present research intended to evaluate the effect of an inclusion complex containing ß-cyclodextrin (ßCD) inclusion complex with Lippia grata (LG) essential oil in a chronic musculoskeletal pain model, its central activity and its possible interaction with neurotransmitters involved in pain. METHODS: After acid saline-induced chronic muscle pain, male mice were evaluated for primary and secondary hyperalgesia and muscle strength. Moreover, an antagonist assay was performed to assess the possible involvement of the opioidergic, serotonergic and noradrenergic pathways. In addition, Fos protein in the spinal cord was assessed, and a docking study and antioxidant assays were performed. RESULTS: The treatment with LG-ßCD, especially in the dose of 24mg/kg, was able to significantly decrease (p<0.05) the paw withdrawal and muscle threshold. Furthermore, LG-ßCD was shown to affect the opioidergic and serotonergic pathways. There were no significant changes in muscle strength. Fos protein immunofluorescence showed a significant decrease in expression in the dorsal horn of the spinal cord. The main compounds of LG showed through the docking study interaction energies with the alpha-adrenergic and µOpioid receptors. In all antioxidant assays, LG exhibited stronger antioxidant activities than LG-ßCD. CONCLUSION: This study suggested that LG-ßCD could be considered as a valuable source for designing new drugs in the treatment of chronic pain, especially musculoskeletal pain.

Gastroprotective and ulcer healing effects of hydroethanolic extract of leaves of Caryocar coriaceum: Mechanisms involved in the gastroprotective activity.

This work aimed to determine the chemical fingerprint of hydroethanolic extract of leaves of Caryocar coriaceum (HELCC) and the gastroprotective activity. The chemical fingerprint of HELCC was analyzed by HPLC-DAD, to quantify total phenols and flavonoids were carried out by Folin-Ciocalteu reagent and aluminum chloride assay, while in vitro antioxidant activity was evaluated by the DPPH method. The methods used to determine pharmacological activity were: gastroprotective screening test in classical models of induced acute and chronic gastric lesions and physical barrier test. Further assays were performed to demonstrate the involvement of NO, prostaglandins, ATP-dependent potassium channels, TRPV, noradrenergic α2 receptors, histamines, and opioids. The DPPH method demonstrated the antioxidant activity of the extract, in vitro, explained by the presence of polyphenols and flavonoids. Oral administration of the extract, previously dissolved in deionized water, at a dose of 100 mg/kg decreased the lesions induced by indomethacin, acidified ethanol, ethanol and acetic acid by 75.0, 72.8, 69.4 and 86.2% respectively. It was demonstrated that opioid receptors, α2-adrenergic receptors and primary afferent neurons sensitive to capsaicin were involved in the mechanism of gastric protection, in addition to the contribution of NO and prostaglandins. The results show that extract is a promising candidate for the treatment of gastric ulcers.

Evaluation of the noradrenergic pathway and alpha-2 and beta-receptors in the modulation of the analgesia induced by transcutaneous electric nerve stimulation of high and low frequencies / Evaluación de la vía noradrenérgica y de los receptores alfa-2 y beta en la modulación de analgesia inducida por la estimulación eléctrica nerviosa transcutánea con alta y baja frecuencia / Avaliação da via noradrenérgica e dos receptores alfa-2 e beta na modulação da analgesia induzida pela estimulação elétrica nervosa transcutânea de alta e de baixa frequência

Transcutaneous electric nerve stimulation is a noninvasive method used in clinical Physiotherapy to control acute or chronic pain. Different theories have been proposed to explain the mechanism of the analgesic action of transcutaneous electric nerve stimulation, as the participation of central and peripheral neurotransmitters. The aim of this study was to evaluate the involvement of noradrenergic pathway and of the receptors alfa-2 and beta in the modulation of analgesia produced by transcutaneous electric nerve stimulation of high and low frequency in Wistar rats after chronic treatment with propranolol or yohimbine intraperitoneally. Animals weighing 200 to 300 g were divided into 9 groups (n=8), which were obtained nociceptive thresholds through the Tail Flick before and after application of TENS for comparing the change of pain. The administration of yohimbine or propranolol at a dose of 3 mg/kg was effective in antagonizing the analgesia induced by high (150 Hz) and low (10 Hz) frequency transcutaneous electric nerve stimulation according to ANOVA test followed by Duncan post hoc test (p<0.05). Thus, it is suggested the involvement of alpha-2 and beta noradrenergic receptors in the modulation of transcutaneous electric nerve stimulation-induced analgesia.

La estimulación eléctrica nerviosa transcutánea es un método no invasivo utilizado en la clínica de Fisioterapia para controlar el dolor agudo y crónico. Diversas teorías son propuestas para explanar el mecanismo de acción analgésico de la estimulación eléctrica nerviosa transcutánea, como la participación de neurotransmisores centrales y periféricos. El objetivo del presente estudio fue evaluar la participación de la vía noradrenérgica y de los receptores alfa-2 y beta en la modulación de analgesia inducida por la estimulación eléctrica nerviosa transcutánea con alta y baja frecuencia en ratos del tipo Wistar, después del tratamiento crónico con yohimbina o propranolol por la vía intraperitoneal. Animales que pesaban 200 y 300 g fueron divididos en nueve grupos (n=8), por los cuales fueron obtenidos los umbrales nociceptivos por medio del Tail Flick, antes y después de la aplicación de la estimulación eléctrica nerviosa transcutánea con el intuito de comparar la alteración del cuadro álgico. La administración de yohimbina o propranolol en el dosis de 3 mg/kg fue eficaz en resultar en una antagonización de analgesia inducida por la estimulación eléctrica nerviosa transcutánea con alta (150 Hz) y baja (10 Hz) frecuencia, de acuerdo al test de ANOVA seguido del test post-hoc de Duncan (p>0,05). Por lo tanto, se sugiere el envolvimiento de los receptores noradrenergicos alfa-2 y beta en la modulación de analgesia inducida por la estimulación eléctrica nerviosa transcutánea.

Estimulação elétrica nervosa transcutânea é um método não invasivo utilizado na clínica de Fisioterapia para controlar dores aguda ou crônica. Diferentes teorias são propostas para explicar o mecanismo de ação analgésica da estimulação elétrica nervosa transcutânea, como a participação de neurotransmissores centrais e periféricos. O objetivo do presente estudo foi avaliar a participação da via noradrenérgica e dos receptores alfa-2 e beta na modulação da analgesia induzida pela estimulação elétrica nervosa transcutânea de alta e baixa frequência em ratos Wistar, após tratamento crônico com ioimbina ou propranolol por via intraperitoneal. Animais pesando entre 200 e 300 g foram divididos em 9 grupos (n=8), dos quais se obteve os limiares nociceptivos por meio do Tail Flick antes e após a aplicação da estimulação elétrica nervosa transcutânea para comparação de mudança do quadro álgico. A administração de ioimbina ou de propranolol na dose de 3 mg/kg foi efetiva em causar uma antagonização da analgesia induzida pela estimulação elétrica nervosa transcutânea de alta (150 Hz) e baixa frequência (10 Hz) segundo teste ANOVA seguido do teste post hoc Duncan (p<0,05). Dessa forma, sugere-se o envolvimento de receptores noradrenérgicos alfa-2 e beta na modulação da analgesia induzida pela estimulação elétrica nervosa transcutânea. .

Paradoxical effect of noradrenaline-mediated neurotransmission in the antinociceptive phenomenon that accompanies tonic-clonic seizures: role of locus coeruleus neurons and α(2)- and ß-noradrenergic receptors.

The postictal state is generally followed by antinociception. It is known that connections between the dorsal raphe nucleus, the periaqueductal gray matter, and the locus coeruleus, an important noradrenergic brainstem nucleus, are involved in the descending control of ascending nociceptive pathways. The aim of the present study was to determine whether noradrenergic mechanisms in the locus coeruleus are involved in postictal antinociception. Yohimbine (an α(2)-receptor antagonist) or propranolol (a ß-receptor antagonist) was microinjected unilaterally into the locus coeruleus, followed by intraperitoneal administration of pentylenetetrazole (PTZ), a noncompetitive antagonist that blocks GABA-mediated Cl(-) influx. Although the administration of both yohimbine and propranolol to the locus coeruleus/subcoeruleus area resulted in a significant decrease in tonic or tonic-clonic seizure-induced antinociception, the effect of yohimbine restricted to the locus coeruleus was more distinct compared with that of propranolol, possibly because of the presynaptic localization of α(2)-noradrenergic receptors in locus coeruleus neurons. These effects were related to the modulation of noradrenergic activity in the locus coeruleus. Interestingly, microinjections of noradrenaline into the locus coeruleus also decrease the postictal antinociception. The present results suggest that the mechanism underlying postictal antinociception involves both α(2)- and ß-noradrenergic receptors in the locus coeruleus, although the action of noradrenaline on these receptors causes a paradoxical effect, depending on the nature of the local neurotransmission.

Efeitos hemogasométricos da xilazina e da romifidina em cabras tratadas por ioimbina / Haemogasometric effects of xylazine and romifidine in goats treated with yohimbine

Estudaram-se as alterações produzidas por doses equipotentes de xilazina e romifidina e os efeitos da administração subseqüente de ioimbina em oito cabras mestiças. Respeitou-se um intervalo de sete dias entre os seguintes tratamentos: A- 250µg/kg/IM de xilazina e 0,1ml/kg/IV de solução fisiológica, B- 250µg/kg/IM de xilazina e 250µg/kg/IV de ioimbina, C- 25µg/kg/IM de romifidina e 0,1ml/kg/IV de solução fisiológica, D- 25µg/kg/IM de romifidina e 250µg/kg/IV de ioimbina. Foram mensurados a freqüência respiratória, o pH, as pressões parciais de oxigênio e dióxido de carbono, a concentração de íon bicarbonato, o excesso de bases e a saturação de oxigênio no sangue arterial. Utilizou-se um delineamento experimental crossover, e as médias foram comparadas pelo teste Duncan (Pmenor ou igual a 0,05). Xilazina e romifidina reduziram a pressão arterial de oxigênio e aumentaram a pressão arterial de dióxido de carbono. A ioimbina reverteu os efeitos da xilazina e da romifidina sobre as pressões parciais de oxigênio e dióxido de carbono no sangue arterial.

Efeitos hemogasométricos da xilazina e da romifidina em cabras tratadas por ioimbina / Haemogasometric effects of xylazine and romifidine in goats treated with yohimbine

Estudaram-se as alterações produzidas por doses equipotentes de xilazina e romifidina e os efeitos da administração subseqüente de ioimbina em oito cabras mestiças. Respeitou-se um intervalo de sete dias entre os seguintes tratamentos: A- 250µg/kg/IM de xilazina e 0,1ml/kg/IV de solução fisiológica, B- 250µg/kg/IM de xilazina e 250µg/kg/IV de ioimbina, C- 25µg/kg/IM de romifidina e 0,1ml/kg/IV de solução fisiológica, D- 25µg/kg/IM de romifidina e 250µg/kg/IV de ioimbina. Foram mensurados a freqüência respiratória, o pH, as pressões parciais de oxigênio e dióxido de carbono, a concentração de íon bicarbonato, o excesso de bases e a saturação de oxigênio no sangue arterial. Utilizou-se um delineamento experimental crossover, e as médias foram comparadas pelo teste Duncan (Pd<0,05). Xilazina e romifidina reduziram a pressão parcial de oxigênio e aumentaram a pressão parcial de dióxido de carbono. A ioimbina reverteu os efeitos da xilazina e da romifidina sobre as pressões parciais de oxigênio e dióxido de carbono no sangue arterial.(AU)

With the purpose to assess some of the clinical and laboratorial features induced by xylazine and romifidine, at equipotent sedative doses, followed by the use of yohimbine, eight crossbred female goats were assigned randomly to four treatments at the following dose rates: A- 250µg/kg/IM xylazine plus 0.1ml/kg/IV saline solution, B- 250µg/kg/IM xylazine plus 250µg/kg/IV de yohimbine, C- 25µg/kg/IM romifidine plus 0.1ml/kg/IV saline, D- 25µg/kg/IM romifidine plus 250µg/kg/IV yohimbine. Breath rate, pH, oxygen and carbon dioxide tensions, concentration of hydrogen carbonate, base excess and fraction of oxyhemoglobin of arterial blood were measured. A crossover experimental design was used and the comparisons of treatment means were performed by Duncan test (Pd<0.05). Xylazine and romifidine induced a decrease in partial pressure of oxygen and an increase in partial pressure of carbon dioxide in arterial blood. Yohimbine reversed the effects of xylazine and romifidine on arterial oxygen carbon partial pressures.(AU)

The comparative efficacy of yohimbine and atipamezole to treat amitraz intoxication in dogs.

This study compared the efficacy of yohimbine with atipamezole, a new alpha2 adrenergic antagonist, to treat canine amitraz intoxication. Thirty dogs were divided equally into 3 groups (A, AY, and AA). Group A received 2.5% amitraz iv at 1 mg/kg; Group AY received the same dose of amitraz followed 30 min later by 0.1 mg/kg (2 mg/mL) yohimbine iv; and Group AA received the same dose of amitraz followed 30 min later by 0.2 mg/kg (5 mg/ mL) atipamezole iv. Temperature, heart rate, respiratory frequency, mean arterial pressure, degree of sedation, mean time of tranquilization and diameter of pupils were monitored for 360 min. Sedation, loss of reflexes, hypothermia, bradycardia, hypotension, bradypnea and mydriasis were observed in Group A, with 3rd eyelid prolapse, increased diuresis and vomiting in some animals. Yohimbine reversed all alterations induced by amitraz, but induced significant cardiorespiratory effects such as tachycardia and tachypnea. Atipamezole was a useful antagonist for amitraz, with less cardiorespiratory effects, suggesting its potential role as an alternative treatment of amitraz intoxication in dogs.

Disfunción sexual eréctil en la diabetes mellitus / Sexual erectile dysfunction in diabetes melliltus

El objetivo de esta revisión es actualizar diferentes aspectos de la disfunción sexual eréctil (DSE) en el diabético: epidemiología, patogénesis, clínica, diagnóstico y tratamiento. Una de las principales causas de la DSE en todo el mundo lo constituye la diabetes mellitus (DM). Se calcula una prevalencia de DSE en la DM de hasta el 50 porciento (rango de 38 al 59 porciento). Se considera que la causa puede deberse principalmente a neuropatía y/o vasculopatía. La evaluación clínica inicial del diabético con DSE abarca: historia clínica completa que debe incluir, historia psicosocial y sexual. El diagnóstico se precisará con pruebas hemodinámicas y electrodiagnósticas: plestimografía, flujometría, drogas vasoactivas, biotensometría, reflejo bulbo cavernoso y potenciales evocados somatosensoriales. El tratamiento de la DSE en la DMI está dirigido a la obtención de un control metabólico optimizado y a la erradicación de los factores de riesgo modificables. Como tratamiento farmacológico se ha empleado la yohimbina (antagonista alfa-2 adrenérgico), isoxuprina (agonista beta-adrenérgico), trazadone (antidepresivo tricíclico con efectos colinérgicos limitados), citrato de sildenafil (inhibidor selectivo de la fosfodiesterasa del tipo 5). También se han utilizado diversos dispositivos que permiten inducir la erección asistida (vacum) y la inyección en los cuerpos cavernosos de sustancias vasoactivas (fentolamina, papaverina, y prostaglandina El). Los procederes quirúrgicos dependen de la causa e incluyen ligadura venosa y revacularización arterial. Cuando los métodos antes señalados fallan, está indicada la inserción de una prótesis peneana (inflables o no inflables). En la actualidad, el fármaco de elección para el tratamiento de la DSE es el citrato de sildenafil(AU)

This review is aimed at bringing up-to-date different aspects of sexual erectile dysfunction (SED) in the diabetic patient: epidemiology, pathogenesis, clinic, diagnosis and treatment. Diabetes mellitus (DM) is one of the main causes of SED in the world. A prevalance of SED in DM of up to 50 percent (range from 38 to 59 percent) is calculated . It is considered that it is mainly caused by neuropathy and/or vasculopathy. The initial clinical evaluation of the diabetic patient with SED includes a complete medical history that should comprise psychosocial and sexual history. The diagnosis will be determined by hemodynamic and electrodiagnostic tests, phlethysmography, flowmetry, vasoactive drugs, biotensometry, bulbocavernous reflex and evoked somatosensorial potentials. The treatment of DSE in DM is directed to the obtention of an optimized metabolic control and to the erradication of the modifiable risk factors. Yohimbine (adrenergic alpha-2 antagonist), isoxuprine (beta-adrenergic agonist), trazadone (tricyclic antidepressive with limited cholinergic effects), and sildenafil (selective inhibitor of type 5 phosphodiesterase) have been used in the pharmacological treatment. Diverse devices allowing to induce the assisted erection (vacuum) and the injection in the corpus cavernous of vasoactive substances (phentolamine, papaverine and prostaglandin EI) have also been utilized. The surgical procedures depend on the cause and include venous ligation and arterial revascularization. When the above mentioned methods fail, the insertion of a penial prosthesis (inflatable or not) is indicated. At present, sildenafil is the elective drug to treat SED(AU)

Therapeutic effects of high dose yohimbine hydrochloride on organic erectile dysfunction.

PURPOSE: We evaluated men with organic erectile dysfunction treated with placebo and high dose oral yohimbine hydrochloride. MATERIALS AND METHODS: We selected 22 patients with organic erectile dysfunction (mean age 58 years) for treatment in the andrology outpatient clinic. These patients had been previously undergone neurological, vascular, hormonal and psychological testing, and were treated during an equal period of 30 days with placebo and daily single dose oral 100 mg. yohimbine. The response to treatment was evaluated via a questionnaire that comprised the outcome items of complete--normal penile rigidity enabling vaginal penetration, partial--erection improved but not sufficiently for appropriate vaginal penetration, none--no improvement and worse--erection deteriorated. The patients consented to treatment after being told of the severe adverse effects that might occur. RESULTS: The most common side effects were anxiety, increase in cardiac frequency, increased urinary output and headache but in no case was treatment discontinued. Of the patients 3 (13.6%) and 12 (54.5%) reported complete or partial response to treatment, respectively. However, statistical analysis disclosed no significant difference when yohimbine was compared to placebo (p < 0.05). CONCLUSIONS: Oral 100 mg. single dose daily yohimbine promotes no improvement in patients with organic erectile dysfunction.

Tratamiento farmacológico de la disfunción eréctil / Farmacologic treatment of the erectile disfunction

Anatomía funcional del pene.- Mecanismos que regulan la erección.- Disfunción sexual eréctil: Etiología, diagnóstico, tratamiento.- Medicación oral; Aplicación transepitelial de drogas vasoactivas; Tratamiento hormonal; Fármacotest; Inyección intracavernosa: complicaciones.- Disfunción sexual eréctil orgánica y psicógena con erección farmacológica.- Disfunción sexual eréctil en la diabetes y el tabaquismo

Tratamiento farmacológico de la disfunción eréctil / Farmacologic treatment of the erectile disfunction

Anatomía funcional del pene.- Mecanismos que regulan la erección.- Disfunción sexual eréctil: Etiología, diagnóstico, tratamiento.- Medicación oral; Aplicación transepitelial de drogas vasoactivas; Tratamiento hormonal; Fármacotest; Inyección intracavernosa: complicaciones.- Disfunción sexual eréctil orgánica y psicógena con erección farmacológica.- Disfunción sexual eréctil en la diabetes y el tabaquismo

Efeitos terapeuticos do hidroclorato de ioimbina na disfunçao sexual eretil / Therapeutic effects of the yohimbine hydrochloride in sexual erectile dysfunction

A ioimbina e uma alternativa disponivel para o tratamento da disfunçao eretil masculina, embora a avaliaçao isolada de seus efeitos terapeuticos tenha sido dificultada devido ao seu uso em composiçao com outros farmacos como a testosterona e a estricnina. Neste trabalho sao relatados os resultados obtidos no estudo prospectivo de vinte pacientes que receberam placebo e hidroclorato de ioimbina (HI) para o tratamento da disfunçao eretil de etiologia variada. Resposta positiva foi obtida em treze (65//) dos vinte pacientes que receberam HI 100 mg uma vez ao dia no periodo de um mes, o que nao e estatisticamentesignificativo quando comparado com aproximadamente 67//de respostas positivas com placebo (p>0,05). Efeitos adversos como ansiedade, taquicardia, cefaleia e aumento de frequencia urinaria foram os mais observados. Avaliaçoes semioticas e estudos controlados por periodo de tempo mais prolongado sao requeridos para que se faça uma analise adequada da eficacia do HI.

Uso terapeutico do hidroclorato de ioimbina em disfunçao eretil / Therapeutic use of yohimbine hydrochloride in erectile dysfunction

47 pacientes com disfunçao eretil foram selecionados para o uso de Hidroclorato de Ioimbina na dose de 20 mg/dia, por periodo minimo de 90 dias. Todos os pacientes foram submetidos a anamnese, exame fisico e exames propedeuticos especificos. A avaliaçao apos o uso da Ioimbina revelou que 17 por cento (9/47) dos pacientes apresentaram melhora subjetiva na qualidade da ereçao, sendo que 9 por cento (5/47) apresentaram resposta completa e 8 por cento (4/47) resposta parcial, e 83 por cento (38/47) nao obtiveram resposta. A avaliaçao comparativa dos resultados de disfunçoes organicas e psicogenicas mostraram que nos primeiros as respostas foram insignificantes, enquanto que dos 19 pacientes do grupo psicogenico, 5 (26 por cento) apresentaram respostas, a maioria completa. Conclui-se que a Ioimbina tem uma açao modesta na disfunçao eretil de origem organica e que so deve ser utilizada em pacientes de origem psicogenica ou aqueles com problemas organicos que nao aceitam outros metodos terapeuticos

Tratamento da disfuncao eretil masculina de origem organica - revisao / Organic male sexual disfunction treatment

Os autores fazem uma revisao sobre o tratamento cirurgico e nao cirurgico da disfuncao sexual masculinna organica. Enfatizam que melhores resultados podem ser obtidos se um diagnostico exato for feito. Medidas terapeuticas devem ser oferecidas ao paciente de acordo com a extensao de sua doenca e idade, comecando por procedimentos menos agressivos