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1.
International Neurourology Journal ; : 83-89, 2018.
Artículo en Inglés | WPRIM | ID: wpr-715333

RESUMEN

PURPOSE: The urinary bladder (UB) is innervated by both sensory and autonomic nerves. Recent studies have shown that sensory neuropeptides induced contractions in the detrusor muscle. Therefore, in a mouse model, we investigated the presence of interactions between the submucosal sensory nerves and the autonomic nerves that regulate the motor function of the detrusor muscle. METHODS: UB samples from male C57BL/6 mice were isolated, cut into strips, and mounted in an organ bath. Dose-response curves to norepinephrine and phenylephrine were studied in UB strips with and without mucosa, and the effects of preincubation with a receptor antagonist and various drugs on relaxation were also studied using tissue bath myography. RESULTS: Phenylephrine-induced relaxation of the UB strips showed concentration-related effects. This relaxation appeared in both mucosa-intact and mucosa-denuded UB strips, and was significantly inhibited by lidocaine, silodosin, and guanethidine (an adrenergic neuronal blocker). Meanwhile, phenylephrine-induced relaxation was inhibited by pretreatment with propranolol and calcitonin gene-related peptide (CGRP)–depletory capsaicin in UB strips with and without mucosa. CONCLUSIONS: The present study suggests that phenylephrine activates the α-1A adrenergic receptor (AR) of the sensory nerve, and then activates capsaicin-sensitive sensory nerves to release an unknown substance that facilitates the release of norepinephrine from adrenergic nerves. Subsequently, norepinephrine stimulates β-ARs in the detrusor muscle in mice, leading to neurogenic relaxation of the UB. Further animal and human studies are required to prove this concept and to validate its clinical usefulness.


Asunto(s)
Animales , Humanos , Masculino , Ratones , Neuronas Adrenérgicas , Vías Autónomas , Baños , Péptido Relacionado con Gen de Calcitonina , Capsaicina , Guanetidina , Lidocaína , Membrana Mucosa , Miografía , Neuropéptidos , Norepinefrina , Fenilefrina , Propranolol , Receptores Adrenérgicos , Receptores Adrenérgicos alfa 1 , Relajación , Vejiga Urinaria
2.
International Neurourology Journal ; : 20-28, 2017.
Artículo en Inglés | WPRIM | ID: wpr-19908

RESUMEN

PURPOSE: The aim of this study was to assess the potential involvement of a specific subtype of 5-hydroxytryptamine (5-HT), 5HT(2) receptors in neurally-induced contractions of the human detrusor. METHODS: Contractile responses to electrical field stimulation (EFS) were examined in human isolated urinary bladder muscle strips. The potentiation of EFS-induced detrusor contraction was examined by adding cumulative concentrations of a 5-HT and 5-HT(2) receptor agonist, α-methyl-serotonin (α-Me-5-HT) (1nM–100μM) in the presence or absence of a 5-HT₂ antagonist, ketanserin (5-HT(2A)>5-HT(2C)) or naftopidil (5-HT(2B)>5-HT(2A)) (0.3–3μM). RESULTS: 5-HT and α-Me-5-HT potentiated EFS-induced contraction with a maximal effect (E(max)) of 37.6% and 38.6%, respectively, and with pEC(50) (negative logarithm of the concentration required for a half-maximal response to an agonist) values of 8.3 and 6.8, respectively. Neither ketanserin nor naftopidil at any concentration produced a rightward displacement of the α-Me-5-HT concentration response curve. Instead, the E(max) of α-Me-5-HT increased in the presence of ketanserin at 0.3–1μM and in the presence of naftopidil at 1μM to 51% and 56%, respectively, while the E(max) in the presence of vehicle alone was 36%. The highest concentration (3μM) of either drug, however, fully reversed the enhancement. CONCLUSIONS: The potentiating effect of α-Me-5-HT on neurally-induced contraction of human urinary bladder muscle strips was not found to be mediated via any 5-HT(2) receptor subtypes. The underlying mechanism for the enhancement of the α-Me-5-HT potentiating effect on detrusor contractility by ketanserin and naftopidil remains unknown; however, our results suggest that these drugs may be useful for treating contractile dysfunction of the detrusor, as manifested in conditions such as underactive bladder.


Asunto(s)
Humanos , Ketanserina , Prostatismo , Receptores Adrenérgicos alfa 1 , Receptores de Serotonina , Serotonina , Obstrucción del Cuello de la Vejiga Urinaria , Vejiga Urinaria
3.
Braz. j. med. biol. res ; 47(5): 411-418, 02/05/2014. tab, graf
Artículo en Inglés | LILACS | ID: lil-709437

RESUMEN

Transcutaneous electrical nerve stimulation (TENS) is a type of therapy used primarily for analgesia, but also presents changes in the cardiovascular system responses; its effects are dependent upon application parameters. Alterations to the cardiovascular system suggest that TENS may modify venous vascular response. The objective of this study was to evaluate the effects of TENS at different frequencies (10 and 100 Hz) on venous vascular reactivity in healthy subjects. Twenty-nine healthy male volunteers were randomized into three groups: placebo (n=10), low-frequency TENS (10 Hz, n=9) and high-frequency TENS (100 Hz, n=10). TENS was applied for 30 min in the nervous plexus trajectory from the superior member (from cervical to dorsal region of the fist) at low (10 Hz/200 μs) and high frequency (100 Hz/200 μs) with its intensity adjusted below the motor threshold and intensified every 5 min, intending to avoid accommodation. Venous vascular reactivity in response to phenylephrine, acetylcholine (endothelium-dependent) and sodium nitroprusside (endothelium-independent) was assessed by the dorsal hand vein technique. The phenylephrine effective dose to achieve 70% vasoconstriction was reduced 53% (P<0.01) using low-frequency TENS (10 Hz), while in high-frequency stimulation (100 Hz), a 47% increased dose was needed (P<0.01). The endothelium-dependent (acetylcholine) and independent (sodium nitroprusside) responses were not modified by TENS, which modifies venous responsiveness, and increases the low-frequency sensitivity of α1-adrenergic receptors and shows high-frequency opposite effects. These changes represent an important vascular effect caused by TENS with implications for hemodynamics, inflammation and analgesia.


Asunto(s)
Adulto , Humanos , Masculino , Acetilcolina/farmacología , Fármacos Cardiovasculares/farmacología , Mano/irrigación sanguínea , Nitroprusiato/farmacología , Fenilefrina/farmacología , Estimulación Eléctrica Transcutánea del Nervio/métodos , Análisis de Varianza , Glucemia , Colesterol/sangre , Recuento de Eritrocitos , Recuento de Leucocitos , Lipoproteínas HDL/sangre , Triglicéridos/sangre , Urea/sangre , Vasoconstricción/efectos de los fármacos , Vasoconstrictores/farmacología , Vasodilatación/efectos de los fármacos , Vasodilatadores/farmacología , Venas/efectos de los fármacos
4.
Anest. analg. reanim ; 22(1): 18-23, 2009. ilus
Artículo en Español | LILACS | ID: lil-694191

RESUMEN

resumen Se describen tres casos clínicos de Síndrome Doloroso Regional Complejo Tipo 1, cuya denominación anterior era distrofia simpático refleja.Se analizaron los síntomas y signos para lograr un diagnóstico positivo y los exámenes complementarios solicitados en vistas a sostener el diagnóstico. Se mostraron los resultados del tratamiento destacándose la alta efectividad de nitroglicerina en parches transdérmicos.


summary We described three clinical cases with Complex Regional Pain Syndrome type 1, previously named Reflex Sympathetic Dystrophy, the symptoms and signs were analyzed looking for the diagnosis as well as the complementary studies needed to support it. Finally we showed the efficacy of the treatment with transdermic patches of nitro-glycerine, reaching very good and excellent results.


resumo Descreven-se 3 casos clínicos de Síndrome e Dolorosa Complexa Tipo 1, cuja denominação anterior era Distrofia Simpático Reflexa. Se analisaram os sintomas e sinais para chegar à um diagnóstico positivo e os exames complementares solicitados com vistas a sustentar o diagnóstico. Mostrar-se os resultados do tratamento destacando-se a alta efetividade da Nitroglicerina em adesivos transdérmicos.

5.
Chinese Journal of Urology ; (12)2006.
Artículo en Chino | WPRIM | ID: wpr-544402

RESUMEN

500 mg,frequency was reduced in rats treated with tamsulosin (P500 mg,and the combined ?1a/?1dAR antagonist tamsulosin reduces urinary frequency more than the ?1aAR selective antagonist 5MU.This finding supports the hypothesis that the ?1dAR is important in mediating irritative symptoms.

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