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1.
Rev Endocr Metab Disord ; 22(4): 1013-1025, 2021 12.
Artículo en Inglés | MEDLINE | ID: mdl-33945051

RESUMEN

Obesity is a major public health problem worldwide. Only relatively few treatment options are, at present, available for the management of obese patients. Furthermore, treatment of obesity is affected by the widespread misuse of drugs and food supplements. Ephedra sinica is an old medicinal herb, commonly used in the treatment of respiratory tract diseases. Ephedra species contain several alkaloids, including pseudoephedrine, notably endowed with indirect sympathomimetic pharmacodynamic properties. The anorexigenic effect of pseudoephedrine is attributable primarily to the inhibition of neurons located in the hypothalamic paraventricular nucleus (PVN), mediating satiety stimuli. Pseudoephedrine influences lipolysis and thermogenesis through interaction with ß3 adrenergic receptors and reduces fat accumulation through down-regulation of transcription factors related to lipogenesis. However, its use is associated with adverse events that involve to a large extent the cardiovascular and the central nervous system. Adverse events of pseudoephedrine also affect the eye, the intestine, and the skin, and, of relevance, sudden cardiovascular death related to dietary supplements containing Ephedra alkaloids has also been reported. In light of the limited availability of clinical data on pseudoephedrine in obesity, along with its significantly unbalanced risk/benefit profile, as well as of the psychophysical susceptibility of obese patients, it appears reasonable to preclude the prescription of pseudoephedrine in obese patients of any order and degree.


Asunto(s)
Alcaloides , Ephedra sinica , Efedrina/efectos adversos , Humanos , Obesidad/inducido químicamente , Obesidad/tratamiento farmacológico , Seudoefedrina/uso terapéutico
2.
Arch Ital Urol Androl ; 89(1): 17-21, 2017 Mar 31.
Artículo en Inglés | MEDLINE | ID: mdl-28403589

RESUMEN

BACKGROUND: Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) is a complex condition, characterized by uncertain etiology and by limited response to therapy. The definition of CP/CPPS includes genitourinary pain with or without voiding symptoms in the absence of uropathogenic bacteria, as detected by standard microbiological methods, or another identifiable cause such as malignancy. The efficacy of various medical therapies, has been evaluated in clinical studies, but evidence is lacking or conflicting. We compared Serenoa Repens in monotherapy versus Palmitoylethanolamide (PEA) in combination with Alpha-lipoic acid (ALA) and evaluated the efficacy of these treatments in patients with CP/CPPS. METHODS: We conducted a randomized, single-blind trial. 44 patients diagnosed with CP/CPPS (mean age 41.32 ± 1.686 years) were randomly assigned to treatment with Palmitoylethanolamide 300 mg plus Alpha-lipoic acid 300 mg (Peanase®), or Serenoa Repens at 320 mg. Three questionnaires (NIH-CPSI, IPSS and IIEF5) were administered at baseline and after 12 weeks of treatment in each group. RESULTS: 12 week treatment with Peanase significantly improved the IPSS score compared to the same period of treatment with Serenoa Repens, and significantly reduced NIH-CPSI score. Similar results were observed in the different NIH-CPSI subscores break down. However, the same treatment did not result in significant improvement of the IIEF5 score. Both treatments did not produce undesired effects. CONCLUSIONS: The present results document the efficacy of an association of Palmitoylethanolamide (PEA) and Alpha-lipoic acid (ALA) administered for 12 weeks for treating patients with CP/CPPS, compared with Serenoa Repens monotherapy.


Asunto(s)
Etanolaminas/administración & dosificación , Ácidos Palmíticos/administración & dosificación , Dolor Pélvico/tratamiento farmacológico , Extractos Vegetales/administración & dosificación , Prostatitis/tratamiento farmacológico , Ácido Tióctico/administración & dosificación , Adulto , Amidas , Enfermedad Crónica , Dolor Crónico/tratamiento farmacológico , Humanos , Masculino , Persona de Mediana Edad , Serenoa/química , Método Simple Ciego , Encuestas y Cuestionarios , Resultado del Tratamiento , Adulto Joven
3.
Thyroid ; 20(12): 1351-8, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-20954817

RESUMEN

BACKGROUND: Sorafenib (BAY 43-9006) is an inhibitor of multiple-receptor tyrosine kinases involved in tumor growth and angiogenesis, which can be advantageously administered orally. Initially used as monotherapy in advanced renal cell carcinoma, sorafenib was proven to increase progression-free survival while enhancing disease control. Clinical trials on sorafenib are at present ongoing for the treatment of various malignancies, including thyroid cancer (TC). SUMMARY: Specifically, in two phase II studies recently conducted on papillary TC, although the respective results were not entirely compatible as regard partial response rate and progression-free survival, sorafenib demonstrated a relatively favorable benefit/risk profile. In another more recent phase II study, whose primary endpoint was the reinduction of radioactive iodine uptake at 26 weeks, although no reinduction of radioactive iodine uptake was observed, 59% had a beneficial response and 34% had stable disease. Sorafenib hence appears to be a valid alternative to conventional treatment of metastatic papillary TC refractory to radioiodine therapy. CONCLUSIONS: Further prospective investigations are required to define the characteristics of tumor response to the drug and the factors inducing resistance to treatment. A major issue demanding immediate attention involves optimization of sorafenib treatment: this concerns multidrug combination with different tyrosine kinase inhibitors or immunomodulating agents with the aim of reducing doses and thereby improving drug tolerability and antineoplastic capability.


Asunto(s)
Bencenosulfonatos/uso terapéutico , Carcinoma Papilar/tratamiento farmacológico , Piridinas/uso terapéutico , Antineoplásicos/uso terapéutico , Supervivencia sin Enfermedad , Interacciones Farmacológicas , Humanos , Niacinamida/análogos & derivados , Compuestos de Fenilurea , Proteínas Tirosina Quinasas/antagonistas & inhibidores , Sorafenib , Neoplasias de la Tiroides/tratamiento farmacológico , Neoplasias de la Tiroides/patología
4.
Nutr J ; 7: 29, 2008 Sep 30.
Artículo en Inglés | MEDLINE | ID: mdl-18826565

RESUMEN

This review will discuss some issues related to the risk/benefit profile of the use of dietary antioxidants. Thus, recent progress regarding the potential benefit of dietary antioxidants in the treatment of chronic diseases with a special focus on immune system and neurodegenerative disorders will be discussed here. It is well established that reactive oxygen species (ROS) play an important role in the etiology of numerous diseases, such as atherosclerosis, diabetes and cancer. Among the physiological defense system of the cell, the relevance of antioxidant molecules, such as glutathione and vitamins is quite well established. Recently, the interest of researchers has, for example, been conveyed on antioxidant enzyme systems, such as the heme oxygenase/biliverdin reductase system, which appears modulated by dietary antioxidant molecules, including polyphenols and beta-carotene. These systems possibly counteract oxidative damage very efficiently and finally modulate the activity of oxidative phenomena occurring, for instance, during pathophysiological processes. Although evidence shows that antioxidant treatment results in cytoprotection, the potential clinical benefit deriving from both nutritional and supplemental antioxidants is still under wide debate. In this line, the inappropriate assumption of some lipophylic vitamins has been associated with increased incidence of cancer rather than with beneficial effects.


Asunto(s)
Antioxidantes/efectos adversos , Sistema Inmunológico/efectos de los fármacos , Enfermedades Neurodegenerativas/prevención & control , Medición de Riesgo , Antioxidantes/farmacología , Suplementos Dietéticos , Humanos , Sistema Inmunológico/fisiología , Neoplasias/patología , Neoplasias/prevención & control , Enfermedades Neurodegenerativas/patología , Estrés Oxidativo/efectos de los fármacos , Especies Reactivas de Oxígeno/metabolismo , Resultado del Tratamiento
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