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1.
Phytomedicine ; 21(11): 1382-9, 2014 Sep 25.
Artigo em Inglês | MEDLINE | ID: mdl-25022210

RESUMO

INTRODUCTION: It was the aim of the present experiments to examine potential antidiabetic effects of the Cimicifuga racemosa extract Ze 450. METHODS: Ze 450 and some of its components (23-epi-26-deoxyactein, protopine and cimiracemoside C) were investigated in vitro for their effects on AMP-activated protein kinase (AMPK) compared to metformin in HepaRG cells. Ze 450 (given orally (PO) and intraperitonally (IP)), metformin (PO) and controls were given over 7 days to 68 male ob/ob mice. Glucose and insulin concentrations were measured at baseline and during an oral glucose tolerance test (OGTT). RESULTS: Ze 450 and its components activated AMPK to the same extent as metformin. In mice, Ze 450 (PO/IP) decreased significantly average daily and cumulative weight gain, average daily food and water intake, while metformin had no effect. In contrast to metformin, PO Ze 450 virtually did not change maximum glucose levels during OGTT, however, prolonged elimination. Ze 450 administered PO and IP decreased significantly post-stimulated insulin, whereas metformin did not. HOMA-IR index of insulin resistance improved significantly after IP and PO Ze 450 and slightly after metformin. In summary, the results demonstrate that Ze 450 reduced significantly body weight, plasma glucose, improved glucose metabolism and insulin sensitivity in diabetic ob/ob mice. In vitro experiments suggest that part of the effects may be related to AMPK activation. CONCLUSIONS: Ze 450 may have utility in the treatment of type 2 diabetes. However, longer term studies in additional animal models or patients with disturbed glucose tolerance or diabetes may be of use to investigate this further.


Assuntos
Cimicifuga/química , Hipoglicemiantes/farmacologia , Extratos Vegetais/farmacologia , Proteínas Quinases Ativadas por AMP/metabolismo , Animais , Benzofenantridinas/farmacologia , Alcaloides de Berberina/farmacologia , Glicemia/metabolismo , Peso Corporal , Linhagem Celular , Diabetes Mellitus Tipo 2/tratamento farmacológico , Modelos Animais de Doenças , Teste de Tolerância a Glucose , Glicosídeos/farmacologia , Humanos , Insulina/sangue , Resistência à Insulina , Masculino , Metformina/farmacologia , Camundongos Obesos , Saponinas/farmacologia , Triterpenos/farmacologia
2.
Br J Ophthalmol ; 79(9): 830-3, 1995 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-7488602

RESUMO

BACKGROUND: A variety of autogenous and alloplastic materials have been used as subperiosteal implants to correct anophthalmic enophthalmos. Proplast II is a synthetic porous composite of Teflon polymer and alumina. Proplast II offers a number of advantages over other commonly used alloplastic materials such as silicone and polymethyl methacrylate. It is light, porous, resilient, malleable, and easy to shape. It can be readily sterilised after shaping. It has been found to integrate with the surrounding tissues, thereby minimising the risk of subsequent implant migration and extrusion. METHODS: Proplast II was used as a subperiosteal implant in a total of 15 anophthalmic patients during the period June 1990 to March 1994. The indication for this procedure in all patients was poor orbital volume replacement despite the prior insertion of an adequately sized spherical socket implant. RESULTS: The results were excellent with a good correction of preoperative upper eyelid sulcus deformity. There were no operative complications nor any serious postoperative complications. The implants were well tolerated. CONCLUSION: Proplast II can be highly recommended for use as a subperiosteal implant.


Assuntos
Óxido de Alumínio/uso terapêutico , Materiais Biocompatíveis/uso terapêutico , Enoftalmia/cirurgia , Proplast/análogos & derivados , Próteses e Implantes , Adulto , Idoso , Enoftalmia/complicações , Doenças Palpebrais/etiologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Proplast/uso terapêutico
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