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1.
Physiol Behav ; 168: 11-19, 2017 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-27720901

RESUMO

Hyperlipidemia is a risk factor for the development of cognitive dysfunction and atherosclerosis. Natural compounds have recently received special attention in relation to the treatment of disease due to their low cost and wide margin of safety. Thus, the aim of this study was to determine the possible preventive effect of guarana powder (Paullinia cupana) on memory impairment and acetylcholinesterase (AChE) activity in the brain structures of rats with Poloxamer-407-induced hyperlipidemia. Adult male Wistar rats were pretreated with guarana (12.5, 25 and 50mg/kg/day) and caffeine (0.2mg/kg/day) by gavage for a period of 30days. Simvastatin (0.04mg/kg) was administered as a comparative standard. Acute hyperlipidemia was induced with intraperitoneal injections of 500mg/kg of Poloxamer-407. Memory tests and evaluations of anxiety were performed. The cortex, cerebellum, hippocampus, hypothalamus and striatum were separated to assess acetylcholinesterase activity. Our results revealed that guarana powder was able to reduce the levels of TC and LDL-C in a manner similar to simvastatin. Guarana powder also partially reduced the liver damage caused by hyperlipidemia. Guarana was able to prevent changes in the activity of AChE and improve memory impairment due to hyperlipidemia. Guarana powder may therefore be a source of promising phytochemicals that can be used as adjuvant therapy in the management of hyperlipidemia and cognitive disorders.


Assuntos
Acetilcolinesterase/metabolismo , Encéfalo/enzimologia , Cafeína/uso terapêutico , Hiperlipidemias , Poloxâmero/toxicidade , Tensoativos/toxicidade , Teobromina/uso terapêutico , Teofilina/uso terapêutico , Animais , Glicemia , Colesterol/sangue , Hiperlipidemias/induzido quimicamente , Hiperlipidemias/tratamento farmacológico , Hiperlipidemias/patologia , Masculino , Aprendizagem em Labirinto/efeitos dos fármacos , Paullinia/química , Extratos Vegetais/uso terapêutico , Ratos , Ratos Wistar , Reconhecimento Psicológico/efeitos dos fármacos , Estatísticas não Paramétricas
3.
J Hum Nutr Diet ; 14(3): 243-50, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11424516

RESUMO

BACKGROUND: Obesity and overweight may soon affect more than half of the population in some regions of the world and are associated with diabetes, hypertension and other diseases that cause morbidity, mortality and high health-care expenditure. No one approach, whether dietetic management, medication, or commercial weight loss programme, can alone solve the problem--all potential treatments need to be investigated and exploited. Among the herbal preparations known to non-western cultures are materials which may have applications in modulating physiological processes which influence gut motility, food intake and energy balance. One such mixed herbal preparation is 'YGD' containing Yerbe Maté (leaves of Ilex paraguayenis), Guarana (seeds of Paullinia cupana) and Damiana (leaves of Turnera diffusa var. aphrodisiaca). AIMS: This study had two distinct aims: to determine the effect of a herbal preparation 'YGD' containing Yerbe Maté, Guarana and Damiana on gastric emptying; to determine the effect of the same preparation on weight loss over 10 days and 45 days and weight maintenance over 12 months. METHODS: Gastric emptying was observed using ultrasound scanning in seven healthy volunteers following YGD and placebo capsules taken with 420 mL apple juice. Body weight was observed before and after 10 days of treatment with three YGD capsules or three placebo capsules before each meal for 10 days in 44 healthy overweight patients attending a primary health care centre. Forty-seven healthy overweight patients entered a double-blind placebo-controlled parallel trial of three capsules of YGD capsules before each main meal for 45 days compared with three placebo capsules on body weight. Body weight was monitored in 22 patients who continued active (YGD capsules) treatment for 12 months. RESULTS: The herb preparation YGD was followed by a prolonged gastric emptying time of 58 +/- 15 min compared to 38 +/- 7.6 min after placebo (P = 0.025). Body weight reductions were 0.8 +/- 0.05 kg after YGD capsules compared to 0.3 +/- 0.03 kg after placebo capsules over 10 days, and 5.1 +/- 0.5 kg after PGD capsules compared to 0.3 +/- 0.08 kg after placebo over 45 days. Active treatment with YGD capsules resulted in weight maintenance of the group (73 kg at the beginning and 72.5 kg at the end of 12 months). CONCLUSIONS: The herbal preparation, YGD capsules, significantly delayed gastric emptying, reduced the time to perceived gastric fullness and induced significant weight loss over 45 days in overweight patients treated in a primary health care context. Maintenance treatment given in an uncontrolled context resulted in no further weight loss, nor weight regain in the group as a whole. The herbal preparation is thus shown to be one that significantly modulates gastric emptying. Further clinical studies with dietetic monitoring of energy intake, dietary quality, satiety ratings, body weight and body composition are now indicated, and examination of the active principles contained in the three herbal components may prove rewarding.


Assuntos
Esvaziamento Gástrico/efeitos dos fármacos , Obesidade/tratamento farmacológico , Fitoterapia , Extratos Vegetais/uso terapêutico , Redução de Peso/efeitos dos fármacos , Cafeína/farmacologia , Cafeína/uso terapêutico , Método Duplo-Cego , Feminino , Humanos , Ilex paraguariensis/química , Masculino , Extratos Vegetais/farmacologia , Folhas de Planta/química , Sementes/química , Estômago/diagnóstico por imagem , Teobromina/farmacologia , Teobromina/uso terapêutico , Teofilina/farmacologia , Teofilina/uso terapêutico , Fatores de Tempo , Turnera/química , Ultrassonografia
4.
Brain Res ; 831(1-2): 315-8, 1999 Jun 12.
Artigo em Inglês | MEDLINE | ID: mdl-10412014

RESUMO

The influence of 3,7-dimethyl-1-propargylxanthine (DMPX) an adenosine A(2) receptor antagonist, was studied in the quinolinic acid (QA) model of Huntington's disease. Male Wistar rats received bilateral intrastriatal injections of QA (300 nmol) alone or plus DMPX (0.02, 0.2 and 2 microg). At the dose of 0.2 microg, DMPX completely prevented QA-induced EEG abnormalities at the level of frontal cortex. The results support the hypothesis of a neuroprotective role of adenosine A(2) receptor antagonists.


Assuntos
Corpo Estriado/metabolismo , Eletroencefalografia/efeitos dos fármacos , Lobo Frontal/efeitos dos fármacos , Doença de Huntington/tratamento farmacológico , Fármacos Neuroprotetores/uso terapêutico , Antagonistas de Receptores Purinérgicos P1 , Teobromina/análogos & derivados , Animais , Modelos Animais de Doenças , Masculino , Microinjeções , Ácido Quinolínico/toxicidade , Ratos , Ratos Wistar , Teobromina/uso terapêutico
5.
Clin Nucl Med ; 24(1): 29-34, 1999 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-9890490

RESUMO

PURPOSE: In normal aging persons, oxygen and glucose consumption progressively decreases with reduced cerebral blood flow (CBF), which could be responsible for age-related changes in cognitive functions. A data processing model with the use of Tc-99m SPECT of the human brain has been developed and found to be sensitive for monitoring the effects of drugs that increase CBF. In this study, the effect of two vasodilator drugs (the combination of pentifylline and nicotinic acid versus piracetam) was compared with the effect of placebo on CBF. MATERIALS AND METHODS: Thirty elderly volunteers had three different procedures using the Peelproc method to spatially standardize and compare CBF patterns by SPECT before and after drug intervention. The 30 patients were divided into five groups of six persons each who were randomly assigned in a 1:1 ratio to the treatment sequences consisting of three phases: the combination of pentifylline and nicotinic acid (C), piracetam (N), and placebo (P), or C-N-P; P-N-C; P-C-N; N-C-P; C-P-N; or N-P-C. Phases 1 to 3 each consisted of a baseline recording of parameters (day 0), treatment for 60 days (days 1 to 60), and recording of parameters after treatment (day 61). RESULTS: In elderly human volunteers (ages, 52 to 70 years), after 2 months of oral treatment with a combination of pentifylline and nicotinic acid (800 mg pentifylline, 200 mg nicotinic acid daily), SPECT results for the Peel-proc program indicated a statistically significant improvement in CBF of the total brain, with a more pronounced improvement in the cerebellum and frontal regions, where a definite shift from abnormal to normal blood flow was detected. Spontaneous communication from most of the volunteers suggested that they experienced an improvement in memory and general well-being from the combination treatment. After 2 months of oral treatment with piracetam (2.4 g daily) in elderly human volunteers, SPECT results indicated a regional improvement in CBF, particularly in the cerebellum. However, no beneficial effects with this drug were spontaneously reported. CONCLUSION: The in vivo method to quantitatively monitor the progress of long-term drug therapy on CBF described here could be useful to assess and even direct changes in therapy.


Assuntos
Encéfalo/diagnóstico por imagem , Circulação Cerebrovascular/efeitos dos fármacos , Nootrópicos/uso terapêutico , Tomografia Computadorizada de Emissão de Fóton Único , Administração Oral , Idoso , Envelhecimento/fisiologia , Encéfalo/efeitos dos fármacos , Encéfalo/metabolismo , Cerebelo/irrigação sanguínea , Cerebelo/diagnóstico por imagem , Cognição/efeitos dos fármacos , Cognição/fisiologia , Estudos Cross-Over , Demência/tratamento farmacológico , Combinação de Medicamentos , Lobo Frontal/irrigação sanguínea , Lobo Frontal/diagnóstico por imagem , Glucose/metabolismo , Humanos , Transtornos da Memória/tratamento farmacológico , Pessoa de Meia-Idade , Niacina/administração & dosagem , Niacina/uso terapêutico , Consumo de Oxigênio , Satisfação do Paciente , Piracetam/administração & dosagem , Piracetam/uso terapêutico , Placebos , Método Simples-Cego , Teobromina/administração & dosagem , Teobromina/análogos & derivados , Teobromina/uso terapêutico , Vasodilatadores/uso terapêutico
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