Ultrasound associated with caffeine increases basal and beta-adrenoceptor response in adipocytes isolated from subcutaneous adipose tissue in pigs.

BACKGROUND: The topical use of caffeine has been indicated for the lipodystrophies treatment as it promotes increased lipolysis. Ultrasound (US) is often used in cutaneous diseases, esthetic conditions, and as a skin permeation enhancer. OBJECTIVE: We investigate the lipolytic response of adipocytes isolated from subcutaneous adipose pigs tissue subjected to treatment with topical application of phonophoresis associated with caffeine. METHOD: We treated dorsal regions of pigs (Landrace × Large White, 35 days, 15 kg, n = 6) daily for 15 days with gel, gel + US [3 MHz, continuous, 0.2 Wcm(2), 1 min/cm(2), in total 2 min], gel + caffeine (5%w/w), and gel + caffeine + US. We used a fifth untreated region as control. Twenty-four hours after the last application, we isolated the adipocytes of each treated area and quantified the basal and stimulated lipolytic responses to isoprenaline. The results, in µmol glycerol/10(6)cells/60 min, were analyzed with analysis of variance or ANOVA followed by Newman-Keuls test. The value of p < 0.05 was indicative of statistical difference. RESULTS: Only the adipocytes isolated from the area treated with caffeine + US showed increased basal lipolysis (0.76 ± 0.26; p = 0.0276) and maximal isoprenaline stimulation (0.38 ± 0.15, p = 0.0029) compared with the other areas. CONCLUSION: The results demonstrate that increased lipolysis of caffeine + US is due to an increase in basal and beta-adrenoceptor response by caffeine, and caffeine's effect is local, avoiding unwanted effects.

Sensitivity to beta-adrenoceptor agonists of adipocytes from rats treated with an aqueous extract of Croton cajucara Benth.

Aqueous extracts of Croton cajucara bark are used in folk medicine to treat hepatic and gastrointestinal disorders and as a coadjuvant in weight-loss programs. We examined the effect of treating rats for 15 days with a 5% aqueous extract of C. cajucara on body weight and food intake. The epididymal adipose pads were removed and the lipolytic responses of isolated adipocytes to isoprenaline, noradrenaline (norepinephrine), BRL37344 and adrenaline (epinephrine) were analysed in the absence or presence of metoprolol or ICI118,551. Treated rats had a significantly lower weight gain than control rats, with no difference in food and liquid intake, epididymal fat-pad weight or basal glycerol release. The sensitivity of the lipolytic response to isoprenaline and adrenaline was significantly higher in adipocytes from treated rats. The sensitivity to noradrenaline or BRL37344 was unaltered. Metoprolol shifted the dose-response curves to noradrenaline to the right in adipocytes from control and treated rats; the dose-response curve to isoprenaline in adipocytes from control rats was also shifted to the right. In adipocytes from treated rats, the dose-response curve to isoprenaline was unaltered by metoprolol but was shifted to the right by ICI118,551, a beta(2)-adrenoceptor antagonist. We conclude that in adipocytes from treated rats there is an increase in the lipolytic response to non-selective agonists (isoprenaline and adrenaline) mediated by beta(2)-adrenoceptors, with no alteration in the responses mediated by beta(1)-adrenoceptors (noradrenaline) or beta(3)-adrenoceptors (BRL37344). This effect could increase the role of adrenaline as an endogenous stimulator of lipolysis.

Alterações Cardiometabólicas em Ratos Wistar Alimentados com Dieta Hiperlipídica e Hipercolesterolêmica por Seis Semanas / Cardiometabolic Alterations in Wistar Rats on a Six-Week Hyperlipidic, Hypercholesterolemic Diet

Fundamento: Alta ingestão de lipídeos e colesterol compõe a dieta da sociedade moderna e está envolvida com o desenvolvimento de doenças cardiometabólicas. Entretanto, há lacunas na literatura quanto à existência de modelos de dislipidemias em ratos Wistar. Objetivos: Analisar o perfil cardiometabólico de ratos Wistar alimentados com dieta hiperlipídica e hipercolesterolêmica por seis semanas. Métodos: Ratos Wistar jovens foram alimentados com dieta hiperlipídica e hipercolesterolêmica por seis semanas para induzir a hiperlipidemia. Os ratos foram submetidos à cateterização da artéria carótida para determinar a pressão arterial. Após jejum, amostras de sangue foram coletadas por meio do cateter, e as concentrações de colesterol total, colesterol HDL, triglicerídeos e glicose foram determinadas. Amostras do tecido cardíaco foram removidas para análise histológica, a fim de se verificar a hipertrofia ventricular. Resultados: A ingestão da dieta por seis semanas foi eficaz em induzir alterações cardiometabólicas. O perfil dislipidêmico apresentado pelos ratos Wistar foi acompanhado de hiperinsulinemia, hipertensão moderada e hipertrofia ventricular do coração. Não houve alterações na glicemia. Conclusões: A administração de dieta hiperlipídica e hipercolesterolêmica em ratos Wistar jovens por seis semanas induziram alterações cardiometabólicas tornando-se um modelo eficaz para distúrbios dessa natureza

Background: The diet of modern society is composed by large intakes of lipids and cholesterol, involved in the development of cardiometabolic diseases. However, there are gaps in the literature regarding the existence of dyslipidemia models in Wistar rats. Objectives: To analyze the cardiometabolic profile of Wistar rats on a six-week hyperlipidic, hypercholesterolemic diet. Methods: Young Wistar rats were kept on a hyperlipidic, hypercholesterolemic diet for six weeks to induce hyperlipidemia. The rats underwent catheterization of the carotid artery to determine blood pressure. After fasting, blood samples were drawn through the catheter, and concentrations of total cholesterol, HDL cholesterol, triglycerides and glucose were determined. Cardiac tissue samples were taken for a histological analysis to check for ventricular hypertrophy. Results: The six-week diet was effective in inducing cardiometabolic alterations. The dyslipidemic profile presented by the Wistar rats was accompanied by hyperinsulinemia, moderate hypertension and cardiac ventricular hypertrophy. There were no alterations in glycemia. Conclusion: The six-week hyperlipidic, hypercholesterolemic diet in young Wistar rats induced cardiometabolic alterations, becoming an effective model for disorders of this nature