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1.
Circulation ; 123(2): 186-94, 2011 Jan 18.
Artigo em Inglês | MEDLINE | ID: mdl-21200001

RESUMO

BACKGROUND: Adipose tissue expands in response to excess caloric intake, but individuals prone to deposit visceral instead of subcutaneous adipose tissue have higher risk of metabolic disease. The role of angiogenesis in the expandability of human adipose tissue depots is unknown. The objective of this study was to measure angiogenesis in visceral and subcutaneous adipose tissue and to establish whether there is a relationship between obesity, metabolic status, and the angiogenic properties of these depots. METHODS AND RESULTS: Angiogenic capacity was determined by quantifying capillary branch formation from human adipose tissue explants embedded in Matrigel, and capillary density was assessed by immunohistochemistry. Subcutaneous adipose tissue had a greater angiogenic capacity than visceral tissue, even after normalization to its higher initial capillary density. Gene array analyses revealed significant differences in expression of angiogenic genes between depots, including an increased subcutaneous expression of angiopoietin-like protein 4, which is proangiogenic in an adipose tissue context. Subcutaneous capillary density and angiogenic capacity decreased with morbid obesity, and subcutaneous, but not visceral, adipose tissue angiogenic capacity correlated negatively with insulin sensitivity. CONCLUSIONS: These data imply that subcutaneous adipose tissue has a higher capacity to expand its capillary network than visceral tissue, but this capacity decreases with morbid obesity. The decrease correlates with insulin resistance, suggesting that impairment of subcutaneous adipose tissue angiogenesis may contribute to metabolic disease pathogenesis.


Assuntos
Gordura Intra-Abdominal/irrigação sanguínea , Neovascularização Patológica/fisiopatologia , Neovascularização Fisiológica/fisiologia , Obesidade/fisiopatologia , Gordura Subcutânea/irrigação sanguínea , Adulto , Proteína 4 Semelhante a Angiopoietina , Angiopoietinas/metabolismo , Índice de Massa Corporal , Derivação Gástrica , Humanos , Resistência à Insulina/fisiologia , Gordura Intra-Abdominal/metabolismo , Gordura Intra-Abdominal/fisiopatologia , Pessoa de Meia-Idade , Obesidade/metabolismo , Obesidade/cirurgia , Gordura Subcutânea/metabolismo , Gordura Subcutânea/fisiopatologia
2.
Endocr Pract ; 16(1): 107-11, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-19625246

RESUMO

OBJECTIVE: To describe the successful treatment of severe noninsulinoma hyperinsulinemic hypoglycemia with use of a calcium channel blocking agent in an adult patient who had previously undergone a gastric bypass surgical procedure. METHODS: A 65-year-old woman who had undergone a gastric bypass surgical procedure 26 years earlier was hospitalized because of severe postprandial hypoglycemia. During and after hospitalization, the patient underwent assessment with conventional measurements of glucose, insulin, proinsulin, and C-peptide; toxicologic studies; magnetic resonance imaging studies of the pancreas; and determination of hepatic vein insulin concentrations after selective splanchnic artery calcium infusion. RESULTS: Metabolic variables were consistent with the diagnosis of hyperinsulinemic hypoglycemia. Magnetic resonance imaging revealed the presence of a side branch intraductal papillary mucinous tumor that had been stable for more than 1 year. The results of the calcium-stimulated insulin release study were consistent with nonlocalized hypersecretion of insulin. A trial of frequent small feedings failed to prevent hypoglycemia. On the basis of reports of successful treatment of childhood nesidioblastosis, the patient was then prescribed nifedipine, 30 mg daily. She has subsequently remained free of symptomatic hypoglycemia for 20 months. CONCLUSION: A calcium channel blocking agent may be efficacious and a potential alternative to partial pancreatectomy in cases of noninsulinoma hyperinsulinemic hypoglycemia in adults.


Assuntos
Hiperinsulinismo/diagnóstico , Hipoglicemia/diagnóstico , Nifedipino/uso terapêutico , Idoso , Feminino , Humanos , Hiperinsulinismo/tratamento farmacológico , Hipoglicemia/tratamento farmacológico
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