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Glucose intolerance in the carcinoid syndrome
Diabetes
|July 1, 1975
Summary
Patients with carcinoid syndrome exhibit impaired glucose tolerance and insulin secretion, linked to elevated serotonin levels. Serotonin antagonists and synthesis blockers partially improved these metabolic abnormalities.
Area of Science:
- Endocrinology
- Oncology
- Metabolic Research
Background:
- Carcinoid syndrome, often associated with metastatic carcinoid tumors, presents with elevated serotonin levels.
- Glucose intolerance and impaired insulin secretion are potential complications in patients with carcinoid syndrome.
Purpose of the Study:
- To investigate glucose tolerance and insulin secretion in patients with active carcinoid syndrome versus those with inactive tumors.
- To determine the role of serotonin in the metabolic alterations observed in carcinoid syndrome.
Main Methods:
- Assayed glucose tolerance and insulin secretion using intravenous glucose disposal rate constants (KG) and insulinogenic index.
- Administered serotonin antagonist cyproheptadine and serotonin synthesis inhibitor p-chlorophenylalanine to assess their effects.
- Evaluated the impact of streptozotocin treatment on glucose metabolism and insulin secretion.
Main Results:
- Patients with active carcinoid syndrome showed significantly lower KG values and impaired insulin secretion compared to normals.
- Serotonin antagonism and synthesis inhibition partially improved glucose disposal and insulin secretion.
- Insulin half-life was normal, suggesting impaired secretion, not accelerated destruction, as the cause of low insulin levels.
Conclusions:
- A high incidence (80%) of glucose intolerance and impaired insulin secretion occurs in carcinoid syndrome.
- Serotonin plays a significant role in causing these glucose metabolism and insulin secretion abnormalities.
- Streptozotocin treatment did not impair glucose tolerance or insulin secretion in the studied patients.