Diabetes & Blood Glucose Regulation
Blood glucose is precisely regulated between 70–100 mg/dL in the fasting state. This is achieved through the coordinated actions of hormones, primarily insulin and glucagon, acting on liver, muscle, and adipose tissue.
Hormonal Control
- Insulin (β-cells of islets of Langerhans): Anabolic hormone. Secreted in response to ↑blood glucose, GLP-1. Actions: ↑Glucose uptake (GLUT4 in muscle/fat), ↑Glycogenesis, ↑Glycolysis, ↑FA synthesis, ↑Protein synthesis; ↓Glycogenolysis, ↓Gluconeogenesis, ↓Lipolysis, ↓Ketogenesis.
- Glucagon (α-cells): Catabolic hormone. Secreted in response to ↓blood glucose, amino acids. Actions: ↑Glycogenolysis (liver), ↑Gluconeogenesis, ↑Lipolysis, ↑Ketogenesis; ↓Glycolysis, ↓FA synthesis.
- Cortisol: Raises blood glucose (induces gluconeogenic enzymes, stimulates lipolysis and proteolysis for substrates). Causes insulin resistance.
- Epinephrine: Stress hormone; rapid glycogenolysis (liver and muscle), lipolysis.
- Growth Hormone: Stimulates lipolysis; anti-insulin (diabetogenic in excess).
Diabetes Mellitus — Classification
- Type 1 DM (Insulin-dependent): Autoimmune destruction of β-cells → absolute insulin deficiency. Prone to diabetic ketoacidosis. Treatment: Insulin replacement.
- Type 2 DM (Non-insulin-dependent): Insulin resistance + relative insulin deficiency. Associated with obesity, aging. No ketoacidosis (some insulin present). Treatment: Lifestyle + Metformin/sulfonylureas/GLP-1 agonists; insulin if needed.
- Gestational DM: Diagnosed in pregnancy; risk of macrosomia, neonatal hypoglycemia.
- MODY: Maturity Onset Diabetes of the Young — monogenic, autosomal dominant.
Metabolic Changes in Diabetes
- ↑Blood glucose → glycosuria (exceeded renal threshold ~180 mg/dL) → osmotic diuresis → polyuria, polydipsia
- Lack of insulin → ↑Lipolysis → ↑FFA → ↑Ketogenesis (3 ketone bodies: Acetoacetate, β-Hydroxybutyrate, Acetone)
- Ketoacidosis: Blood pH drops → Kussmaul breathing (rapid deep breathing to blow off CO₂)
- Hyperglycemia → non-enzymatic glycosylation → HbA1c (3-month average glucose); AGEs cause vascular damage
Complications of Diabetes
- Microvascular: Retinopathy, Nephropathy (Kimmelstiel-Wilson lesion), Neuropathy
- Macrovascular: Accelerated atherosclerosis, MI, stroke, peripheral vascular disease
- Sorbitol pathway: Excess glucose → sorbitol (aldose reductase) → cataracts, neuropathy in DM
HbA1c
Non-enzymatic glycosylation of Hb. Reflects average blood glucose over previous 2–3 months (RBC lifespan ~120 days). Normal <5.7%; Prediabetes 5.7–6.4%; Diabetes ≥6.5%.