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Related Concept Videos

Oral Hypoglycemic Agents: Sulfonylureas01:17

Oral Hypoglycemic Agents: Sulfonylureas

Sulfonylureas are oral hypoglycemic agents utilized in treating type 2 diabetes. They are characterized by their unique sulfonylurea chemical structure. The family of sulfonylureas is divided into generations. First-generation sulfonylureas, including tolbutamide (Orinase), chlorpropamide (Diabinese), and tolazamide (Tolinase), trigger insulin release from pancreatic β cells and enhance peripheral tissues' insulin sensitivity. The second-generation members, such as glipizide (Glucotrol),...
Oral Hypoglycemic Agents: Biguanides and Glitazones01:26

Oral Hypoglycemic Agents: Biguanides and Glitazones

Biguanides, particularly metformin (Glucophage), are insulin sensitizers that enhance glucose uptake, thereby reducing insulin resistance. Unlike sulfonylureas, metformin doesn't prompt insulin secretion, which helps to curb hypoglycemia risk. Metformin is beneficial in treating conditions like polycystic ovary syndrome due to its insulin-resistance reduction capability. The drug's primary action involves curtailing hepatic gluconeogenesis, a significant contributor to high blood glucose levels...
Oral Hypoglycemic Agents: Glinides01:06

Oral Hypoglycemic Agents: Glinides

Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively manages...
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors01:19

Oral Hypoglycemic Agents: α-Glucosidase Inhibitors

α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are typically...
Hypoglycemia and Glucagon01:15

Hypoglycemia and Glucagon

Without prolonged fasting, healthy individuals maintain blood glucose levels above 3.5 mM due to a well-adapted neuroendocrine counterregulatory system that effectively prevents acute hypoglycemia, a potentially life-threatening condition. The primary clinical scenarios for hypoglycemia encompass diabetes treatment, inappropriate production of endogenous insulin or insulin-like substances by tumors, and the use of glucose-lowering agents in non-diabetic individuals. Notably, hypoglycemia in the...
Hypoglycemia01:26

Hypoglycemia

Hypoglycemia is a blood glucose level below 70 mg/dL. It commonly occurs in individuals using insulin or insulin-secreting drugs, but may also arise in non-diabetic conditions. People with type 1 diabetes are at the highest risk because they depend on exogenous insulin. People with type 2 diabetes are also at risk, especially when treated with insulin or medications such as sulfonylureas, which increase insulin release regardless of blood glucose levels. It develops when insulin levels exceed...

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Related Experiment Video

Updated: Jul 19, 2026

Improving IV Insulin Administration in a Community Hospital
12:08

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Published on: June 11, 2012

Oral hypoglycaemic agents: the first thirty years.

J D Nabarro1

  • 1Middlesex Hospital, London.

Journal of the Royal College of Physicians of London
|January 1, 1992
PubMed
Summary

Oral hypoglycaemic agents (OHAs) were used in over 1,300 patients with non-insulin dependent diabetes (NIDDM). While many achieved control, some developed complications or required insulin, with a 5% annual secondary failure rate.

Area of Science:

  • Endocrinology
  • Metabolic Diseases
  • Pharmacology

Background:

  • Non-insulin dependent diabetes mellitus (NIDDM) management has evolved significantly.
  • Oral hypoglycaemic agents (OHAs) have been a cornerstone in NIDDM treatment for decades.
  • Understanding long-term outcomes of OHA use is crucial for patient care.

Purpose of the Study:

  • To describe the long-term outcomes of oral hypoglycaemic agent (OHA) treatment in a large cohort of patients with non-insulin dependent diabetes (NIDDM).
  • To evaluate the efficacy, secondary failure rates, and complications associated with OHA therapy.
  • To assess the use of OHAs in insulin dependent diabetes (IDDM) in early disease stages.

Main Methods:

  • Retrospective analysis of 1,333 NIDDM patients treated with OHAs between 1956 and 1988.

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  • Inclusion of 137 insulin dependent diabetes (IDDM) patients treated with OHAs.
  • Follow-up data collection over a 32-year period to assess control, complications, and treatment changes.
  • Main Results:

    • 51% of NIDDM patients on OHAs achieved satisfactory control; 262 died, 223 switched to insulin, and 41 stopped OHAs.
    • Annual secondary failure rate was approximately 5% between years 1 and 20.
    • NIDDM patients on OHAs showed higher rates of neuropathy, peripheral vascular disease, and coronary artery disease compared to insulin-treated patients.
    • 44% of IDDM patients treated with OHAs achieved good control for at least 12 months.

    Conclusions:

    • Long-term OHA use in NIDDM is associated with significant secondary failure rates and increased risk of microvascular and macrovascular complications.
    • While OHAs can be effective in early IDDM, long-term efficacy and safety require careful monitoring.
    • Side effects of OHAs were generally mild, with hypoglycemia, rashes, and gastrointestinal symptoms being infrequent.