This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Oral hypoglycaemic agents

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

These agents are only used when dietary treatment alone has failed *

Types of oral hypoglycaemic agents include:

  • sulphonylureas which work by increasing beta cell sensitivity to glucose thus increasing insulin release at a given plasma glucose concentration. This leads directly to a reduction in hepatic glucose production and indirectly, via a lowering of plasma glucose concentration, to decreased peripheral insulin resistance

  • biguanides e.g. metformin - which work by reducing hepatic glucose production. There are also a number of other effects reported including stimulation of peripheral glucose uptake, enhancement of insulin receptor binding and reduction of glucose absorption from the intestine. These are less important mechanisms of action

  • glitazones - this is a class of drugs which reverse the insulin resistance seen in type 2 diabetes. There is currently one licensed drug in this class, pioglitazone. The effect of the thiazolidinediones is mediated by the activation of a transcription regulator called peroxisome proliferator-activated receptor gamma (PPAR-gamma). This action modulates adipogenesis and carbohydrate metabolism in adipocytes and skeletal muscle. The only drug in this class in the UK is pioglitazone

  • alpha-glucosidase inhibitors e.g. acarbose - reversibly antagonise and slow the action of sucrase, glucoamylase, dextrinase, maltase and isomaltase enzymes within the intestinal tract. This hinders the production of absorbable monosaccharidases and so reduces the postprandial blood glucose concentration

  • meglitinides e.g repaglinide, nateglinide - lower blood glucose by stimulation of insulin release from the pancreas

  • gliptins e.g. sitagliptin, linagliptin - work via slowing degradation incretin hormones**

  • SGLT 2 inhibitors - a sodium-glucose cotransporter-2 (SGLT-2) inhibitor that blocks the reabsorption of glucose in the kidneys and promotes excretion of excess glucose in the urine (examples of this class include dapagliflozin, canagliflozin, empagliflozin)

  • oral semaglutide - an oral once daily GLP-1 analogue is available as a treatment option in type 2 diabetes

Note that in type 1 / insulin-dependent diabetes the essential therapy is insulin. Some oral hypoglycemic agents, such as metformin, may be used in addition in the management of patients with Type 1 diabetes.

Notes:

  • * Latent Autoimmune Diabetes of Adulthood (LADA) may initially present as presumed type 2 diabetes
    • is an example of a ketosis-prone diabetes and these patients may require early initiation of insulin therapy (rather than oral hypoglycaemic agents) as the pathological process relating to development of diabetes is insulin deficiency rather than insulin resistance
  • ** incretin hormones - for example glucagon-dependent insulinotropic peptide (GIP) and glucagon-like peptide-1 (GLP-1) - these hormones are secreted by specialised enteroendocrine cells in response to a meal. The incretin hormones promote insulin secretion and inhibit glucagon secretion when blood glucose is high; when blood glucose is low then insulin secretion is inhibited and glucagon secretion is promoted

Create an account to add page annotations

Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed when you visit this page

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.