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Differential selectivity of insulin secretagogues: Mechanisms, clinical implications, and drug interactions
by
Gribble, Fiona M
, Reimann, Frank
in
Adenosine triphosphatase
/ Adenosine Triphosphate - physiology
/ Animals
/ ATP sensitive potassium channel (K ATP channel)
/ ATP-Binding Cassette Transporters
/ Diabetes Mellitus, Type 2 - drug therapy
/ Drug Interactions
/ Humans
/ Insulin - metabolism
/ Insulin Secretion
/ Ion Channel Gating
/ Islets of Langerhans - drug effects
/ Islets of Langerhans - metabolism
/ Muscular system
/ Organ Specificity
/ Potassium
/ Potassium Channels - drug effects
/ Potassium Channels - physiology
/ Potassium Channels, Inwardly Rectifying
/ Protein Conformation
/ Protein Subunits
/ Proteins
/ Receptors, Drug - drug effects
/ Receptors, Drug - physiology
/ Rodents
/ Sulfonylurea Compounds - pharmacology
/ Sulfonylurea Compounds - therapeutic use
/ Sulfonylurea Receptors
/ Sulphonylurea
/ Sulphonylurea receptor
/ Xenopus
2003
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Differential selectivity of insulin secretagogues: Mechanisms, clinical implications, and drug interactions
by
Gribble, Fiona M
, Reimann, Frank
in
Adenosine triphosphatase
/ Adenosine Triphosphate - physiology
/ Animals
/ ATP sensitive potassium channel (K ATP channel)
/ ATP-Binding Cassette Transporters
/ Diabetes Mellitus, Type 2 - drug therapy
/ Drug Interactions
/ Humans
/ Insulin - metabolism
/ Insulin Secretion
/ Ion Channel Gating
/ Islets of Langerhans - drug effects
/ Islets of Langerhans - metabolism
/ Muscular system
/ Organ Specificity
/ Potassium
/ Potassium Channels - drug effects
/ Potassium Channels - physiology
/ Potassium Channels, Inwardly Rectifying
/ Protein Conformation
/ Protein Subunits
/ Proteins
/ Receptors, Drug - drug effects
/ Receptors, Drug - physiology
/ Rodents
/ Sulfonylurea Compounds - pharmacology
/ Sulfonylurea Compounds - therapeutic use
/ Sulfonylurea Receptors
/ Sulphonylurea
/ Sulphonylurea receptor
/ Xenopus
2003
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Differential selectivity of insulin secretagogues: Mechanisms, clinical implications, and drug interactions
by
Gribble, Fiona M
, Reimann, Frank
in
Adenosine triphosphatase
/ Adenosine Triphosphate - physiology
/ Animals
/ ATP sensitive potassium channel (K ATP channel)
/ ATP-Binding Cassette Transporters
/ Diabetes Mellitus, Type 2 - drug therapy
/ Drug Interactions
/ Humans
/ Insulin - metabolism
/ Insulin Secretion
/ Ion Channel Gating
/ Islets of Langerhans - drug effects
/ Islets of Langerhans - metabolism
/ Muscular system
/ Organ Specificity
/ Potassium
/ Potassium Channels - drug effects
/ Potassium Channels - physiology
/ Potassium Channels, Inwardly Rectifying
/ Protein Conformation
/ Protein Subunits
/ Proteins
/ Receptors, Drug - drug effects
/ Receptors, Drug - physiology
/ Rodents
/ Sulfonylurea Compounds - pharmacology
/ Sulfonylurea Compounds - therapeutic use
/ Sulfonylurea Receptors
/ Sulphonylurea
/ Sulphonylurea receptor
/ Xenopus
2003
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Differential selectivity of insulin secretagogues: Mechanisms, clinical implications, and drug interactions
Journal Article
Differential selectivity of insulin secretagogues: Mechanisms, clinical implications, and drug interactions
2003
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Overview
The sulphonylurea receptor (SUR) subunits of K
ATP channels are the targets for several classes of therapeutic drugs. Sulphonylureas close K
ATP channels in pancreatic β-cells and are used to stimulate insulin release in type 2 diabetes, whereas the K
ATP channel opener nicorandil acts as an antianginal agent by opening K
ATP channels in cardiac and vascular smooth muscle. The predominant type of SUR varies between tissues: SUR1 in β-cells, SUR2A in cardiac muscle, and SUR2B in smooth muscle. Sulphonylureas and related drugs exhibit differences in tissue specificity, as the drugs interact to varying degrees with different types of SUR. Gliclazide and tolbutamide are β-cell selective and reversible. Glimepiride, glibenclamide, and repaglinide, however, inhibit cardiac and smooth muscle K
ATP channels in addition to those in β-cells and are only slowly reversible. Similar properties have been observed by recording K
ATP channel activity in intact cells and in
Xenopus oocytes expressing cloned K
ATP channel subunits. While K
ATP channels in cardiac and smooth muscle are largely closed under physiological conditions (but open during ischaemia), they are activated by antianginal agents such as nicorandil. Under these conditions, they may be inhibited by sulphonylureas that block SUR2-type K
ATP channels (e.g., glibenclamide). Care should, therefore, be taken when choosing a sulphonylurea if potential interactions with cardiac and smooth muscle K
ATP channels are to be avoided.
Publisher
Elsevier Inc,Elsevier Limited
Subject
/ Adenosine Triphosphate - physiology
/ Animals
/ ATP sensitive potassium channel (K ATP channel)
/ ATP-Binding Cassette Transporters
/ Diabetes Mellitus, Type 2 - drug therapy
/ Humans
/ Islets of Langerhans - drug effects
/ Islets of Langerhans - metabolism
/ Potassium Channels - drug effects
/ Potassium Channels - physiology
/ Potassium Channels, Inwardly Rectifying
/ Proteins
/ Receptors, Drug - drug effects
/ Receptors, Drug - physiology
/ Rodents
/ Sulfonylurea Compounds - pharmacology
/ Sulfonylurea Compounds - therapeutic use
/ Xenopus
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