Pharmacokinetics of leptin in female mice

Title:

Pharmacokinetics of leptin in female mice

Creator:

Hart, R. A., Dobos, R. C., Agnew, L. L., Tellam, R. L., and McFarlane, J. R.

Identifier:

https://cdk.lib.cas.cz/client/handle/uuid:3b04e54a-ec25-4fc4-9904-a109da8b3e94
uuid:3b04e54a-ec25-4fc4-9904-a109da8b3e94
issn:0862-8408

Subject:

Fyziologie člověka a srovnávací fyziologie, leptin, farmakokinetika, eliminace (chemie), pharmacokinetics, elimination, distribution, periphery, 14, and 612

Type:

article, články, model:article, and TEXT

Format:

print, bez média, and svazek

Description:

Pharmacokinetics of leptin in mammals has received limited attention and only one study has examined more than two time points and this was in ob/ob mice. This study is the first to observe the distribution of leptin over a time course in female mice. A physiologic dose (12 ng) of radiolabelled leptin was injected in adult female mice via the lateral tail vein and tissues were dissected out and measured for radioactivity over a time course up to two hours. Major targets for administered leptin included the liver, kidneys, gastrointestinal tract and the skin while the lungs had high concentrations of administered leptin per gram of tissue. Leptin was also found to enter the lumen of the digestive tract intact from the plasma. Very little of the dose (<1 %) was recovered from the brain at any time. Consequently we confirm that the brain is not a major target for leptin from the periphery, although it may be very sensitive to leptin that does get to the hypothalamus. Several of the major targets (GI tract, skin and lungs) for leptin form the interface for the body with the environment, and given the ability of leptin to modulate immune function, this may represent a priming effect for tissues to respond to damage and infection., R. A. Hart, R. C. Dobos, L. L. Agnew, R. L. Tellam, J. R. McFarlane., and Obsahuje bibliografii

Language:

English

Rights:

http://creativecommons.org/publicdomain/mark/1.0/
policy:public

Source:

Physiological research | 2016 Volume:65 | Number:2

Harvested from:

CDK

Metadata only:

false