Effect of oily vehicles on absorption of mepitiostane by the lymphatic system in rats. 1992

T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
Shionogi Research Laboratories, Shionogi & Co. Ltd, Osaka, Japan.

[14C]Mepitiostane in various vehicles was administered to the small intestine of anaesthetized rats with cannulated thoracic ducts, and the effect of lipids on lymphatic absorption was examined. The extent of lymphatic absorption was greatest when administered in triolein and sesame oil, which are triglycerides of long-chain fatty acids. Absorption in the presence of other vehicles was in the order of 10% Tween 80 aqueous solution greater than monolein greater than oleic acid approximately oleic acid/monolein (2:1 mol/mol) greater than aqueous suspension. Differences between the extents of lymphatic absorption of mepitiostane in the various formulations were not due to variation in the lymph flow but to the increased secretion of chylomicron and very low density lipoproteins. During absorption of mepitiostane from the small intestine, oil affected not only the penetration into epithelium cells and the metabolism in them, but also the partition between blood and lymph.

UI MeSH Term Description Entries
D007408 Intestinal Absorption Uptake of substances through the lining of the INTESTINES. Absorption, Intestinal
D007421 Intestine, Small The portion of the GASTROINTESTINAL TRACT between the PYLORUS of the STOMACH and the ILEOCECAL VALVE of the LARGE INTESTINE. It is divisible into three portions: the DUODENUM, the JEJUNUM, and the ILEUM. Small Intestine,Intestines, Small,Small Intestines
D008196 Lymph The interstitial fluid that is in the LYMPHATIC SYSTEM. Lymphs
D008208 Lymphatic System A system of organs and tissues that process and transport immune cells and LYMPH. Lymphatic Systems
D009821 Oils Unctuous combustible substances that are liquid or easily liquefiable on warming, and are soluble in ether but insoluble in water. Such substances, depending on their origin, are classified as animal, mineral, or vegetable oils. Depending on their behavior on heating, they are volatile or fixed. (Dorland, 28th ed)
D011919 Rats, Inbred Strains Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations or by parent x offspring matings carried out with certain restrictions. This also includes animals with a long history of closed colony breeding. August Rats,Inbred Rat Strains,Inbred Strain of Rat,Inbred Strain of Rats,Inbred Strains of Rats,Rat, Inbred Strain,August Rat,Inbred Rat Strain,Inbred Strain Rat,Inbred Strain Rats,Inbred Strains Rat,Inbred Strains Rats,Rat Inbred Strain,Rat Inbred Strains,Rat Strain, Inbred,Rat Strains, Inbred,Rat, August,Rat, Inbred Strains,Rats Inbred Strain,Rats Inbred Strains,Rats, August,Rats, Inbred Strain,Strain Rat, Inbred,Strain Rats, Inbred,Strain, Inbred Rat,Strains, Inbred Rat
D002250 Carbon Radioisotopes Unstable isotopes of carbon that decay or disintegrate emitting radiation. C atoms with atomic weights 10, 11, and 14-16 are radioactive carbon isotopes. Radioisotopes, Carbon
D004337 Drug Carriers Forms to which substances are incorporated to improve the delivery and the effectiveness of drugs. Drug carriers are used in drug-delivery systems such as the controlled-release technology to prolong in vivo drug actions, decrease drug metabolism, and reduce drug toxicity. Carriers are also used in designs to increase the effectiveness of drug delivery to the target sites of pharmacological actions. Liposomes, albumin microspheres, soluble synthetic polymers, DNA complexes, protein-drug conjugates, and carrier erythrocytes among others have been employed as biodegradable drug carriers. Drug Carrier
D005260 Female Females
D000732 Androstanols Androstanes and androstane derivatives which are substituted in any position with one or more hydroxyl groups. Hydroxyandrostanes

Related Publications

T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
August 1976, Chemical & pharmaceutical bulletin,
T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
January 1957, Archivio italiano di scienze farmacologiche,
T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
March 1975, Journal of pharmaceutical sciences,
T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
July 1956, Archivio italiano di scienze farmacologiche,
T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
January 1990, Comparative biochemistry and physiology. A, Comparative physiology,
T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
January 1987, The Journal of pharmacy and pharmacology,
T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
July 1977, Chemical & pharmaceutical bulletin,
T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
October 1981, Journal of pharmaceutical sciences,
T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
May 1984, Journal of pharmacobio-dynamics,
T Ichihashi, and H Kinoshita, and Y Takagishi, and H Yamada
October 1980, Veterinary and human toxicology,
Copied contents to your clipboard!