𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cerebral uptake of nicotine and of amino acids

✍ Scribed by Henry Sershen; Abel Lajtha


Publisher
John Wiley and Sons
Year
1979
Tongue
English
Weight
372 KB
Volume
4
Category
Article
ISSN
0360-4012

No coin nor oath required. For personal study only.

✦ Synopsis


Nicotine is among the compounds that enter the brain very rapidly (blood-flow-limited). It also leaves the brain rapidly; by five minutes, 90% exits, an exit somewhat slower than that of water. In spite of rapid exit, brain levels remain higher than levels in blood over a wide range of blood concentrations. Nicotine enters the fetal circulation from the maternal blood; it enters fetal brain but to a smaller extent than adult brain. Nicotine entry is different from that of amino acid: No interaction of amino acid transport and nicotine could be detected. Most close analogs have no effect on nicotine uptake, but at higher concentrations nicotine uptake is saturable. Nicotine and morphine mutually inhibit each other's uptake. The results suggest an uptake compartment (lipid space) for nicotine shared by morphine.


πŸ“œ SIMILAR VOLUMES


Cerebral uptake of amino acids in human
✍ Dr. William Sacks; Shirley Sacks; D. Robert Brebbia; Arthur Fleischer πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 English βš– 394 KB πŸ‘ 1 views

## Abstract In experiments with 11 human subjects and 12 rhesus monkeys given ^14^C‐labeled amino acids intravenously, blood samples were drawn simultaneously from the femoral artery (A) and the superior bulb of the internal jugular vein (V). Analyses of labeled and unlabeled free amino acids indic

Ethanol and amino acid uptake by hepatoc
✍ Mack C. Mitchell; Esteban Mezey πŸ“‚ Article πŸ“… 1987 πŸ› John Wiley and Sons 🌐 English βš– 344 KB πŸ‘ 1 views
Chemical stability, enzymatic hydrolysis
✍ Chun Yang; Hongwu Gao; Ashim K. Mitra πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 183 KB πŸ‘ 1 views

The objective of this work was to improve nasal absorption of relatively impermeable small drug molecules via an amino acid prodrug approach. Acyclovir was selected as a model drug. L-Aspartate beta-ester, L-lysyl, and L-phenylalanyl esters of acyclovir were synthesized to investigate their effectiv