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Transport of pipecolic acid in adult and developing mouse brain.

作者信息

Kim J S, Giacobini E

出版信息

Neurochem Res. 1985 Oct;10(10):1405-15. doi: 10.1007/BF00964981.

DOI:10.1007/BF00964981
PMID:4069310
Abstract

In an effort to develop an animal model of hyperpipecolatemia, the uptake of pipecolic acid (PA) in the brain and changes of PA levels in serum following administration of D,L-PA were studied in the mouse using a new sensitive HPLC-EC method. Following i.p. injections (250 mg/kg) to adult male mice, the brain concentration peaks at 5-10 min (40 nmol/g). The level remains relatively stable up to 5 hrs and then declines slowly to 24 hrs. In serum, the level of PA increases rapidly to reach the maximum value at 10 min and then decreases rapidly in the first hour and continues to decline more slowly to 24 hrs. The net uptake of PA following administration of various amounts of D,L-PA is saturable at low doses (3.9-15.6 mg/kg), and it increases linearly at higher doses in a dose-dependent manner up to the maximum dose (500 mg/kg) used in the present study. Kinetic analysis suggests the presence of two kinds of transport systems. These findings are in good agreement with the previous results using D,L-[3H]PA in the mouse (7) and L-[14C]PA in the rat (13). There were no significant differences between uptake of D-pipecolic acid and L-pipecolic acid (250 mg/kg, i.p., 10 min), suggesting the absence of stereospecificity for PA uptake in the mouse brain. Developmental changes in net brain uptake of PA following injections of D,L-PA (250 mg/kg, s.c., 10 min) showed an age-dependent decrease which continues until adult levels are reached at four weeks after birth. The results suggest that the blood brain barrier (BBB) for PA is completed during the first month of life. Following administration of D,L-PA (250 mg/kg, s.c.) to pregnant mice during the period 19-21 days of gestation, PA level increases in fetal brain to a maximum value at 2 hrs (420 nmol/g). This level is unchanged during 24 hrs. The maximum level of PA in fetal serum is reached at 30 min to 1 hr. The level gradually decreases after 1 hr over 24 hrs. These results indicate that PA taken up by the placenta and into the brain is transported from the fetal circulation.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

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1
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本文引用的文献

1
The conversion of lysine into piperidine, cadaverine, and pipecolic acid in the brain and other organs of the mouse.赖氨酸在小鼠脑和其他器官中转化为哌啶、尸胺和哌可酸。
Neurochem Res. 1977 Dec;2(6):619-37. doi: 10.1007/BF00963776.
2
Accumulation and metabolism of pipecolic acid in the brain and other organs of the mouse.小鼠大脑及其他器官中哌啶酸的积累与代谢。
Neurochem Res. 1981 Dec;6(12):1241-52. doi: 10.1007/BF00964346.
3
Metabolism and uptake of L-pipecolic acid by brain and heart.
Life Sci. 1981 Aug 31;29(9):947-54. doi: 10.1016/0024-3205(81)90397-0.
4
The effects of hyperphenylalaninemia on fetal development: a new animal model of maternal phenylketonuria.
Pediatr Res. 1982 May;16(5):388-94. doi: 10.1203/00006450-198205000-00014.
5
Developmental modulations of blood-brain barrier permeability as an indicator of changing nutritional requirements in the brain.血脑屏障通透性的发育调节作为大脑营养需求变化的指标。
Pediatr Res. 1982 Apr;16(4 Pt 1):324-8. doi: 10.1203/00006450-198204000-00017.
6
Accumulation and metabolism of pipecolic acid in the developing brain of the mouse.小鼠发育大脑中哌啶酸的积累与代谢
Brain Res. 1983 Jan;282(2):107-12. doi: 10.1016/0165-3806(83)90088-3.
7
Hyperpipecolic acidemia. Occurrence in an infant with clinical findings of the cerebrohepatorenal (Zellweger) syndrome.高哌可酸血症。在一名患有脑肝肾(泽尔韦格)综合征临床表现的婴儿中的发生情况。
Arch Neurol. 1982 Nov;39(11):713-6. doi: 10.1001/archneur.1982.00510230039011.
8
Brain uptake of pipecolic acid, amino acids, amines following intracarotid injection in the mouse.小鼠颈内注射后,脑对哌啶酸、氨基酸、胺的摄取情况。
Neurochem Res. 1981 Aug;6(8):835-45. doi: 10.1007/BF00965042.
9
Pipecolic acid: origin, biosynthesis and metabolism in the brain.哌啶酸:在大脑中的起源、生物合成及代谢
Cell Mol Biol Incl Cyto Enzymol. 1980;26(2):135-46.
10
Blood-brain barrier transport of L-pipecolic acid in various rat brain regions.
Neurochem Res. 1983 Sep;8(9):1087-96. doi: 10.1007/BF00964924.