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Vol. 28, Issue 9, 1038-1042, September 2000
Division of Pharmaceutical Sciences, School of Pharmacy, University
of Missouri, Kansas City, Missouri
Tryptophan hydroxylase (TrpH) catalyzes a rate-limiting step
in the biogenesis of serotonin. The main objective of this study is to
investigate the effect of aging on the activity of TrpH in
serotonergic-enriched brain regions such as midbrain, pons, and
medulla. TrpH activity was monitored by incubating various concentrations of tryptophan in a fixed amount of brain homogenate from
midbrain, pons, and medulla of 2-month (young), 12-month (mature), and
24-month (old) rats (pH 7.4, 37°C). The product 5-hydroxytryptophan
was quantitated using a reversed phase HPLC equipped with an
electrochemical detection system. Michaelis-Menton constants,
Km and Vmax, were
calculated using the Lineweaver-Burk plot. The affinity
(Km) of the enzyme significantly declined in midbrain and pons of old rats (141.1 ± 2.6, 126.0 ± 10.8 µM) relative to mature rats (22.4 ± 7.7, 38.2 ± 4.7 µM). However, no change was observed in medulla of old rats. The
Vmax of TrpH in pons of all three age group
rats was fairly constant. However, the Vmax
of midbrain was significantly elevated, whereas that of medulla was
reduced in old rats relative to mature rats. Clearance formation, a
ratio of Vmax to
Km, of 5-hydroxytryptophan declined
significantly in midbrain, pons, and medulla of old rats relative to
mature rats. A combined effect of inefficient phosphorylation and
oxidative damage of TrpH enzyme may be responsible for lower TrpH
activity in aging brain. Such alterations in TrpH activity may reduce
the level of serotonin in brain, which may be linked to late-life depression and other brain disorders, such as Alzheimer and Parkinson diseases.