TREATMENT OF GROWTH HORMONE-DEFICIENT ADULTS WITH RECOMBINANT HUMAN GROWTH-HORMONE INCREASES THE CONCENTRATION OF GROWTH-HORMONE IN THE CEREBROSPINAL-FLUID AND AFFECTS NEUROTRANSMITTERS
Jo. Johansson et al., TREATMENT OF GROWTH HORMONE-DEFICIENT ADULTS WITH RECOMBINANT HUMAN GROWTH-HORMONE INCREASES THE CONCENTRATION OF GROWTH-HORMONE IN THE CEREBROSPINAL-FLUID AND AFFECTS NEUROTRANSMITTERS, Neuroendocrinology, 61(1), 1995, pp. 57-66
In a double-blind, placebo-controlled trial, the effects of recombinan
t human growth hormone were studied on cerebrospinal fluid concentrati
ons of growth hormone, insulin-like growth factor 1 (IGF-1), insulin-l
ike growth factor binding protein-3 (IGFBP-3), monoamine metabolites,
neuropeptides and endogenous opioid peptides. Twenty patients, 10 pati
ents in each of 2 groups, with adult-onset, growth hormone deficiency
were treated for 1 month with recombinant human growth hormone (0.25 U
/kg/week) or placebo. All the patients received the appropriate thyroi
d, adrenal and gonadal hormone replacement. In cerebrospinal fluid, th
e mean concentration of growth hormone increased from 13.3 +/- 4.4 to
149.3 +/- 22.2 mu U/l (p = 0.002), during recombinant human growth hor
mone treatment. The cerebrospinal fluid IGF-1 concentration increased
from 0.67 +/- 0.04 to 0.99 +/- 0.10 mu g/l(p = 0.005) and the IGFBP-3
concentration rose from 13.4 +/- 1.25 to 17.5 +/- 1.83 mu g/l (p = 0.0
02). The dopamine metabolite homovanillic acid decreased from 282.1 +/
- 36.0 to 234.3 +/- 26.5 nmol/l (p = 0.02) and the vasoactive intestin
al peptide decreased from 4.1 +/- 0.6 to 3.7 +/- 0.4 pmol/l (p = 0.03)
. Cerebrospinal fluid immunoreactive beta-endorphin increased from 24.
4 +/- 1.8 to 29.9 +/- 2.1 pmol/l (p = 0.002). There were no significan
t changes compared to baseline in the cerebrospinal fluid concentratio
ns of enkephalins, dynorphin A, the norepinephrine metabolite 3-methox
y-4-hydroxyphenyl-ethyleneglycol, the serotonin metabolite 5-hydroxyin
doleacetic acid, gamma-aminobutyric acid, somatostatin or corticotropi
n-releasing factor. We conclude that treatment with recombinat human g
rowth hormone causes a tenfold increase in growth hormone in the cereb
rospinal fluid, thereby indicating that recombinant human growth hormo
ne passes the blood-cerebrospinal fluid barrier. The cerebrospinal flu
id concentrations of IGF-1 and IGFBP-3 increased significantly. Simult
aneously, the cerebrospinal fluid concentrations of homovanillic acid
and vasoactive intestinal peptide decreased and the concentration of b
eta-endorphin immunoreactivities increased significantly. These change
s,might explain the improved quality-of-life in patients with growth h
ormone deficiency following replacement therapy with growth hormone.