Effects of pregnancy and delivery on the availability of plasma tryptophanto the brain: relationships to delivery-induced immune activation and early post-partum anxiety and depression
M. Maes et al., Effects of pregnancy and delivery on the availability of plasma tryptophanto the brain: relationships to delivery-induced immune activation and early post-partum anxiety and depression, PSYCHOL MED, 31(5), 2001, pp. 847-858
Background. There is now evidence that the availability of plasma tryptopha
n is decreased during pregnancy and the puerperium and also in patients wit
h major depression and inflammation. The aims of the present study were to
examine: (i) the effects of pregnancy and delivery on plasma tryptophan and
the amino acids known to compete for the same cerebral uptake mechanism (C
AAs), valine, leucine, tyrosine, phenylalanine and isoleucine; (ii) the rel
ationships between the availability of plasma tryptophan and postpartum dep
ression or anxiety; and (iii) the relationships between the availability of
plasma tryptophan to the brain and inflammatory markers, such as serum int
erleukin-6 (IL-6), interleukin-1 receptor-antagonist (IL-1RA) and the leuka
emia inhibitory factor receptor (LIF-R).
Methods. The above variables were measured in 13 healthy non-pregnant and i
n 98 pregnant women 3 to 6 days before delivery and 1 and 3 days after deli
very. On each occasion the parturient women completed the state version of
Spielberger State-Trait Anxiety Inventory (STAI) and the Zung Depression Ra
ting Scale (ZDS).
Results. Plasma tryptophan and the tryptophan/CAA ratio were significantly
lower at the end of term and after delivery than in the plasma of non-pregn
ant, healthy women. The tryptophan/CAA ratio was significantly lower in the
early puerperium than at the end of term. There were no significant relati
onships between the availability of plasma tryptophan and either post-partu
m depression or changes in the STAI or ZDS scores in the early puerperium.
The changes in the tryptophan/CAA ratio from the end of term to the early p
uerperium were significantly and inversely related to serum IL-6, IL-1RA an
d LIF-R.
Conclusions. The results show that the reduction in the availability of pla
sma tryptophan from the end of term to the early puerperium is related to i
mmune activation: and that the lowered availability of plasma tryptophan is
not related either to depressive or anxiety symptoms in the early puerperi
um or to post-partum depression ensuing some months later.