Preterm labour and resultant preterm birth are the most important problems
in perinatology. Countless efforts have failed to establish a single effect
ive treatment of preterm labour, partly because the mechanisms regulating t
he uterus and cervix during pregnancy are not well understood. New knowledg
e is needed to inhibit early progression of labour (uterine contractility a
nd cervical ripening), and adequate quantitative tools to evaluate the uter
us and cervix during pregnancy are lacking. In this review we outline studi
es showing that the uterus (myometrium) and cervix pass through a condition
ing step in preparation for labour. This step is not easily identifiable wi
th present methods to assess the uterus or cervix, In the uterus, this seem
ingly irreversible step consists of changes in the electrical properties to
make muscle more excitable and responsive to produce forceful contractions
, In the cervix, the step consists of softening of the connective tissue co
mponents, Progesterone appears to have a dominant role in controlling both
the uterus and cervix, as antiprogestins induce early, preterm conditioning
leading to preterm labour. Apparently, nitric oxide (NO) also controls con
ditioning of the uterus and cervix, Ire the uterus, NO, in concert with pro
gesterone, inhibits uterine contractility. At term, NO production by the ut
erus and placenta are decreased and allow labour to progress, in contrast?
NO in the cervix increases at the end of pregnancy and it may be the final
pathway for stimulating cervical ripening by activation of metalloenzymes,
The progress of labour can be assessed non-invasively using electromyograph
ic (EMG) signals front the uterus (the driving force for contractility) rec
orded from the abdominal surface. Uterine EMG bursts detected in this manne
r characterize uterine contractile events during human and animal pregnancy
. A low uterine EMG activity, measured transabdominally throughout most of
pregnancy, rises dramatically during labour. EMG activity also increases su
bstantially during preterm labour in humans and rats. This method may be us
ed one day to predict impending preterm labour sand identify control steps
and treatments. A quantitative method also assesses the cervix, using an op
tical device which measures collagen fluorescence in the cervix. The collas
cope estimates cervical collagen content from a fluorescent signal generate
d when collagen cross-links are illuminated with excitation light of about
340 mn, The system has proved useful in rats and humans at various stages o
f pregnancy, and indicates that cervical softening occurs progressively in
the last one-third of pregnancy. In rats, collascope readings correlate wit
h resistance measurements made in the isolated cervix, which may help to as
sess cervical function during pregnancy, and indicate control and treatment
s.