CHAPTER 18
Hypothalamic Regulation of Hormonal Functions 277
OTHER FACTORS REGULATING
WATER INTAKE
A number of other well-established factors contribute to the
regulation of water intake. Psychologic and social factors are
important. Dryness of the pharyngeal mucous membrane
causes a sensation of thirst. Patients in whom fluid intake
must be restricted sometimes get appreciable relief of thirst by
sucking ice chips or a wet cloth.
Dehydrated dogs, cats, camels, and some other animals rapidly
drink just enough water to make up their water deficit. They stop
drinking before the water is absorbed (while their plasma is still
hypertonic), so some kind of pharyngeal gastrointestinal “meter-
ing” must be involved. Some evidence suggests that humans have
a similar metering ability, though it is not well developed.
CONTROL OF POSTERIOR
PITUITARY SECRETION
VASOPRESSIN & OXYTOCIN
In most mammals, the hormones secreted by the posterior pi-
tuitary gland are
arginine vasopressin (AVP)
and
oxytocin.
In hippopotami and most pigs, arginine in the vasopressin
molecule is replaced by lysine to form
lysine vasopressin.
The
posterior pituitaries of some species of pigs and marsupials
contain a mixture of arginine and lysine vasopressin. The pos-
terior lobe hormones are nonapeptides with a disulfide ring at
one end (Figure 18–5).
BIOSYNTHESIS, INTRANEURONAL
TRANSPORT, & SECRETION
The hormones of the posterior pituitary gland are synthesized
in the cell bodies of the magnocellular neurons in the supraoptic
and paraventricular nuclei and transported down the axons of
these neurons to their endings in the posterior lobe, where they
are secreted in response to electrical activity in the endings.
Some of the neurons make oxytocin and others make vaso-
pressin, and oxytocin-containing and vasopressin-containing
cells are found in both nuclei.
Oxytocin and vasopressin are typical
neural hormones,
that is, hormones secreted into the circulation by nerve cells.
This type of neural regulation is compared with other types in
Figure 18–6. The term
neurosecretion
was originally coined
to describe the secretion of hormones by neurons, but the
term is somewhat misleading because it appears that all neu-
rons secrete chemical messengers (see Chapter 7).
Like other peptide hormones, the posterior lobe hormones
are synthesized as part of larger precursor molecules. Vaso-
pressin and oxytocin each have a characteristic
neurophysin
associated with them in the granules in the neurons that
secrete them—neurophysin I in the case of oxytocin and neu-
rophysin II in the case of vasopressin. The neurophysins were
originally thought to be binding polypeptides, but it now
appears that they are simply parts of the precursor molecules.
The precursor for arginine vasopressin,
prepropressophysin,
contains a 19-amino-acid residue leader sequence followed by
FIGURE 18–5
Arginine vasopressin and oxytocin.
Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH 2
1 2 3 4 5 6 7 8 9
SS
Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH 2
1 2 3 4 5 6 7 8 9
SS
Arginine vasopressin
Oxytocin
FIGURE 18–6
Neural control mechanisms.
In the two situations on the left, neurotransmitters act at nerve endings on muscle; in the two
in the middle, neurotransmitters regulate the secretion of endocrine glands; and in the two on the right, neurons secrete hormones into the hy-
pophysial portal or general circulation.
Acetylcholine
Acetylcholine Acetylcholine Acetylcholine
Vasopressin
General
circulation
Norepinephrine
Epinephrine,
norepinephrine
ACTH, TSH,
GH, FSH, LH,
prolactin
Norepinephrine
or
acetylcholine
Releasing
and
inhibiting
hormones
Portal
vessels
Motor nerves
to skeletal
muscle
Motor nerves
to smooth and
cardiac muscle
Juxta-
glomerular
cells
Adrenal
medulla
Anterior
pituitary
Posterior
pituitary
Renin