Secretion of steroid hormones by the adrenal cortex is required to mai
ntain whole body homeostasis; that is the ability to maintain blood pr
essure and volume, carbohydrate, protein and fat metabolism and immune
and nervous system function within normal limits is dependent on adre
nocortical hormones. The premise of this report is that autonomic-endo
crine interactions occurring in the adrenal cortex are required for no
rmal control of steroid secretion. Under non-stress conditions when re
duced steroid secretion is required, splanchnic neural activity appear
s to be inhibitory, whereas during stress conditions when elevated ste
roid secretion is necessary, neural activity is excitatory. The capaci
ty for innervation to produce both inhibitory and excitatory effects s
uggests that neural input must be encoded differentially; encoding cou
ld be dependent on the neurotransmitter released or on the intra-adren
al target affected. Neural input could act directly at the adrenal cel
l to affect steroidogenesis or act indirectly by changing adrenal bloo
d flow. An index of the role of innervation has been obtained by asses
sing adrenal corticosteroid secretion after splanchnicectomy, severing
the thoracic splanchnic nerve which is the major source of innervatio
n of the adrenal gland. This approach has resulted in alterations in c
orticosteroid secretion under nonstress and stress conditions, but in
many cases has demonstrated no profound effect on in vivo steroidogene
sis. It is likely that splanchnicectomy results in variable secretory
responses in part due to the multiplicity of adrenal neurotransmitter
systems that are regulated by the splanchnic nerve. Splanchnicectomy a
lters multiple neurotransmitters at different adrenal sites. Splanchni
c innervation acts as an extra-ACTH mechanism in the control of adrena
l corticosteroid secretion, yet further elucidation of the physiologic
al conditions under which splanchnic neural activity affects function
is clearly warranted.