Ca. Loretz, INHIBITION OF GOBY POSTERIOR INTESTINAL NACL ABSORPTION BY NATRIURETIC PEPTIDES AND BY CARDIAC EXTRACTS, Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology, 166(8), 1996, pp. 484-491
Natriuretic peptides abolish active Na+ and Cl- absorption across the
posterior intestine of the euryhaline goby Gillichthys mirabilis. Inhi
bition by eel and human natriuretic peptides is dose-dependent with th
e following sequence of potencies based on experimentally determined I
D50 values for inhibition of short-circuit current: eel ventricular na
triuretic peptide (78 nmol . 1(-1)), eel atrial natriuretic peptide (1
56 nmol . 1(-1)), human brain natriuretic peptide (326 nmol . 1(-1)),
human alpha atrial natriuretic peptide (1.05 mu mol . 1(-1)), and eel
C-type natriuretic peptide (75 mu mol . 1(-1)). Natriuretic peptides a
lso significantly increase transcellular conductance. The observed seq
uence of natriuretic peptide potencies is suggestive of cellular media
tion by GC-A-type NP-R(1) receptors in this tissue, as expected for gu
anylyl-cyclase-coupled NP-R(1) receptors, cyclic GMP mimics the action
of natriuretic peptides on the goby intestine. Crude aqueous extracts
of goby atrium and ventricle inhibited short circuit current and incr
eased tissue conductance in a dose-dependent manner. Ventricular extra
ct was more potent than atrial extract on both a pei organ and per mil
ligram basis.