Subcellular distribution of somatostatin-14, somatostatin-28 and somatostatin-28(1–12) in rat brain cortex and comparisons of their respective binding sites in brain and pituitary

Subcellular distribution and binding characteristics of the three endogenous peptides somatostatin-14 (SRIF-14), somatostatin-28 (SRIF-28) and somatostatin-28(1–12) (SRIF-28(1–12)) derived from preprosomatostatin were investigated in the rat brain cortex. The three peptides are predominantly recovered from a crude mitochondrial pellet (P2), containing the pinched off nerve endings. Specific high affinity binding sites for 125 I-N- Tyr-SRIF-14 and 125 I-N- Tyr-SRIF-28 are present on pituitary and brain membranes. Under the same conditions, 125 I-N- Tyr-SRIF-28(1–12) binding is undetectable. Moreover, SRIF-28(1–12) does not displace 125 I-N- Tyr-SRIF-14 or 125 I-N- Tyr-SRIF-28 binding. SRIF-28 is more potent than SRIF-14 to displace 125 I-N- Tyr-SRIF-28 binding to brain and pituitary membranes, while both peptides are equipotent to displace 125 I-N- Tyr-SRIF-14 binding. Finally, the regional distribution of 125 I-N- Tyr-SRIF-14 and 125 I-N- Tyr-SRIF-28 binding sites in the brain is identical. In conclusion, the present results are consistent with a neurotransmitter and neurohormonal role for SRIF-14 and SRIF-28. The function of SRIF-28(1–12) in brain remains to be elucidated. Additionally, a differential role for SRIF-14 and SRIF-28 both in adenohypophysis and brain cannot be ascertained at the present time.