Alpha-melanocyte-stimulating hormone and behavior

• Published in: Neuroscience and biobehavioral reviews Vol. 6; no. 3; p. 297
• Main Authors: Datta, P C, King, M G
• Format: Journal Article
• Language: English
• Published: United States 01.01.1982
• Subjects: Adrenocorticotropic Hormone - physiology; Animals; Appetitive Behavior - physiology; Arousal - physiology; Attention - physiology; Avoidance Learning - physiology; Behavior, Animal - physiology; Brain - physiology; Chemical Phenomena; Chemistry; Discrimination Learning - physiology; Electroencephalography; Evoked Potentials; Humans; Hypothalamo-Hypophyseal System - physiology; Melanocyte-Stimulating Hormones - physiology; Mental Recall - physiology; Pineal Gland - physiology; Synaptic Transmission
• DOI: 10.1016/0149-7634(82)90042-2
• ISSN: 0149-7634

Melanocyte-stimulating hormone (MSH) has putative adaptive significance in all forms of species where it is present. In mammals the polypeptide chain influences learning, memory and attention. Chemically MSH shares the first 13 (alpha-MSH) or the first 18 or 22 (beta-MSH) amino acids with adrenocorticotropic hormone (ACTH), even though the mechanisms of secretion and behavioral effects are often quite different. The still shorter peptide chain MSH/ACH4-10 demonstrates significant melanotropic and behavioral actions of alpha-MSH without showing any steroidogenic effect. Behaviorally, alpha-MSH and MSH/ACTH analogues (MSH/ACTH4-9 and MSH/ACTH4-10 influence the parameters of learning, attention and memory in both human and infrahuman subjects. Alpha-MSH has also been reported to increase sensitivity and augment arousal mechanisms in the CNS. Alpha-MSH has been observed to increase and sustain novelty-induced defecation, and this behavior was found to be accompanied by a concomitant decrease in whole brain DA and NE levels in both intact and hypophysectomized rats exposed daily to a test box. The behavioral effects of alpha-MSH may be partially modulated by the enhanced cyclic-AMP activity in the CNS observed after MSH administration. MSH also seems to be working in conjunction with the hypothalamic tripeptide MIF-1 and the pineal hormone melatonin, both of which can affect the release of MSH from the pituitary. Recent evidence suggests that MSH is counterbalancing against and complementing with the effects of endorphins, specifically beta-endorphin (61-91 chain of beta-LPH), in maintaining learning and attentive behaviors.