1988
DOI: 10.1016/0024-3205(88)90296-2
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Intragastric administration of cyclo(Leu-Gly) inhibits the development of tolerance to the analgesic effect of morphine in the rat

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Cited by 29 publications
(3 citation statements)
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“…The tripeptide Pro-Leu-Gly-NH 2 (MiF-1, MSH release-inhibiting factor) given once a day (1 mg/kg) alters the development of opiate tolerance (delayed tolerance to the analgesic action of morphine; Kastin et al 1979). The MIF-1 derivative cyclo (Leu-Gly) exerts the same activity even after intragastric administration (Bhargava 1988). All these findings suggest that several peptides and opiates administered outside the central nervous system (CNS) interact with regulatory processes in the CNS by influencing peripheral, sites and by transmitting information via afferent neurones.…”
Section: Km Important Afferent Ayfonomic Reflexes Input Akira Niijimamentioning
confidence: 99%
“…The tripeptide Pro-Leu-Gly-NH 2 (MiF-1, MSH release-inhibiting factor) given once a day (1 mg/kg) alters the development of opiate tolerance (delayed tolerance to the analgesic action of morphine; Kastin et al 1979). The MIF-1 derivative cyclo (Leu-Gly) exerts the same activity even after intragastric administration (Bhargava 1988). All these findings suggest that several peptides and opiates administered outside the central nervous system (CNS) interact with regulatory processes in the CNS by influencing peripheral, sites and by transmitting information via afferent neurones.…”
Section: Km Important Afferent Ayfonomic Reflexes Input Akira Niijimamentioning
confidence: 99%
“…In addition, cyclo‐His‐Pro showed anti‐inflammatory effect by suppressing pro‐inflammatory necrosis factor (NF)‐ κ B signalling via Nrf2‐mediated hemeoxygenase‐1 activation . While others cyclic dipeptides containing glycine, as cyclo‐Leu‐Gly, have been studied extensively aiming toward the development of therapeutic agents for inhibit opiate‐induced tolerance …”
Section: Introductionmentioning
confidence: 99%
“…15 While others cyclic dipeptides containing glycine, as cyclo-Leu-Gly, have been studied extensively aiming toward the development of therapeutic agents for inhibit opiate-induced tolerance. 16 The cyclo-Gly-Pro peptide is naturally derived from the Nterminus of the insulin-like growth factor-1 (IGF-1). 17 Some beneficial activities, such as memory enhancement 12 and neuroprotection after ischemic brain injury, 18 have been attributed to cyclo-Gly-Pro.…”
Section: Introductionmentioning
confidence: 99%