Abstract:
:Neurotensin (NT) administered intracerebroventricularly (i.c.v.) to rats, blocks intestinal transit (tested by charcoal meal) in linear relation to the log of the doses within the range of 0.6-2.5 nmoles/rat. NT in this test is about 40 times more active than morphine (M) and 6 times less active than dermorphin (DM) on a molar basis. Within this dose range NT does not induce analgesia (tail-flick test) or hypothermia (tested at 22 degrees C). The intestinal effect can also be elicited by injecting the peptide into the periaqueductal gray matter (PAG). NT injected intraperitoneally (i.p.) is inactive up to doses 4 times the maximal active i.c.v. dose. Naloxone (Nx) and dynorphin 1-13 could not antagonize the intestinal effect of i.c.v. NT. The relationship between this central intestinal effect and many other central effects of NT is discussed.
journal_name
Life Scijournal_title
Life sciencesauthors
Parolaro D,Sala M,Crema G,Spazzi L,Gori Edoi
10.1016/0024-3205(83)90547-7subject
Has Abstractpub_date
1983-01-01 00:00:00pages
485-8eissn
0024-3205issn
1879-0631pii
0024-3205(83)90547-7journal_volume
33 Suppl 1pub_type
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