Pregled bibliografske jedinice broj: 33465
Nociception and brain serotonin following single intraperitoneal injection and long lasting peroral glucose intake in rats
Nociception and brain serotonin following single intraperitoneal injection and long lasting peroral glucose intake in rats // Naunyn-Schmiedberg's Archiver of Pharmacology XIIIth International Congress of Pharmacology / Gothert, M ; Jakobs KH (ur.).
Berlin: Springer, 1998. str. R79-R79 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
Nociception and brain serotonin following single intraperitoneal injection and long lasting peroral glucose intake in rats
Autori
Šalković-Petrišić, Melita ; Bonassin, Corrado ; Lacković, Zdravko
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Naunyn-Schmiedberg's Archiver of Pharmacology
XIIIth International Congress of Pharmacology
/ Gothert, M ; Jakobs KH - Berlin : Springer, 1998, R79-R79
Skup
XIIIth International Congress of Pharmacology
Mjesto i datum
München, Njemačka, 26.07.1998. - 31.07.1998
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
glucose; brain serotonin; nociception
Sažetak
The influence of elevated glucose intake on nociception has been investigated mostly in hyperglycemic, diabetic rats or in healthy rats fey hours following a single glucose application. We have investigated the time (up to 4 weeks) and the dose (0.1-1 M) response of a single intraperitoneal /i.p./ injection of glucose and the influence of 1 week lasting peroral /p.o./ 0.2 M glucose on nociception in healthy rats. Pain threshold has been determined as the tail flick latency in tail immersion test at the 55 *C. Brain serotonin (5-HT) and its metabolite, 5-hydroxyindoleacetic acid (5-HIAA) have been measured spectrophotofluorimetrically. Following a single i.p. injection of 0.2M glucose pain threshold rises and remains elevated up to 3 weeks posttreatment (20-70%), with an increase being dose dependent at the 2nd and 7th day following 0.2, 0.5 and 1M glucose i.p. injection 832-83%), respectively. Increased pain threshold has also been found at the 1st (79%) and 7th day (43%) following the continuous p.o. intake of 0.2M glucose. In rats kept on 0.M glucose p.o. intake for 7 days the content of brain 5-HT, possible modulator of nociception is decreased (-33%), while the 5-HIAA content is increased (20%). 7 days following single i.p. injection of 0.2M glucose the content of brain 5-HIAA is increased (19%), as well. Unchanged or mildly decreased blood glucose levels in glucose treated animals suggest that altered nociception may be related to glucose-induced insulin secretion and/or altered brain 5-HT transmission, at least in long lasting glucose p.o. treated rats.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti