Oral morphine induces spinal 5‐hydroxytryptamine (5‐HT) release using an opioid receptor‐independent mechanism

Abstract Morphine induces spinal 5‐hydroxytryptamine (5‐HT) release, but the role and mechanism of the spinal 5‐HT release induced by morphine are not well understood. The purpose of this study was to define the role and mechanism of spinal 5‐HT release induced by oral morphine. We also examined whe...

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প্রধান লেখক: Shingo Nakamura (Author), Shuji Komatsu (Author), Toshihiko Yamada (Author), Hiromi Kitahara (Author), Tatsuo Yamamoto (Author)
বিন্যাস: গ্রন্থ
প্রকাশিত: Wiley, 2023-08-01T00:00:00Z.
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LEADER 00000 am a22000003u 4500
001 doaj_3e470ae229a149eb954b18a63a1dba3a
042 |a dc 
100 1 0 |a Shingo Nakamura  |e author 
700 1 0 |a Shuji Komatsu  |e author 
700 1 0 |a Toshihiko Yamada  |e author 
700 1 0 |a Hiromi Kitahara  |e author 
700 1 0 |a Tatsuo Yamamoto  |e author 
245 0 0 |a Oral morphine induces spinal 5‐hydroxytryptamine (5‐HT) release using an opioid receptor‐independent mechanism 
260 |b Wiley,   |c 2023-08-01T00:00:00Z. 
500 |a 2052-1707 
500 |a 10.1002/prp2.1119 
520 |a Abstract Morphine induces spinal 5‐hydroxytryptamine (5‐HT) release, but the role and mechanism of the spinal 5‐HT release induced by morphine are not well understood. The purpose of this study was to define the role and mechanism of spinal 5‐HT release induced by oral morphine. We also examined whether persistent pain affected the spinal 5‐HT release induced by oral morphine. Spinal 5‐HT release was measured using microdialysis of lumbar cerebrospinal fluid (CSF). Two opioids, morphine and oxycodone, were orally administered and 5‐HT release was measured in awake rats. Naloxone and β‐funaltrexamine (β‐FNA) were used to determine whether the effect of morphine on 5‐HT release was mediated by opioid receptor activation. To study persistent pain, a formalin test was used. At 45 min after oral morphine administration, the formalin test was started and spinal 5‐HT release was measured. Oral morphine, but not oral oxycodone, increased 5‐HT release at the spinal cord to approximately 4000% of the baseline value. This effect of morphine was not antagonized by either naloxone or β‐FNA at a dose that antagonized the antinociceptive effect of morphine. Formalin‐induced persistent pain itself had no effect on spinal 5‐HT release but enhanced the oral morphine‐induced spinal 5‐HT release. Oral morphine‐induced spinal 5‐HT release was not mediated by opioid receptor activation. Spinal 5‐HT induced by oral morphine did not play a major role in the antinociceptive effect of morphine in the hot plate test. Persistent pain increased oral morphine‐induced spinal 5‐HT release. 
546 |a EN 
690 |a 5‐HT 
690 |a antinociception 
690 |a morphine 
690 |a oxycodone 
690 |a persistent pain 
690 |a spinal cord 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Pharmacology Research & Perspectives, Vol 11, Iss 4, Pp n/a-n/a (2023) 
787 0 |n https://doi.org/10.1002/prp2.1119 
787 0 |n https://doaj.org/toc/2052-1707 
856 4 1 |u https://doaj.org/article/3e470ae229a149eb954b18a63a1dba3a  |z Connect to this object online.