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題名 A possible correlation between oxytocin-induced and angiotensin IV-induced anti-hyperalgesia at the spinal level in rats
作者 Chow, Lok-Hi; Tao, Pao-Luh; Chen, Jin-Chun;Liao, Ruey-Ming; Chang, En-Pei; Huang, Eagle Yi-Kung; 廖瑞銘
貢獻者 國立政治大學心理學系
關鍵詞 Oxytocin; Angiotensin IV; Insulin-regulated aminopeptidase (IRAP); Hyperalgesia; Carrageenan; Spinal cord
日期 2013
上傳時間 29-Dec-2008 15:43:54 (UTC+8)
摘要 In our previous study, we showed that intrathecal (i.t.) administration of angiotensin IV (Ang IV), an insulin-regulated aminopeptidase (IRAP) inhibitor, attenuated inflammatory hyperalgesia in rats. Using the plantar test in rats with carrageenan-induced paw inflammation, we investigated the possible mechanism(s) of this effect. Because i.t. oxytocin was reported to produce a dose-dependent anti-hyperalgesia in rats with inflammation, we speculate that there is a possible correlation between oxytocin-induced and Ang IV-induced anti-hyperalgesia. Using i.t. co-administered atosiban (oxytocin receptor antagonist), the anti-hyperalgesia by Ang IV was completely abolished. This indicated that oxytocin could be the major IRAP substrate responsible for the anti-hyperalgesia by Ang IV. When Ang IV was co-administered with a low dose of oxytocin, there was a significant enhancing effect of Ang IV on oxytocin-induced anti-hyperalgesia. In recent reports, electrical stimulation on the paraventricular hypothalamic nucleus (PVN) was proved to increase oxytocin release at the spinal cord. Our results also showed that Ang IV could prolong the anti-hyperalgesia induced by PVN stimulation. This suggests a possible protective effect of Ang IV on endogenous oxytocin degradation/dysfunctioning. Moreover, we examined the local effect of intraplantarly injected Ang IV in the same model. Our results showed no effect of local Ang IV on hyperalgesia and paw edema, indicating that Ang IV may not regulate the peripheral inflammatory process. Overall, our study suggests that Ang IV may act through the inhibition of the activity of IRAP to reduce the degradation of oxytocin at the spinal cord, thereby leading to anti-hyperalgesia in rats with inflammation.
關聯 Peptides, 39(1), 21-28
資料類型 article
DOI http://dx.doi.org/10.1016/j.peptides.2012.10.012
dc.contributor 國立政治大學心理學系en_US
dc.creator (作者) Chow, Lok-Hi; Tao, Pao-Luh; Chen, Jin-Chun;Liao, Ruey-Ming; Chang, En-Pei; Huang, Eagle Yi-Kung; 廖瑞銘en_US
dc.date (日期) 2013en_US
dc.date.accessioned 29-Dec-2008 15:43:54 (UTC+8)-
dc.date.available 29-Dec-2008 15:43:54 (UTC+8)-
dc.date.issued (上傳時間) 29-Dec-2008 15:43:54 (UTC+8)-
dc.identifier.uri (URI) https://nccur.lib.nccu.edu.tw/handle/140.119/19979-
dc.description.abstract (摘要) In our previous study, we showed that intrathecal (i.t.) administration of angiotensin IV (Ang IV), an insulin-regulated aminopeptidase (IRAP) inhibitor, attenuated inflammatory hyperalgesia in rats. Using the plantar test in rats with carrageenan-induced paw inflammation, we investigated the possible mechanism(s) of this effect. Because i.t. oxytocin was reported to produce a dose-dependent anti-hyperalgesia in rats with inflammation, we speculate that there is a possible correlation between oxytocin-induced and Ang IV-induced anti-hyperalgesia. Using i.t. co-administered atosiban (oxytocin receptor antagonist), the anti-hyperalgesia by Ang IV was completely abolished. This indicated that oxytocin could be the major IRAP substrate responsible for the anti-hyperalgesia by Ang IV. When Ang IV was co-administered with a low dose of oxytocin, there was a significant enhancing effect of Ang IV on oxytocin-induced anti-hyperalgesia. In recent reports, electrical stimulation on the paraventricular hypothalamic nucleus (PVN) was proved to increase oxytocin release at the spinal cord. Our results also showed that Ang IV could prolong the anti-hyperalgesia induced by PVN stimulation. This suggests a possible protective effect of Ang IV on endogenous oxytocin degradation/dysfunctioning. Moreover, we examined the local effect of intraplantarly injected Ang IV in the same model. Our results showed no effect of local Ang IV on hyperalgesia and paw edema, indicating that Ang IV may not regulate the peripheral inflammatory process. Overall, our study suggests that Ang IV may act through the inhibition of the activity of IRAP to reduce the degradation of oxytocin at the spinal cord, thereby leading to anti-hyperalgesia in rats with inflammation.-
dc.format application/en_US
dc.language enen_US
dc.language en-USen_US
dc.language.iso en_US-
dc.relation (關聯) Peptides, 39(1), 21-28en_US
dc.subject (關鍵詞) Oxytocin; Angiotensin IV; Insulin-regulated aminopeptidase (IRAP); Hyperalgesia; Carrageenan; Spinal cord-
dc.title (題名) A possible correlation between oxytocin-induced and angiotensin IV-induced anti-hyperalgesia at the spinal level in ratsen_US
dc.type (資料類型) articleen
dc.identifier.doi (DOI) 10.1016/j.peptides.2012.10.012en_US
dc.doi.uri (DOI) http://dx.doi.org/10.1016/j.peptides.2012.10.012en_US