Literature DB >> 15183523

Altered pain-related behaviors and spinal neuronal responses produced by s.c. injection of melittin in rats.

K-C Li1, J Chen.   

Abstract

Recently, we have reported that following s.c. injection of a solution containing the whole bee-venom (BV; Apis mellifera), into one hind paw of a rat, the experimentally produced honeybee's sting, the animal shows altered pain-related behaviors and inflammation relevant to pathological pain state. To see whether melittin, the major (over 50%) toxic component of the BV, is responsible for the above abnormal pain behavioral changes, the present study was designed to investigate the effects of s.c. melittin on either nociceptive behaviors in conscious rats or spinal dorsal horn neuronal responses in anesthetized rats. In the behavioral surveys, s.c. injection of three doses of both melittin (5, 25 and 50 microg) and BV (10, 50 and 100 microg) into the posterior surface of one hind paw of rats produced an immediate tonic nociceptive response displaying as persistent spontaneous paw flinching reflex. Similar to the BV test, the melittin response was also monophasic and dose-dependent in terms of both intensity and time course. As an accompanied consequence, both heat and mechanical hypersensitivity (hyperalgesia and allodynia) and inflammatory responses (paw swelling and plasma extravasation) were induced by s.c. melittin injections. In the electrophysiological recordings, s.c. injection of the same three doses of melittin into the cutaneous receptive field produced an immediate, dose-dependent increase in spontaneous spike discharges of spinal dorsal horn wide-dynamic-range (WDR) neurons which are believed to be responsible for the spinally-organized nociceptive flexion reflex. The melittin-induced ongoing spike responses are similar to the behavioral flinching reflex in terms of both duration and frequency. Furthermore, the responsiveness of the WDR neurons to both heat (42 degrees C, 45 degrees C, 47 degrees C and 49 degrees C) and mechanical (brush, pressure and pinch) stimuli was significantly enhanced by s.c. injection of melittin shown as a leftward shift of the stimulus-response functional curves. Taken together, the present results suggest that melittin, the major toxin of the whole BV, is likely to be responsible for production of the long-term spinal neuronal changes as well as persistent spontaneous nociception, heat/mechanical hypersensitivity and inflammatory responses that are produced by experimental honeybee's sting.

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Year:  2004        PMID: 15183523     DOI: 10.1016/j.neuroscience.2004.03.050

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  19 in total

1.  Melittin activates TRPV1 receptors in primary nociceptive sensory neurons via the phospholipase A2 cascade pathways.

Authors:  Yi-Ru Du; Yong Xiao; Zhuo-Min Lu; Jing Ding; Fang Xie; Han Fu; Yan Wang; Judith A Strong; Jun-Ming Zhang; Jun Chen
Journal:  Biochem Biophys Res Commun       Date:  2011-03-29       Impact factor: 3.575

2.  Involvement of peripheral NMDA receptor in melittin-induced thermographic flare.

Authors:  Narihito Iwashita; Shuichi Nosaka; Natsu Koyama
Journal:  Neurochem Res       Date:  2012-08-01       Impact factor: 3.996

3.  Spatial and temporal plasticity of synaptic organization in anterior cingulate cortex following peripheral inflammatory pain: multi-electrode array recordings in rats.

Authors:  Yun-Fei Lu; Yan Wang; Ying He; Fu-Kang Zhang; Ting He; Rui-Rui Wang; Xue-Feng Chen; Fei Yang; Ke-Rui Gong; Jun Chen
Journal:  Neurosci Bull       Date:  2013-05-18       Impact factor: 5.203

4.  Effects of SKF-96365, a TRPC inhibitor, on melittin-induced inward current and intracellular Ca2+ rise in primary sensory cells.

Authors:  Jing Ding; Yong Xiao; Dan Lu; Yi-Ru DU; Xiu-Yu Cui; Jun Chen
Journal:  Neurosci Bull       Date:  2011-06       Impact factor: 5.203

Review 5.  Melittin, the Major Pain-Producing Substance of Bee Venom.

Authors:  Jun Chen; Su-Min Guan; Wei Sun; Han Fu
Journal:  Neurosci Bull       Date:  2016-03-17       Impact factor: 5.203

6.  Involvement of Rac1 signalling pathway in the development and maintenance of acute inflammatory pain induced by bee venom injection.

Authors:  Yan Wang; Yun-Fei Lu; Chun-Li Li; Wei Sun; Zhen Li; Rui-Rui Wang; Ting He; Fan Yang; Yan Yang; Xiao-Liang Wang; Su-Min Guan; Jun Chen
Journal:  Br J Pharmacol       Date:  2016-02-10       Impact factor: 8.739

7.  Effects of a non-selective TRPC channel blocker, SKF-96365, on melittin-induced spontaneous persistent nociception and inflammatory pain hypersensitivity.

Authors:  Jing Ding; Jia-Rui Zhang; Yan Wang; Chun-Li Li; Dan Lu; Su-Min Guan; Jun Chen
Journal:  Neurosci Bull       Date:  2012-04       Impact factor: 5.203

8.  Spinal Metabotropic Glutamate Receptors (mGluRs) are Involved in the Melittin-induced Nociception in Rats.

Authors:  Chul Hyun Cho; Hong Kee Shin
Journal:  Korean J Physiol Pharmacol       Date:  2008-10-31       Impact factor: 2.016

9.  Distinct contributions of reactive oxygen species in amygdala to bee venom-induced spontaneous pain-related behaviors.

Authors:  Yun-Fei Lu; Volker Neugebauer; Jun Chen; Zhen Li
Journal:  Neurosci Lett       Date:  2016-03-10       Impact factor: 3.046

10.  Roles of peripheral P2X and P2Y receptors in the development of melittin-induced nociception and hypersensitivity.

Authors:  Zhuo-Min Lu; Fang Xie; Han Fu; Ming-Gang Liu; Fa-Le Cao; Jian Hao; Jun Chen
Journal:  Neurochem Res       Date:  2008-04-11       Impact factor: 3.996

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