Antinociception induced by artemisinin nanocapsule in a model of postoperative pain via spinal TLR4 inhibition

Artemisinin (ART) was initially described for the control of inflammation and pain. However, the mechanisms involved with its antinociceptive effect are still poorly understood. Thus, this present study aimed to investigate the effect of ART in both free and nanocapsulated form on postoperative pain...

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Veröffentlicht in:Inflammopharmacology 2020-12, Vol.28 (6), p.1537-1551
Hauptverfasser: Elisei, L. M. S., Moraes, T. R., Malta, I. H., Charlie-Silva, I., Sousa, I. M. O., Veras, F. P., Foglio, M. A., Fraceto, L. F., Galdino, G.
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container_issue 6
container_start_page 1537
container_title Inflammopharmacology
container_volume 28
creator Elisei, L. M. S.
Moraes, T. R.
Malta, I. H.
Charlie-Silva, I.
Sousa, I. M. O.
Veras, F. P.
Foglio, M. A.
Fraceto, L. F.
Galdino, G.
description Artemisinin (ART) was initially described for the control of inflammation and pain. However, the mechanisms involved with its antinociceptive effect are still poorly understood. Thus, this present study aimed to investigate the effect of ART in both free and nanocapsulated form on postoperative pain, as well as the participation of the spinal Toll-like receptor 4 (TLR4) in this process. Postoperative pain was induced using the skin/muscle incision retraction (SMIR) model in male Swiss mice. After 3 and 28 days of SMIR, the animals received an intrathecal injection of free or nanocapsulated ART, and the nociceptive threshold was evaluated by von Frey filament test. To evaluate the involvement of the microglia, astrocytes, and TLR4, minocycline (a microglia inhibitor), fluorocitrate (an astrocyte inhibitor), and Lipopolysaccharide Rhodobacter sphaeroides (LPS-RS), a TLR4 antagonist, were intrathecally injected on the third day of SMIR. The levels of spinal TLR4 protein and proinflammatory cytokines tumor necrosis factor-alpha (TNF-α), and interleukin-1-beta (IL-1β) were quantified by western blot and enzyme-linked immunosorbent assay, respectively. The results showed that free ART reduced postoperative pain ( P  
doi_str_mv 10.1007/s10787-020-00756-w
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M. S. ; Moraes, T. R. ; Malta, I. H. ; Charlie-Silva, I. ; Sousa, I. M. O. ; Veras, F. P. ; Foglio, M. A. ; Fraceto, L. F. ; Galdino, G.</creator><creatorcontrib>Elisei, L. M. S. ; Moraes, T. R. ; Malta, I. H. ; Charlie-Silva, I. ; Sousa, I. M. O. ; Veras, F. P. ; Foglio, M. A. ; Fraceto, L. F. ; Galdino, G.</creatorcontrib><description>Artemisinin (ART) was initially described for the control of inflammation and pain. However, the mechanisms involved with its antinociceptive effect are still poorly understood. Thus, this present study aimed to investigate the effect of ART in both free and nanocapsulated form on postoperative pain, as well as the participation of the spinal Toll-like receptor 4 (TLR4) in this process. Postoperative pain was induced using the skin/muscle incision retraction (SMIR) model in male Swiss mice. After 3 and 28 days of SMIR, the animals received an intrathecal injection of free or nanocapsulated ART, and the nociceptive threshold was evaluated by von Frey filament test. To evaluate the involvement of the microglia, astrocytes, and TLR4, minocycline (a microglia inhibitor), fluorocitrate (an astrocyte inhibitor), and Lipopolysaccharide Rhodobacter sphaeroides (LPS-RS), a TLR4 antagonist, were intrathecally injected on the third day of SMIR. The levels of spinal TLR4 protein and proinflammatory cytokines tumor necrosis factor-alpha (TNF-α), and interleukin-1-beta (IL-1β) were quantified by western blot and enzyme-linked immunosorbent assay, respectively. The results showed that free ART reduced postoperative pain ( P  &lt; 0.001, F 5,30  = 7.49, 16.66% for 1000 ng dose; and P  &lt; 0.01, F 5,30  = 7.49, 14.58% for 500 ng dose) on the 3rd day of SMIR; while the ART nanocapsule had this effect on both the third ( P  &lt; 0.001; F 5,30  = 4.94; 43.75, 39.58 and 72.91% for the 250, 500 and 1000 ng doses, respectively) and 28th ( P  &lt; 0.05; F 5,30  = 7.71; 29.16 and 33.33% for the 500 and 1000 ng doses, respectively) day. The ART nanocapsule had a more potent and longer antinociceptive effect than free ART or morphine. Postoperative pain was also reduced by minocycline and LPS-RS. The ART nanocapsule also reduced the increased levels of TLR4, TNF-α, and IL-1β induced by SMIR. 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Postoperative pain was induced using the skin/muscle incision retraction (SMIR) model in male Swiss mice. After 3 and 28 days of SMIR, the animals received an intrathecal injection of free or nanocapsulated ART, and the nociceptive threshold was evaluated by von Frey filament test. To evaluate the involvement of the microglia, astrocytes, and TLR4, minocycline (a microglia inhibitor), fluorocitrate (an astrocyte inhibitor), and Lipopolysaccharide Rhodobacter sphaeroides (LPS-RS), a TLR4 antagonist, were intrathecally injected on the third day of SMIR. The levels of spinal TLR4 protein and proinflammatory cytokines tumor necrosis factor-alpha (TNF-α), and interleukin-1-beta (IL-1β) were quantified by western blot and enzyme-linked immunosorbent assay, respectively. 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F.</au><au>Galdino, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antinociception induced by artemisinin nanocapsule in a model of postoperative pain via spinal TLR4 inhibition</atitle><jtitle>Inflammopharmacology</jtitle><stitle>Inflammopharmacol</stitle><date>2020-12-01</date><risdate>2020</risdate><volume>28</volume><issue>6</issue><spage>1537</spage><epage>1551</epage><pages>1537-1551</pages><issn>0925-4692</issn><eissn>1568-5608</eissn><abstract>Artemisinin (ART) was initially described for the control of inflammation and pain. However, the mechanisms involved with its antinociceptive effect are still poorly understood. Thus, this present study aimed to investigate the effect of ART in both free and nanocapsulated form on postoperative pain, as well as the participation of the spinal Toll-like receptor 4 (TLR4) in this process. Postoperative pain was induced using the skin/muscle incision retraction (SMIR) model in male Swiss mice. After 3 and 28 days of SMIR, the animals received an intrathecal injection of free or nanocapsulated ART, and the nociceptive threshold was evaluated by von Frey filament test. To evaluate the involvement of the microglia, astrocytes, and TLR4, minocycline (a microglia inhibitor), fluorocitrate (an astrocyte inhibitor), and Lipopolysaccharide Rhodobacter sphaeroides (LPS-RS), a TLR4 antagonist, were intrathecally injected on the third day of SMIR. The levels of spinal TLR4 protein and proinflammatory cytokines tumor necrosis factor-alpha (TNF-α), and interleukin-1-beta (IL-1β) were quantified by western blot and enzyme-linked immunosorbent assay, respectively. The results showed that free ART reduced postoperative pain ( P  &lt; 0.001, F 5,30  = 7.49, 16.66% for 1000 ng dose; and P  &lt; 0.01, F 5,30  = 7.49, 14.58% for 500 ng dose) on the 3rd day of SMIR; while the ART nanocapsule had this effect on both the third ( P  &lt; 0.001; F 5,30  = 4.94; 43.75, 39.58 and 72.91% for the 250, 500 and 1000 ng doses, respectively) and 28th ( P  &lt; 0.05; F 5,30  = 7.71; 29.16 and 33.33% for the 500 and 1000 ng doses, respectively) day. The ART nanocapsule had a more potent and longer antinociceptive effect than free ART or morphine. Postoperative pain was also reduced by minocycline and LPS-RS. The ART nanocapsule also reduced the increased levels of TLR4, TNF-α, and IL-1β induced by SMIR. 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subjects Allergology
Biomedical and Life Sciences
Biomedicine
Dermatology
Gastroenterology
Immunology
Original Article
Pharmacology/Toxicology
Rheumatology
title Antinociception induced by artemisinin nanocapsule in a model of postoperative pain via spinal TLR4 inhibition
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