Analgesic effect of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one in experimental animal models of nociception
Curcuminoids derived from turmeric rhizome have been reported to exhibit antinociceptive, antioxidant and anti-inflammatory activities. We evaluated the peripheral and central antinociceptive activities of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one (DHHPD), a novel syn...
| Main Authors: | , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI
2018
|
| Online Access: | http://psasir.upm.edu.my/id/eprint/15344/ http://psasir.upm.edu.my/id/eprint/15344/1/15344.pdf |
| _version_ | 1848842651002994688 |
|---|---|
| author | Kamarudin, Nur Nadhirah Hisamuddin, Nadia Ong, Hui Ming Ahmad Azmi, Ahmad Farhan Leong, Sze Wei Abas, Faridah Sulaiman, Mohd Roslan Shaik Mohamed Mossadeq, Wan Mastura |
| author_facet | Kamarudin, Nur Nadhirah Hisamuddin, Nadia Ong, Hui Ming Ahmad Azmi, Ahmad Farhan Leong, Sze Wei Abas, Faridah Sulaiman, Mohd Roslan Shaik Mohamed Mossadeq, Wan Mastura |
| author_sort | Kamarudin, Nur Nadhirah |
| building | UPM Institutional Repository |
| collection | Online Access |
| description | Curcuminoids derived from turmeric rhizome have been reported to exhibit antinociceptive, antioxidant and anti-inflammatory activities. We evaluated the peripheral and central antinociceptive activities of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one (DHHPD), a novel synthetic curcuminoid analogue at 0.1, 0.3, 1 and 3 mg/kg (intraperitoneal), through chemical and thermal models of nociception. The effects of DHHPD on the vanilloid and glutamatergic systems were evaluated through the capsaicin- and glutamate-induced paw licking tests. Results showed that DHHPD significantly (p < 0.05) attenuated the writhing response produced by the 0.8% acetic acid injection. In addition, 1 and 3 mg/kg of DHHPD significantly (p < 0.05) reduced the licking time spent by each mouse in both phases of the 2.5% formalin test and increased the response latency of mice on the hot-plate. However, the effect produced in the latter was not reversed by naloxone, a non-selective opioid receptor antagonist. Despite this, DHHPD decreased the licking latency of mice in the capsaicin- and glutamate-induced paw licking tests in a dose response manner. In conclusion, DHHPD showed excellent peripheral and central antinociceptive activities possibly by attenuation of the synthesis and/or release of pro-inflammatory mediators in addition to modulation of the vanilloid and glutamatergic systems without an apparent effect on the opioidergic system. |
| first_indexed | 2025-11-15T08:02:31Z |
| format | Article |
| id | upm-15344 |
| institution | Universiti Putra Malaysia |
| institution_category | Local University |
| language | English |
| last_indexed | 2025-11-15T08:02:31Z |
| publishDate | 2018 |
| publisher | MDPI |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | upm-153442019-07-08T07:29:58Z http://psasir.upm.edu.my/id/eprint/15344/ Analgesic effect of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one in experimental animal models of nociception Kamarudin, Nur Nadhirah Hisamuddin, Nadia Ong, Hui Ming Ahmad Azmi, Ahmad Farhan Leong, Sze Wei Abas, Faridah Sulaiman, Mohd Roslan Shaik Mohamed Mossadeq, Wan Mastura Curcuminoids derived from turmeric rhizome have been reported to exhibit antinociceptive, antioxidant and anti-inflammatory activities. We evaluated the peripheral and central antinociceptive activities of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one (DHHPD), a novel synthetic curcuminoid analogue at 0.1, 0.3, 1 and 3 mg/kg (intraperitoneal), through chemical and thermal models of nociception. The effects of DHHPD on the vanilloid and glutamatergic systems were evaluated through the capsaicin- and glutamate-induced paw licking tests. Results showed that DHHPD significantly (p < 0.05) attenuated the writhing response produced by the 0.8% acetic acid injection. In addition, 1 and 3 mg/kg of DHHPD significantly (p < 0.05) reduced the licking time spent by each mouse in both phases of the 2.5% formalin test and increased the response latency of mice on the hot-plate. However, the effect produced in the latter was not reversed by naloxone, a non-selective opioid receptor antagonist. Despite this, DHHPD decreased the licking latency of mice in the capsaicin- and glutamate-induced paw licking tests in a dose response manner. In conclusion, DHHPD showed excellent peripheral and central antinociceptive activities possibly by attenuation of the synthesis and/or release of pro-inflammatory mediators in addition to modulation of the vanilloid and glutamatergic systems without an apparent effect on the opioidergic system. MDPI 2018 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/15344/1/15344.pdf Kamarudin, Nur Nadhirah and Hisamuddin, Nadia and Ong, Hui Ming and Ahmad Azmi, Ahmad Farhan and Leong, Sze Wei and Abas, Faridah and Sulaiman, Mohd Roslan and Shaik Mohamed Mossadeq, Wan Mastura (2018) Analgesic effect of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one in experimental animal models of nociception. Molecules, 23 (9). art. no. 2099. pp. 1-15. ISSN 1420-3049 https://www.mdpi.com/1420-3049/23/9/2099 10.3390/molecules23092099 |
| spellingShingle | Kamarudin, Nur Nadhirah Hisamuddin, Nadia Ong, Hui Ming Ahmad Azmi, Ahmad Farhan Leong, Sze Wei Abas, Faridah Sulaiman, Mohd Roslan Shaik Mohamed Mossadeq, Wan Mastura Analgesic effect of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one in experimental animal models of nociception |
| title | Analgesic effect of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one in experimental animal models of nociception |
| title_full | Analgesic effect of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one in experimental animal models of nociception |
| title_fullStr | Analgesic effect of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one in experimental animal models of nociception |
| title_full_unstemmed | Analgesic effect of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one in experimental animal models of nociception |
| title_short | Analgesic effect of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one in experimental animal models of nociception |
| title_sort | analgesic effect of 5-(3,4-dihydroxyphenyl)-3-hydroxy-1-(2-hydroxyphenyl)penta-2,4-dien-1-one in experimental animal models of nociception |
| url | http://psasir.upm.edu.my/id/eprint/15344/ http://psasir.upm.edu.my/id/eprint/15344/ http://psasir.upm.edu.my/id/eprint/15344/ http://psasir.upm.edu.my/id/eprint/15344/1/15344.pdf |