2003
DOI: 10.1016/s0378-8741(02)00295-7
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Anti-inflammatory and anti-nociceptive effects of Sphaeranthus senegalensis

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Cited by 98 publications
(85 citation statements)
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“…Acetic acid, a commonly used model for assessing the anti-nociceptive effects of drugs, causes an increase in peritoneal fluid of prostaglandin (PG) E2 and PGF2α involving in part, peritoneal pain receptor. 7 The comparable effects of the extract (200 and 400 mg/kg) and aspirin (100 mg/kg) ( Table 1) is a clear indication that the extract may have a similar mechanism of action with aspirin. Aspirin is a weak acid and NSAID, which is effective against mild or moderate pain, especially that arising from inflammation or damaged tissue.…”
Section: Discussionmentioning
confidence: 94%
See 1 more Smart Citation
“…Acetic acid, a commonly used model for assessing the anti-nociceptive effects of drugs, causes an increase in peritoneal fluid of prostaglandin (PG) E2 and PGF2α involving in part, peritoneal pain receptor. 7 The comparable effects of the extract (200 and 400 mg/kg) and aspirin (100 mg/kg) ( Table 1) is a clear indication that the extract may have a similar mechanism of action with aspirin. Aspirin is a weak acid and NSAID, which is effective against mild or moderate pain, especially that arising from inflammation or damaged tissue.…”
Section: Discussionmentioning
confidence: 94%
“…The experiment was carried out by measuring tail withdrawal time from hot water as described by Adzu et al 7 30 mice were randomly divided into five groups (A-E) of six mice each and fasted for 12 hrs. The mice were treated as follows; Group A served as negative control and received 10 ml/kg distilled water per os, Group B served as positive control and received pentazocine (3 mg/kg) intraperitoneally while Group C-E received OTE (50, 100, and 200 mg/kg, respectively) per os.…”
Section: Effects Of Ote On Tail Flick Response In Micementioning
confidence: 99%
“…The response is thought to be mediated by peritoneal mast cells [19], acid sensing ion channels [20] and the prostaglandin pathways [21]. The organic acid has also been postulated to act indirectly by inducing the release of endogenous mediators, which stimulates the nociceptive neurons that are sensitive to NSAIDs and narcotics [22]. It is well known that non-steroidal anti-inflammatory and analgesic drugs mitigate the inflammatory pain by inhibiting the formation of pain mediators at the peripheral target sites where prostaglandins and bradykinin are proposed to play a significant role in the pain process [23].…”
Section: Resultsmentioning
confidence: 99%
“…The tail immersion thermal pain test investigates pain primarily of spinal origin. 23 Pregabalin is a well-established anticonvulsant and analgesic agent that has shown efficacy and dose dependent effects either as monotherapy or in combination with analgesics in relieving pain and related symptoms. It is noteworthy that pregabalin has received Food and Drug Association (FDA) approval for the treatment of diabetic neuropathy and post-herpetic neuralgia.…”
Section: Discussionmentioning
confidence: 99%