Table 4.
In vivo studies of luteolin's analgesic effects in neuropathic models.
Animal model | Dose and route of administration of luteolin | Effect | Refs |
---|---|---|---|
male Sprague–Dawley rats | intrathecally administered luteolin 1.5 mg - intraperitoneally administered luteolin 50 mg/kg | Attenuated mechanical and cold hyperalgesia | (62) |
diabetic rats - neuropathy induced by intraperitoneal injection of streptozotocin in rats | intraperitoneally 50 mg/kg, 100 mg/kg and 200 mg/kg | improved the impaired nerve functions, activated Nrf2, increased activities of antioxidant enzymes SOD, GST, GPx and CAT, and reduced ROS production, attenuated hyperalgesia and allodynia in a dose dependent manner | (63) |
sciatic nerve ligated mice luteolin | intraperitoneally 5 mg/kg and 10 mg/kg body weight | reduced hyperalgesia in acute and chronic phase of formalin test | (64) |
Lewis's lung cancer induced bone pain in mice | intraperitoneally 10 mg/kg and 50 mg/kg | ameliorated pain in the pain behavior test in a dose-dependent manner, inhibited activation of glial cells in spinal dorsal root and NLRP3 inflammasome | (65) |