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Cassia alata, a traditional herb with a global presence, is renowned for its anti-inflammatory, antibacterial, and antifungal properties, making it a go-to remedy for skin ailments. While it has demonstrated wound healing capabilities in both in vitro and in vivo studies, the precise mechanisms remain elusive. This review aims to highlight its key phytochemicals, their effects, and the mechanism of action. The compounds that have been reviewed and discussed include kaempferol, apigenin, quercetin, rhein, and rutin. These polyphenols play important roles in normal and impaired wound healing processes, encompassing hemostasis, inflammation, proliferation, and tissue remodeling. [ABSTRACT FROM AUTHOR]

Mitragyna speciosa Korth., also known as ketum or kratom, is a tropical plant native to Southeast Asia. Mitragynine is its major active alkaloid. It is traditionally used as treatment for various conditions, including fever. The crude extract of M. speciosa leaves has been proven to have anti-inflammatory and analgesic properties. In general, M. speciosa induces a dose-dependent effect, inducing a stimulant effect at low dose and an opioid-like effect at a high dose. This study was conducted to determine the antipyretic effect of mitragynine and methanolic extract of M. speciosa (MSM) using mice as an in vivo pyretic model. Eighty mice were divided into 8 groups: 6 treatment groups (mitragynine: 5, 10, and 20 mg/kg; MSM: 50, 100, and 200 mg/kg) and 2 control groups (20% Tween 80 in 0.9% NaCl; ketoprofen 1 mg/kg). Eighteen hours after induction of pyrexia by inoculation of yeast, rectal temperature was measured every half an hour for 5 hours. Compared to the negative control group, all groups treated with either mitragynine or MSM had significant reduction of rectal temperature at different points of time. The positive control group treated with ketoprofen had significant (P < 0.001) reduction of pyrexia from 0.5 to 5.0 hours after dosing. At 200 mg/kg, MSM has led to the opioid-like effect of hypothermia, possibly due to its synergistic effect with other compounds such as 7-hydroxymitragynine or mitragynine pseudoindoxyl. This article discusses concerns pertaining to toxicity of mitragynine and MSM, and possible involvement of cyclooxygenase and microsomal prostaglandin E2 synthase pathways. In conclusion, mitragynine and MSM possess dose-dependent antipyretic properties in mice. [ABSTRACT FROM AUTHOR]

Melicope ptelefolia is a medicinal herb commonly used in Malaysia to treat fever, pain, wounds, and itches. The present study was conducted to evaluate the antinociceptive activity of the Melicope ptelefolia ethanolic extract (MPEE) using animal models of nociception. The antinociceptive activity of the extract was assessed using acetic acid-induced abdominal writhing, hot-plate, and formalin-induced paw licking tests. Oral administration of MPEE produced significant dose-dependent antinociceptive effects when tested in mice and rats using acetic acid-induced abdominal constriction test and on the second phase of the formalin-induced paw licking test, respectively. It was also demonstrated that MPEE had no effect on the response latency time to the heat stimulus in the thermal model of the hot-plate test. In addition, the antinociception produced by MPEE was not blocked by naloxone. Furthermore, oral administration of MPEE did not produce any effect in motor performance of the rota-rod test and in acute toxicity study no abnormal behaviors as well as mortality were observed up to a dose level of the extract of 5 g/kg. These results indicated that MPEE at all doses investigated which did not produce any sedative and toxic effects exerted pronounce antinociceptive activity that acts peripherally in experimental animals. [ABSTRACT FROM AUTHOR]