Journal of ethnopharmacology · 2026
Phytochemical characterization, molecular docking, and protective efficacy of Cleome droserifolia against cisplatin-induced testicular toxicity.
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Alqahtani Moneerah J, El-Sherbeni Suzy A, Negm Walaa A, Elekhnawy Engy, Ibrahim Sarah, Hussein Ismail A, Alanzi Abdullah R, Ahmed Rehab, Balaha Marwa, El-Kadem Aya H
Аннотация
ETHNOPHARMACOLOGICAL RELEVANCE: Cleome droserifolia (CD) has been employed traditionally by the Egyptians inhabiting desert for hyperglycemia treatment.
AIM OF THE STUDY: We aimed to evaluate the capability of CD to lessen the detrimental consequences of cisplatin (CP) on testis.
METHODS: CD phytoconstituents were studied by LC-ESI-MS/MS. The in vivo study involved four groups of forty male rats. Group I had a normal saline intraperitoneal (IP) injection daily; groups II, III, and IV had a single IP injection of 7 mg/kg of CP. Groups III and IV were orally administered 100 and 200 mg/kg of CD, respectively. They were treated daily for 10 days, and a single dose of IP injection of CP was taken on the third day.
RESULTS: The LC-ESI-MS/MS exposed presence of 33 different compounds in CD. Also, CD at 200 mg/kg considerably reestablished the testicular weight loss and serum testosterone in CP-treated rats. Treatment with CD improved the antioxidant capabilities via downregulating malondialdehyde and increasing catalase and glutathione peroxidase activity as well as nuclear factor erythroid 2-related factor 2 immunostaining. It exerted a significant anti-inflammatory action via its decreasing effect on nuclear factor kappa beta immunostaining, and testicular level of tumor necrosis factor-α. Moreover, it exhibited an anti-apoptotic effect by downregulation of p53 and caspase-3, besides enhancing the B-cell lymphoma 2 immunostaining. In addition, molecular docking studies revealed that the major phytochemicals in CD had favorable binding affinities to the key proteins of apoptosis.
CONCLUSION: CD demonstrated promising antioxidant, anti-inflammatory, and anti-apoptotic properties.
AIM OF THE STUDY: We aimed to evaluate the capability of CD to lessen the detrimental consequences of cisplatin (CP) on testis.
METHODS: CD phytoconstituents were studied by LC-ESI-MS/MS. The in vivo study involved four groups of forty male rats. Group I had a normal saline intraperitoneal (IP) injection daily; groups II, III, and IV had a single IP injection of 7 mg/kg of CP. Groups III and IV were orally administered 100 and 200 mg/kg of CD, respectively. They were treated daily for 10 days, and a single dose of IP injection of CP was taken on the third day.
RESULTS: The LC-ESI-MS/MS exposed presence of 33 different compounds in CD. Also, CD at 200 mg/kg considerably reestablished the testicular weight loss and serum testosterone in CP-treated rats. Treatment with CD improved the antioxidant capabilities via downregulating malondialdehyde and increasing catalase and glutathione peroxidase activity as well as nuclear factor erythroid 2-related factor 2 immunostaining. It exerted a significant anti-inflammatory action via its decreasing effect on nuclear factor kappa beta immunostaining, and testicular level of tumor necrosis factor-α. Moreover, it exhibited an anti-apoptotic effect by downregulation of p53 and caspase-3, besides enhancing the B-cell lymphoma 2 immunostaining. In addition, molecular docking studies revealed that the major phytochemicals in CD had favorable binding affinities to the key proteins of apoptosis.
CONCLUSION: CD demonstrated promising antioxidant, anti-inflammatory, and anti-apoptotic properties.