Sea urchin (Diadema savignyi) extract as a novel protective agent against cisplatin induced neurotoxicity in rats

被引:3
|
作者
Khalil, Eman A. [1 ]
Swelim, Hamdy [2 ]
El-Tantawi, Hala [2 ]
Abdellatif, Ahmed [1 ]
机构
[1] Amer Univ Cairo, Sch Sci & Engn, Dept Biol, Cairo 11835, Egypt
[2] Ain Shams Univ, Fac Sci, Dept Zool, Cairo, Egypt
来源
BMC PHARMACOLOGY & TOXICOLOGY | 2023年 / 24卷 / 01期
关键词
Neurotoxicity; Cisplatin; Cisplatin induced toxicity; GFAP; Bcl2; Sea urchins; Oxidative stress; Diadema Savignyi; ANTICANCER DRUG CISPLATIN; OXIDATIVE STRESS; PERIPHERAL NEUROPATHY; NATURAL-PRODUCTS; ANTIOXIDANT; BRAIN; PAIN; CHEMOTHERAPY; ECHINOCHROME; MODELS;
D O I
10.1186/s40360-023-00651-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Neurotoxicity is a severe side effect of platinum compounds used for cancer chemotherapy such as Cisplatin. This neurotoxicity leads to severe cognitive and nervous dysfunction, therefore, limiting the dose of Cisplatin and compromising the treatment protocol.The present study investigates the neuroprotective effect of Sea Urchins which is a marine animal known for its rich bioactive compounds. Male Sprague Dawley rats received Cisplatin (2 mg/kg body weight) for 4 weeks, two times per week, followed by Sea Urchin extracts (50 and 100 mg/kg body weight) twice weekly for 4 weeks.Results show that rats treated with Urchin's extracts showed a significant improvement in the thermal (heat and cold) sensitivity compared to untreated rats. Liver enzymes Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) and Urea levels were also significantly decreased back to normal following treatment with sea urchin extracts. Brain tissue oxidative stress marker Nitric oxide (NO) and lipid peroxidation marker Malondialdehyde (MDA) increased significantly in the cisplatin-treated rats while the reduced glutathione levels (GSH) and catalase activity (CAT) showed a significant decrease. Treatment with sea Urchin extracts reversed these changes.Histological and immunohistochemical examination of the cerebral cortex reveled degenerative changes such as karyopyknosis and shrunken necrotic ghost like neurons in the cisplatin treated groups. There was also strong positive Glial fibrillary acidic protein (GFAP) reactivity and a negative B-cell leukemia/lymphoma 2 protein (Bcl2) reaction in most apparent neurons, indicating strong apoptotic changes. Treatment with Urchin extracts reversed these changes. Quantification of cerebral cortex neurons also revealed the strong effect of the extracts. Cisplatin treated groups showed 3708 cells/ mm3 compared to 8091 cells/mm(3) in the normal rats. Extract treatment increased the neuronal numbers to almost normal levels. Quantification of the Immuno-histochemical expression of GFAP showed an increase by 10-folds after cisplatin administration. A remarkable decline from the cisplatin group was seen in the extract treated groups.In Conclusion, Sea Urchins extracts possess a strong neuroprotective activity and could provide a novel therapeutic method to prevent Cisplatin-induced neurotoxicity.
引用
收藏
页数:14
相关论文
共 50 条
  • [31] The protective effect of astaxanthin against cisplatin-induced nephrotoxicity in rats
    Akca, Gorkem
    Eren, Huseyin
    Tumkaya, Levent
    Mercantepe, Tolga
    Horsanali, Mustafa Ozan
    Deveci, Ezgi
    Dil, Eyup
    Yilmaz, Adnan
    BIOMEDICINE & PHARMACOTHERAPY, 2018, 100 : 575 - 582
  • [32] Protective effect of aminoguanidine against nephrotoxicity induced by cisplatin in normal rats
    Mansour, MA
    Mostafa, AM
    Nagi, MN
    Khattab, MM
    Al-Shabanah, OA
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2002, 132 (02): : 123 - 128
  • [33] Protective effect of captopril against cisplatin-induced nephrotoxicity in rats
    El-Sayed, El-Sayed M.
    Abd-Ellah, Mohamed F.
    Attia, Sabry M.
    PAKISTAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 21 (03) : 255 - 261
  • [34] Protective effects of methimazole against cisplatin-induced nephrotoxicity in rats
    Braunlich, H
    Appenroth, D
    Fleck, C
    JOURNAL OF APPLIED TOXICOLOGY, 1997, 17 (01) : 41 - 45
  • [35] Protective effects of Polygala paniculata extract against methylmercury-induced neurotoxicity in mice
    Farina, M
    Franco, JL
    Ribas, CM
    Meotti, FC
    Missau, FC
    Pizzolatti, MG
    Dafre, AL
    Santos, ARS
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2005, 57 (11) : 1503 - 1508
  • [36] Protective effects of succimer against lead induced neurotoxicity in developing brain of rats
    Sudhakar, K.
    Deepaktarun, C. H.
    Bhavya, G. B.
    Reddy, K. P.
    JOURNAL OF ENVIRONMENTAL BIOLOGY, 2019, 40 (01): : 89 - 95
  • [37] Potential protective effect of taurine against dibromoacetonitrile-induced neurotoxicity in rats
    Sayed, Rabab H.
    Salem, Hesham A.
    El-Sayeh, Bahia M.
    ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2012, 34 (03) : 849 - 857
  • [38] Histological, ultrastructural and immunohistochemical studies on the protective effect of ginger extract against cisplatin-induced nephrotoxicity in male rats
    Ali, Doaa A.
    Abdeen, Ahmed M.
    Ismail, Mohammed F.
    Mostafa, Mai A.
    TOXICOLOGY AND INDUSTRIAL HEALTH, 2015, 31 (10) : 869 - 880
  • [39] Protective effect of hydroethanolic leaf extract of Parquetina nigrescens against D-galactose-induced neurotoxicity in male Wistar rats
    Ajayi, Lydia Oluwatoyin
    Ayeleso, Ademola Olabode
    Oyedepo, Temitope Adenike
    CHEMICAL BIOLOGY LETTERS, 2021, 8 (02): : 79 - 87
  • [40] Protective role of Panax ginseng extract standardized with ginsenoside Rg3 against acrylamide-induced neurotoxicity in rats
    Mannaa, Fathia
    Abdel-Wahhab, Mosaad A.
    Ahmed, Hanaa H.
    Park, Myung H.
    JOURNAL OF APPLIED TOXICOLOGY, 2006, 26 (03) : 198 - 206