Bee venom for the treatment of Parkinson's disease: How far is it possible?

被引:18
作者
Awad, Kamal [1 ,2 ]
Abushouk, Abdelrahman Ibrahim [1 ,3 ,4 ]
AbdelKarim, Ahmed Helal [1 ,2 ]
Mohammed, Maged [1 ,2 ]
Negida, Ahmed [1 ,2 ]
Shalash, Ali S. [5 ]
机构
[1] Med Res Grp Egypt, Cairo, Egypt
[2] Zagazig Univ, Fac Med, Zagazig 44519, Egypt
[3] Ain Shams Univ, Fac Med, Cairo, Egypt
[4] NovaMed Med Res Assoc, Cairo, Egypt
[5] Ain Shams Univ, Neurol Dept, Cairo, Egypt
关键词
Complementary therapies; Dopaminergic neurons; Bee venom; Parkinson's disease; SECRETORY PHOSPHOLIPASE A(2); CENTRAL-NERVOUS-SYSTEM; REGULATORY T-CELLS; OXIDATIVE STRESS; IN-VITRO; MOUSE MODEL; MICROGLIAL ACTIVATION; ACUPUNCTURE THERAPY; NEUROBLASTOMA-CELLS; HONEYBEE VENOM;
D O I
10.1016/j.biopha.2017.04.065
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Parkinson's disease (PD) is the second most common neurodegenerative disease, characterized by progressive loss of dopaminergic neurons in the substantia nigra pars compacta leading to depletion of striatal dopamine and motor symptoms as bradykinesia, resting tremors, rigidity, and postural instability. Current therapeutic strategies for PD are mainly symptomatic and may cause motor complications, such as motor fluctuations and dyskinesia. Therefore, alternative medicine may offer an effective adjuvant treatment for PD. Bee venom therapy (BVT) has long been used as a traditional therapy for several conditions, such as rheumatoid arthritis, asthma, and skin diseases. Experimental and clinical studies showed that BVT could be an effective adjuvant treatment for PD. Several mechanisms were suggested for these findings including the ability of BVT to attenuate neuroinflammation, inhibit apoptosis of dopaminergic neurons, protect against glutamate-induced neurotoxicity, and restore normal dopamine levels in the nigrostriatal pathway. In this article, we reviewed and summarized the literature regarding the potential of BVT for the treatment of PD. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:295 / 302
页数:8
相关论文
共 88 条
  • [1] Agmatine induces glutamate release and cell death in cultured rat cerebellar granule neurons
    Abe, K
    Abe, Y
    Saito, H
    [J]. BRAIN RESEARCH, 2003, 990 (1-2) : 165 - 171
  • [2] Neuroprotective mechanisms of plant extracts against MPTP induced neurotoxicity: Future applications in Parkinson's disease
    Abushouk, Abdelrahman Ibrahim
    Negida, Ahmed
    Ahmed, Hussien
    Abdel-Daim, Mohamed M.
    [J]. BIOMEDICINE & PHARMACOTHERAPY, 2017, 85 : 635 - 645
  • [3] Curing neurophobia in medical schools: evidence-based strategies
    Abushouk, Abdelrahman Ibrahim
    Nguyen Minh Duc
    [J]. MEDICAL EDUCATION ONLINE, 2016, 21
  • [4] Ali M.A., 2012, Int. J. Adv. Res. Technol, V1, P69
  • [5] Aloisi F, 1999, ADV EXP MED BIOL, V468, P123
  • [6] Bee Venom and Its Component Apamin as Neuroprotective Agents in a Parkinson Disease Mouse Model
    Alvarez-Fischer, Daniel
    Noelker, Carmen
    Vulinovic, Franca
    Gruenewald, Anne
    Chevarin, Caroline
    Klein, Christine
    Oertel, Wolfgang H.
    Hirsch, Etienne C.
    Michel, Patrick P.
    Hartmann, Andreas
    [J]. PLOS ONE, 2013, 8 (04):
  • [7] Up-regulation of inducible nitric oxide synthase in the substantia nigra by lipopolysaccharide causes microglial activation and neurodegeneration
    Arimoto, T
    Bing, GY
    [J]. NEUROBIOLOGY OF DISEASE, 2003, 12 (01) : 35 - 45
  • [8] Molecular pathways involved in the neurotoxicity of 6-OHDA, dopamine and MPTP: contribution to the apoptotic theory in Parkinson's disease
    Blum, D
    Torch, S
    Lambeng, N
    Nissou, MF
    Benabid, AL
    Sadoul, R
    Verna, JM
    [J]. PROGRESS IN NEUROBIOLOGY, 2001, 65 (02) : 135 - 172
  • [9] Phospholipase A2 structure/function, mechanism, and signaling
    Burke, John E.
    Dennis, Edward A.
    [J]. JOURNAL OF LIPID RESEARCH, 2009, 50 : S237 - S242
  • [10] The Effects of Bee Venom Acupuncture on the Central Nervous System and Muscle in an Animal hSOD1G93A Mutant
    Cai, MuDan
    Choi, Sun-Mi
    Yang, Eun Jin
    [J]. TOXINS, 2015, 7 (03): : 846 - 858