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      Honey Bee Venom (Apis mellifera) Contains Anticoagulation Factors and Increases the Blood-clotting Time

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          Abstract

          Objectives:

          Bee venom (BV) is a complex mixture of proteins and contains proteins such as phospholipase and melittin, which have an effect on blood clotting and blood clots. The mechanism of action of honey bee venom (HBV, Apis mellifera) on human plasma proteins and its anti-thrombotic effect were studied. The purpose of this study was to investigate the anti-coagulation effect of BV and its effects on blood coagulation and purification.

          Methods:

          Crude venom obtained from Apis mellifera was selected. The anti-coagulation factor of the crude venom from this species was purified by using gel filtration chromatography (sephadex G-50), and the molecular weights of the anti-coagulants in this venom estimated by using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Blood samples were obtained from 10 rabbits, and the prothrombin time (PT) and the partial thromboplastin time (PTT) tests were conducted. The approximate lethal dose (LD) values of BV were determined.

          Results:

          Crude BV increased the blood clotting time. For BV concentrations from 1 to 4 mg/mL, clotting was not observed even at more than 300 seconds, standard deviations (SDs) = ± 0.71; however, clotting was observed in the control group 13.8 s, SDs = ± 0.52. Thus, BV can be considered as containing anti-coagulation factors. Crude BV is composed 4 protein bands with molecular weights of 3, 15, 20 and 41 kilodalton (kDa), respectively. The LD 50 of the crude BV was found to be 177.8 μg/mouse.

          Conclusion:

          BV contains anti-coagulation factors. The fraction extracted from the Iranian bees contains proteins that are similar to anti-coagulation proteins, such as phospholipase A 2 (PLA 2) and melittin, and that can increase the blood clotting times in vitro.

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          Most cited references24

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          Three Valuable Peptides from Bee and Wasp Venoms for Therapeutic and Biotechnological Use: Melittin, Apamin and Mastoparan

          While knowledge of the composition and mode of action of bee and wasp venoms dates back 50 years, the therapeutic value of these toxins remains relatively unexploded. The properties of these venoms are now being studied with the aim to design and develop new therapeutic drugs. Far from evaluating the extensive number of monographs, journals and books related to bee and wasp venoms and the therapeutic effect of these toxins in numerous diseases, the following review focuses on the three most characterized peptides, namely melittin, apamin, and mastoparan. Here, we update information related to these compounds from the perspective of applied science and discuss their potential therapeutic and biotechnological applications in biomedicine.
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            Bee and wasp venoms.

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              Bee venom reduces neuroinflammation in the MPTP-induced model of Parkinson's disease.

              This study was designed to investigate the anti-inflammatory effects of bee venom (BV) in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced mouse model of Parkinson's disease (PD). MPTP was administered by intraperitoneal (IP) injection at 2-hr intervals over an 8-hr period. Mice were then subjected to BV subcutaneous injection and sacrificed on days 1 and 3 following the final MPTP injection. The loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc) was assessed by tyrosine hydroxylase (TH) immunohistochemistry. Microglial activation was measured by immunohistochemistry for macrophage antigen complex-1 (MAC-1) and inducible nitric oxide synthase (iNOS). The staining intensities of MAC-1 and iNOS were quantified with respect to optical density. In animals treated with MPTP, the survival percentages of TH+ cells in the SNpc were 32% on day 1 and 46% on day 3 compared with normal mice. In BV-treated mice, the survival percentages of TH+ cells improved to 70% on day 1 and 78% on day 3 compared with normal mice. BV treatment also resulted in reduced expression of the inflammation markers MAC-1 and iNOS in the SNpc. These data suggest that BV injection may have a neuroprotective effect that attenuates the activation of the microglial response, which has implications for the treatment of PD.
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                Author and article information

                Contributors
                zolfagharianh@yahoo.com
                mmrpentium@yahoo.com
                m.babaie47@yahoo.com
                Journal
                J Pharmacopuncture
                J Pharmacopuncture
                J Pharmacopunct
                10.3831
                Journal of Pharmacopuncture
                KOREAN PHARMACOPUNCTURE INSTITUTE
                2093-6966
                2234-6856
                December 2015
                : 18
                : 4
                : 7-11
                Affiliations
                [1 ]Department of Venomous Animals and Antivenom Production, Razi Vaccine and Serum Research Institute, Karaj, Iran
                [2 ]Department of Toxicology, School of Pharmacy, Shahreza Branch, Islamic Azad University, Shahreza, Iran
                [3 ]Young Researchers and Elites Club, Science and Research Branch, Islamic Azad University, Tehran, Iran
                Author notes
                * Corresponding Author Hossein Zolfagharian. Department of Venomous Animals and Antivenom Production, Razi Vaccine and Serum Research Institute, Karaj, Iran. Tel: +98-26-3457-0038 Fax: +98-91-2345-1699 Email: zolfagharianh@yahoo.com
                Article
                10.3831/KPI.2015.18.031
                4797586
                26998384
                ae8111b0-4e02-4f05-944f-aa2ee798f50e
                Copyright ©2015, KOREAN PHARMACOPUNCTURE INSTITUTE

                This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 September 2015
                : 29 October 2015
                Categories
                Original Article

                anti-coagulants, bee venom, chromatography, ld50
                anti-coagulants, bee venom, chromatography, ld50

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