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Non-neurotoxic activity of Malayan krait (Bungarus candidus) venom from Thailand
Charoenpitakchai, Mongkon; Wiwatwarayos, Kulachet; Jaisupa, Nattapon; Rusmili, Muhamad Rusdi Ahmad; Mangmool, Supachoke; Hodgson, Wayne C; Ruangpratheep, Chetana; Chanhome, Lawan; Chaisakul, Janeyuth.
Afiliação
  • Charoenpitakchai, Mongkon; Phramongkutklao College of Medicine. Department of Pathology. Bangkok. TH
  • Wiwatwarayos, Kulachet; Royal Thai Army Medical Department. Army Institute of Pathology. Department of Anatomical Pathology. Bangkok. TH
  • Jaisupa, Nattapon; Phramongkutklao College of Medicine. Department of Pharmacology. Bangkok. TH
  • Rusmili, Muhamad Rusdi Ahmad; International Islamic University Malaysia. Kulliyyah of Pharmacy. Kuantan. MY
  • Mangmool, Supachoke; Mahidol University. Faculty of Pharmacy. Department of Pharmacology. Bangkok. TH
  • Hodgson, Wayne C; Monash University. Biomedical Discovery Institute. Department of Pharmacology. Clayton. AU
  • Ruangpratheep, Chetana; Phramongkutklao College of Medicine. Department of Pathology. Bangkok. TH
  • Chanhome, Lawan; Thai Red Cross Society. Queen Saovabha Memorial Institute. Bangkok. TH
  • Chaisakul, Janeyuth; Phramongkutklao College of Medicine. Department of Pharmacology. Bangkok. TH
J. venom. anim. toxins incl. trop. dis ; 24: 1-9, 2018. tab, graf, ilus
Article em En | LILACS, VETINDEX | ID: biblio-1484743
Biblioteca responsável: BR68.1
Localização: BR68.1
ABSTRACT

Background:

Envenoming by kraits (genus Bungarus) is a medically significant issue in South Asia and Southeast Asia. Malayan krait (Bungarus candidus) venom is known to contain highly potent neurotoxins. In recent years, there have been reports on the non-neurotoxic activities of krait venom that include myotoxicity and nephrotoxicity. However, research on such non-neurotoxicity activities of Malayan krait venom is extremely limited. Thus, the aim of the present study was to determine the myotoxic, cytotoxic and nephrotoxic activities of B. candidus venoms from northeastern (BC-NE) and southern (BC-S) Thailand in experimentally envenomed rats.

Methods:

Rats were administered Malayan krait (BC-NE or BC-S) venom (50 g/kg, i.m.) or 0.9% NaCl solution (50 L, i.m.) into the right hind limb. The animals were sacrificed 3, 6 and 24 h after venom administration. The right gastrocnemius muscle and both kidneys were collected for histopathological analysis. Blood samples were also taken for determination of creatine kinase (CK) and lactate dehydrogenase (LDH) levels. The human embryonic kidney cell line (HEK-293) was used in a cell proliferation assay to determine cytotoxic activity.

Results:

Administration of BC-NE or BC-S venom (50 g/kg, i.m.) caused time-dependent myotoxicity, characterized by an elevation of CK and LDH levels. Histopathological examination of skeletal muscle displayed marked muscle necrosis and myofiber disintegration 24 h following venom administration. Both Malayan krait venoms also induced extensive renal tubular injury with glomerular and interstitial congestion in rats. BC-NE and BC-S venoms (1000.2 g/ mL) caused concentration-dependent cytotoxicity on the HEK-293 cell line. However, BC-NE venom (IC50 =8 ± 1 g/mL; at 24 h incubation; n = 4) was found to be significantly more cytotoxic than BC-S venom (IC50 =15 ± 2 g/mL; at 24 h incubation; n = 4). In addition, the PLA2 activity of BC-NE venom was significantly higher than that of BC-S venom...
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Texto completo: 1 Base de dados: LILACS / VETINDEX Idioma: En Revista: J. venom. anim. toxins incl. trop. dis Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: LILACS / VETINDEX Idioma: En Revista: J. venom. anim. toxins incl. trop. dis Ano de publicação: 2018 Tipo de documento: Article