Effects of the Cardiotonic Steroid BD-15 on Renal Tissue in Male Wistar Rats Treated with Lipopolysaccharides

  • Author
  • Pedro Henrique Baia Capanema
  • Co-authors
  • Jéssica Alves Faria , Antonio Pereira Ribeiro Arantes , Lara Gomes Silva , Maria Eduarda Botelho , Kézia Cristina Alves , Carolina Alves de Oliveira Gotelip , Ana Luiza Menezes Barbosa , Gustavo Fernando de Frazão Lima , Sílvia Ramos Silva , Luciana Estefani Drumond de Carvalho , Leandro Augusto de Oliveira Barbosa , Vanessa Faria Cortes , Hérica de lima Santos , José Augusto Ferreira Perez Villar , Grazielle Aparecida Silva Maia , Israel José Pereira Garcia
  • Abstract
  •  

    An experimental model for nephritis induction involves treatment with lipopolysaccharide (LPS). The use of the cardiotonic steroid BD-15 at low concentrations (100 ?g/kg, ip) can interact with Na,K-ATPase, mediating intracellular signaling pathways in renal tissue to mitigate damage caused by LPS-induced inflammation. This study aimed to investigate the effects of BD-15 (100 ?g/kg) on renal tissue through biochemical analyses. A total of 20 male Wistar rats were divided into four groups (N = 5): (1) Saline solution, (2) LPS (250 µg/kg, ip), (3) BD-15 (100 ?g/kg, ip), and (4) LPS (250 ?g/kg, ip) + BD-15 (100 ?g/kg, ip). Each animal received the respective treatment and, after 2 hours, was euthanized in accordance with ethical committee requirements. The following parameters were analyzed: Na,K-ATPase activity, lipid peroxidation index (TBARS), catalase activity, protein carbonylation index, and reduced glutathione (GSH) activity. No significant differences were observed in Na,K-ATPase activity and lipid peroxidation; however, intergroup percentage variations were noted in other experiments. Tukey's multiple comparison test revealed a 46% increase in catalase activity in the LPS group (2) compared to the saline solution group (1). For protein carbonylation, the same test detected a 67% increase in the LPS + BD-15 group (4) compared to the BD-15 group (3). Regarding GSH quantification, a reduction was observed in all groups compared to the saline solution group (1): approximately 31% in the LPS group (2), 32% in the BD-15 group (3), and 33% in the LPS + BD-15 group (4). In summary, the results indicate that LPS induced an inflammatory process, while the cardiotonic steroid BD-15 did not cause significant impacts on renal tissue. When BD-15 was administered after LPS induction, it reduced catalase enzyme activity compared to the group treated with LPS alone, indicating potential nephroprotection.

  • Keywords
  • BD-15, LPS, Kidneys, Na, K-ATPase, Reduced Glutathione.
  • Subject Area
  • Na Pump
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Dear Colleagues and Friends,

We are thrilled to extend a warm welcome to the 8th Annual Meeting of the Cardiotonic Steroids and Na Pump, in collaboration with the Brazilian Society of Pharmacology and Experimental Therapeutic Society (SBFTE) and the Brazilian Society for Biochemistry and Molecular Biology (SBBq). The event is scheduled to take place at the Federal University of São João del Rei (UFSJ) from August 20th to 23rd, 2024.

The Na pump meeting stands as one of Brazil's most enduring scientific gatherings. Over the past decade, it has been hosted by various Brazilian institutions, serving as a pivotal platform for scientific discussions that contribute significantly to the advancement of fundamental knowledge in Na, K-ATPase biochemistry, molecular biology, and related fields. Additionally, it serves as a forum for dialogues on scientific education and training, generating consensus that can influence public policies for the betterment of society.

For this year's meeting, the organizing committee has curated an engaging interdisciplinary program, featuring lectures by esteemed foreign scientists. These sessions will delve into the latest advancements and current challenges across a broad spectrum of research topics in Biochemistry and the Molecular Na pump signaling cascade.

We eagerly anticipate your participation in this exciting scientific event and hope to see you soon in Minas Gerais!

Best regards,

Scientific Committee

Comissão Organizadora

Dr Leandro Augusto Barbosa

Dr Vanessa Faria Cortes

Sílvia Ramos Silva 
Marina Vieira

Anna Karolina de Oliveira Alfenas Gadelha - Mídias Sociais e Papelaria
Jessica Alves Faria -  Coffee Break e Gráfica
Lucas Antônio Lisboa Ribeiro - Apresentação/Cerimonial
Poliana Amorim Santos - Abertura/ Encerramento/ parte recreativa
?Ana Gabriela Finamore dos Santo-Midias Sociais e Suporte Técnico.
Thiago Malverde de Oliveira - Divulgação (SJDR) e suporte

Maurício Gustavo Oliveira - Credenciamento
Ítalo Leonardo Diogo - Contato com a pós-graduação e Controle de Frequência
Julia Lopes Granato - Midias sociais e controle de frequência

 

Comissão Científica

Dr. Gustavo Blanco – Kansas University Medical Center, USA

Dr. John Hamlyn – University of Maryland, USA

Dr. Rúben Gerardo Contreras Patiño – CINVESTAV, Mexico

Dra. Vanessa Faria Cortes - Federal University of São João del-Rei, Brazil

Dr Carlos Frederico Leite Fontes - Federal University of Rio de Janeiro, Brazil

Dr Cristoforo Scavone - University of Sao Paulo

 

 

 

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