Startseite Effect of luteolin on the gene level expression of apoptosis-associated speck-like protein containing a caspase recruitment domain of NLRP3 inflammasome and NF-κB in rats subjected to experimental pancreatitis – influence of HSP70
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Effect of luteolin on the gene level expression of apoptosis-associated speck-like protein containing a caspase recruitment domain of NLRP3 inflammasome and NF-κB in rats subjected to experimental pancreatitis – influence of HSP70

  • Sadanandan Rajapriya und Arumugam Geetha EMAIL logo
Veröffentlicht/Copyright: 24. Juni 2021

Abstract

Objectives

Nod-like receptor pyrin domain containing 3 (NLRP3) is one of the well characterized inflammasome that controls the maturation of pro-inflammatory cytokines and thereby the inflammation in pancreas which could be a promising target for anti-inflammatory drugs. The present study is aimed to explore whether luteolin can target the NLRP3 inflammasome and modulate its activity through the signaling protein, HSP70 in the ethanol-cerulein model of experimental pancreatitis.

Methods

Male albino Wistar rats were divided into four groups. Groups 1 and 2 rats received normal diet. Groups 3 and 4 rats received isocalorically adjusted diet containing ethanol for 5 weeks and cerulein (20 μg/kg body weight i.p., thrice weekly for the last 3 weeks of the experimental period). Additionally, group 2 and 4 rats received 2 mg/kg body weight of luteolin orally from third week.

Results

Luteolin co-administration decreased the serum levels of HSP70, oxidative stress markers, myeloperoxidase, GSH/GSSG and GST with concomitant downregulation in the mRNA expression of HSP70, caspase-1, ASC-NLRP3 and NF-κB. Spearman’s rank correlation test showed that serum HSP70 has positive correlation with the expression of ASC-NLRP3, caspase-1, NF-κB and 4-hydroxynonenal and negative correlation with GSH:GSSG ratio.

Conclusions

The modulating effect of luteolin on the expression of HSP70, NF-κB and thereby on ASC-NLRP3 complex may be claimed for its pancreato-protective activity.


Corresponding author: Arumugam Geetha, Dr. Ambedkar Government Arts College, Chennai 600 039, Tamil Nadu, India, Phone: +91 7904316378, E-mail:

Funding source: Indian Council of Medical Research 10.13039/501100001411

Award Identifier / Grant number: 45/07/2018-BIO/BMS

Acknowledgments

The authors thank Dr. Pramod K. Srivastava, Professor of Immunology and Medicine and Director, Carole and Ray Neag Comprehensive Cancer Center, UConn School of Medicine, Farmington, Connecticut, USA for his generous gift of ELISA kit.

  1. Research funding: Financial support was provided by Indian Council of Medical Research (ICMR) [Senior Research Fellow, File no.: 45/07/2018-BIO/BMS], New Delhi, India.

  2. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  3. Competing interests: The funding organization(s) played no role in the study design, in the collection, analysis and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

  4. Ethical approval: This study was approved by the Committee for the purpose of Control and Supervision of Experiments on Animals (CPCSEA), Government of India, New Delhi, (XVII/VELS/PCOL/14/2000/CPCSEA/IAEC/06.10.15).

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Received: 2020-08-11
Accepted: 2021-04-14
Published Online: 2021-06-24

© 2021 Walter de Gruyter GmbH, Berlin/Boston

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