Exploration its Antioxidant and Immunogenic potential of protein: Calendula officinalis and Dianthus chinensis

Author(s):  
Abhishekh Tripathi ◽  
Shubham Tyagi ◽  
Gurpreet Singh ◽  
Karishma Ghosh ◽  
Amit Gupta

Aim and objective: Pollen is reported in flowers and leaves of various medicinal plants and showed its beneficial effect on human health. The objective of our study is to evaluate the antioxidant effect of flowers (Calendula officinalis and Dianthus chinensis) especially pollen protein and also determining its immunogenic effect against specific protein (typhoid vaccine) antigen in human whole blood samples. Methods: In this study, analytical studies were conducted for estimating the protein content using Lowry test and qualitatively determined through high performance thin layer chromatography (HPLC). In addition, immunological studies were also conducted using pollen protein for evaluating its antioxidant potential (using DPPH (2,2-diphenyl-1-picryl-hydrazyl-hydrate) free radical assay) and determined its immunogenic effect using typhoid vaccine antigen and determining its hemolytic effect in human whole blood samples. Results: This work demonstrated that pollen protein content (determined through lowry test) at higher concentrations exhibited a significant declining in antigen specific T cell proliferation using optimized dose of typhoid vaccine antigen in human whole blood samples. In addition, pollen protein showed antioxidant property as well and does not show any hemolytic effect. Conclusion: The current study showed that pollen protein from Calendula officinalis and Dianthus chinensis possesses antioxidant property and less immunogenic in terms of declining in antigen specific T cell proliferation rate.

2021 ◽  
Vol 2 (1) ◽  
pp. 100311
Author(s):  
Daniella C. Terenzi ◽  
Ehab Bakbak ◽  
Justin Z. Trac ◽  
Mohammad Al-Omran ◽  
Adrian Quan ◽  
...  

1994 ◽  
Vol 42 (3) ◽  
pp. 231-241 ◽  
Author(s):  
C. Shenberg ◽  
S. Spiegel ◽  
S. Chaitchik ◽  
P. Jordan ◽  
M. Kitzis ◽  
...  

2014 ◽  
Vol 436 ◽  
pp. 72-77 ◽  
Author(s):  
Li-Ting Liao ◽  
Chi-Chih Liao ◽  
Chiu-Ching Liu ◽  
Ting-Ya Yang ◽  
Giueng-Chueng Wang

2011 ◽  
Vol 412 (23-24) ◽  
pp. 2150-2156 ◽  
Author(s):  
Ming-Song Hsieh ◽  
Tai-Guang Wu ◽  
Chein-Shyong Su ◽  
Wen-Jing Cheng ◽  
Namik Ozbek ◽  
...  

2015 ◽  
Vol 51 (64) ◽  
pp. 12748-12751 ◽  
Author(s):  
Yuhui Wang ◽  
Kai Jiang ◽  
Jiali Zhu ◽  
Ling Zhang ◽  
Hengwei Lin

A novel FRET model employing fluorescent carbon dots and MnO2nanosheets as donor–acceptor pairs is built for GSH sensing.


2011 ◽  
Vol 3 (10) ◽  
pp. 652-660 ◽  
Author(s):  
Martin Schönfelder ◽  
Hande Hofmann ◽  
Patricia Anielski ◽  
Detlef Thieme ◽  
Renate Oberhoffer ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Paolo Gaibani ◽  
Mara Mariconti ◽  
Gloria Bua ◽  
Sonia Bonora ◽  
Davide Sassera ◽  
...  

Molecular methods are important tools in the diagnosis of bloodstream bacterial infections, in particular in patients treated with antimicrobial therapy, due to their quick turn-around time. Here we describe a new broad-range real-time PCR targeting the 23S rDNA gene and capable to detect as low as 10 plasmid copies per reaction of targeted bacterial 23S rDNA gene. Two commercially available DNA extraction kits were evaluated to assess their efficiency for the extraction of plasma and whole blood samples spiked with different amount of eitherStaphylococcus aureusorEscherichia coli, in order to find the optimal extraction method to be used. Manual QIAmp extraction method with enzyme pre-treatment resulted the most sensitive for detection of bacterial load. Sensitivity of this novel assay ranged between 10 and 103 CFU per PCR reaction forE. coliandS. aureusin human whole blood samples depending on the extraction methods used. Analysis of plasma samples showed a 10- to 100-fold reduction of bacterial 23S rDNA in comparison to the corresponding whole blood specimens, thus indicating that whole blood is the preferential sample type to be used in this real-time PCR protocol. Our results thus show that the 23S rDNA gene represents an optimal target for bacteria quantification in human whole blood.


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