File:Assessment of the effect of plasma fraction treatment on chronic and systemic inflammation.webp

Original file(1,778 × 2,351 pixels, file size: 128 KB, MIME type: image/webp)

Captions

Captions

From the study "Reversal of biological age in multiple rat organs by young porcine plasma fraction"

Summary

edit
Description
English: "Blood levels of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) were measured at regular intervals throughout the 155-day period of the experiment. At the end of the experiment, the levels of Nrf2, a pivotal modulator of inflammation, and oxidative stress were measured in brain, heart, lung, and liver of the rats. Detailed values of IL-6, TNF-alpha, and Nrf2 can be found in Supplementary Table S10, Supplementary Table S11, and Supplementary Table S12. The error bars depict two standard errors"

"Chronic inflammation

Inflammation is an important response that helps protect the body, but excess inflammation especially in terms of duration of this response can have very detrimental effects instead. This occurs when inflammation fails to subside and persists indefinitely, a condition referred to as chronic inflammation, which, for reasons not well-understood, increases with age and is associated with a multitude of conditions and pathologies. The levels of two of the most reliable and common biomarkers of chronic inflammation: interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) are found to be considerably higher in old rats (Fig. 6), and these were very rapidly diminished, within days by E5 treatment, to comparable levels with those of young rats. This was especially stark with IL-6. The reduction of these inflammation markers is consistent with the profile of the nuclear factor erythroid 2-like 2 protein (Nrf2), which plays a major role in resolving inflammation, in part by inhibiting the expression of IL-6 and TNF-α. Nrf2 also induces the expression of antioxidants that neutralizes ROS, which is also a significant feature in inflammation [41]. In summary, plasma fraction reduces oxidative stress and chronic inflammation, which are age-associated pan-tissue stresses, to the levels found in young rats."
Date
Source https://link.springer.com/article/10.1007/s11357-023-00980-6
Author Authors of the study: Steve Horvath, Kavita Singh, Ken Raj, Shraddha I. Khairnar, Akshay Sanghavi, Agnivesh Shrivastava, Joseph A. Zoller, Caesar Z. Li, Claudia B. Herenu, Martina Canatelli-Mallat, Marianne Lehmann, Siniša Habazin, Mislav Novokmet, Frano Vučković, Leah C. Solberg Woods, Angel Garcia Martinez, Tengfei Wang, Priscila Chiavellini, Andrew J. Levine, Hao Chen, Robert T. Brooke, Juozas Gordevicius, Gordan Lauc, Rodolfo G. Goya & Harold L. Katcher

Licensing

edit
w:en:Creative Commons
attribution
This file is licensed under the Creative Commons Attribution 4.0 International license.
You are free:
  • to share – to copy, distribute and transmit the work
  • to remix – to adapt the work
Under the following conditions:
  • attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.

File history

Click on a date/time to view the file as it appeared at that time.

Date/TimeThumbnailDimensionsUserComment
current23:12, 27 December 2023Thumbnail for version as of 23:12, 27 December 20231,778 × 2,351 (128 KB)Prototyperspective (talk | contribs)Uploaded a work by Authors of the study: Steve Horvath, Kavita Singh, Ken Raj, Shraddha I. Khairnar, Akshay Sanghavi, Agnivesh Shrivastava, Joseph A. Zoller, Caesar Z. Li, Claudia B. Herenu, Martina Canatelli-Mallat, Marianne Lehmann, Siniša Habazin, Mislav Novokmet, Frano Vučković, Leah C. Solberg Woods, Angel Garcia Martinez, Tengfei Wang, Priscila Chiavellini, Andrew J. Levine, Hao Chen, Robert T. Brooke, Juozas Gordevicius, Gordan Lauc, Rodolfo G. Goya & Harold L. Katcher from https://lin...

There are no pages that use this file.