Paper Details 
Original Abstract of the Article :
Oxidative stress-induced cellular senescence and inflammation are important biological events in diabetic nephropathy (DN). Our recent studies have found that pyrroloquinoline quinine (PQQ) has protective effects against HG-induced oxidative stress damage and apoptosis in HK-2 cells. Nevertheless, w...See full text at original site
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引用元:
https://doi.org/10.1016/j.intimp.2019.04.040

データ提供:米国国立医学図書館(NLM)

Pyrroloquinoline Quinine: Fighting the Desert's Storms

This study investigates the potential benefits of pyrroloquinoline quinine (PQQ) in protecting against oxidative stress-induced cellular senescence and inflammation in human renal tubular epithelial cells. Imagine a desert landscape ravaged by strong winds and scorching sun, causing damage and erosion. The study explores the potential of PQQ, a compound found in some foods, to protect against similar damage in the cells of the kidneys.

A Shield Against the Storm

The researchers found that PQQ treatment effectively reduced the expression of inflammation markers and senescence markers in the kidney cells. This is like providing a protective shield against the harsh elements of the desert, preventing damage and preserving the cells’ integrity.

The Desert's Resilience

The study also discovered that PQQ’s protective effects were linked to the Keap1/Nrf2 signaling pathway, a critical pathway for cellular defense. This is like uncovering the desert’s own natural mechanisms for resilience, revealing the pathways that allow life to thrive even in harsh conditions.

Dr. Camel's Conclusion

The study offers a promising glimpse into the potential of PQQ as a protective agent against kidney damage. The researchers’ findings suggest that PQQ, like a desert plant that adapts to its environment, can help protect cells against oxidative stress, offering hope for new strategies to combat kidney disease.

Date :
  1. Date Completed 2020-01-07
  2. Date Revised 2020-01-07
Further Info :

Pubmed ID

31035086

DOI: Digital Object Identifier

10.1016/j.intimp.2019.04.040

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English

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