Effects of mebendazole, albendazole, and praziquantel on fumarate hydratase, pyruvate kinase, and phosphoenolpyruvate carboxykinase of Echinococcus granulosus cyst wall harbored in mice.

Author: FengJ J, GuoH F, JiaoP Y, JiaoW, XiaoS H, YaoM Y

Paper Details 
Original Abstract of the Article :
Echinococcus granulosus cyst wall exhibited activities of fumarate hydratase (FH), pyruvate kinase (PK), and phosphoenolpyruvate carboxykinase (PEPCK) with 911-1433, 151-215, and 54-98U, respectively. The ratio of PK/PEPCK was 2.2-2.7, indicating that glycolysis is the main pathway of carbohydrate m...See full text at original site
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引用元:
https://pubmed.ncbi.nlm.nih.gov/8010090

データ提供:米国国立医学図書館(NLM)

The Impact of Anti-Hydatid Drugs on Echinococcus granulosus Cyst Wall Metabolism

Parasitic infections can be a significant health concern, and the study of their metabolic pathways is crucial for developing effective treatments. This research focuses on Echinococcus granulosus, a parasite that causes hydatid disease. The researchers investigated the effects of three anti-hydatid drugs (mebendazole, albendazole, and praziquantel) on the metabolic activity of the Echinococcus granulosus cyst wall. Their findings provide valuable insights into the mechanism of action of these drugs and the metabolic pathways targeted by them.

Targeting Metabolic Pathways for Effective Treatment

The researchers discovered that mebendazole and albendazole significantly inhibited the activity of pyruvate kinase (PK) and phosphoenolpyruvate carboxykinase (PEPCK) in the cyst wall. These enzymes are crucial for carbohydrate metabolism in the parasite. The findings suggest that these drugs exert their anti-parasitic effects by targeting these specific metabolic pathways. This knowledge is crucial for optimizing treatment strategies and understanding the mechanisms of action of these drugs. It's like navigating a desert where the survival of a caravan depends on understanding the intricate workings of the sand dunes. By understanding the parasite's metabolic pathways, we can effectively target them with medications to disrupt their growth and survival.

Potential for New Treatments

The study's findings provide valuable insights into the metabolic pathways of Echinococcus granulosus, paving the way for the development of new and improved anti-hydatid drugs. By targeting specific metabolic pathways, researchers can design drugs that are more effective and have fewer side effects. It's a reminder that understanding the intricate workings of parasites can lead to significant breakthroughs in treating these infections. Just as a camel caravan relies on its knowledge of the desert to navigate safely, we must continue to unravel the mysteries of parasitic infections to find effective treatments.

Dr.Camel's Conclusion

This research provides a glimpse into the intricate world of parasitic metabolism. By targeting specific metabolic pathways, we can create effective treatments for hydatid disease, offering hope for a future where these infections are no longer a threat.

Date :
  1. Date Completed 1994-07-19
  2. Date Revised 2013-11-21
Further Info :

Pubmed ID

8010090

DOI: Digital Object Identifier

8010090

Related Literature

SNS
PICO Info
in preparation
Languages

English

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