Kyotorphin transport and metabolism in rat and mouse neonatal astrocytes.

Author: HuYongjun, JiangHuidi, KeepRichard F, SmithDavid E, XiangJianming

Paper Details 
Original Abstract of the Article :
Neuropeptide inactivation is generally thought to occur via peptidase-mediated degradation. However, a recent study found increased analgesia after L-kyotorphin (L-Tyr-L-Arg; L-KTP) administration in mice lacking an oligopeptide transporter, PEPT2. The current study examines the role of PEPT2 in L-K...See full text at original site
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引用元:
https://pubmed.ncbi.nlm.nih.gov/20537989

データ提供:米国国立医学図書館(NLM)

Kyotorphin: A Journey Through the Desert of the Brain

Greetings, fellow explorers! Dr. Camel here, and I'm always fascinated by the complexities of the brain, a true desert of knowledge. This study investigates kyotorphin, a neuropeptide that plays a role in pain signaling. Imagine a desert caravan, traveling across a vast and unforgiving landscape. Kyotorphin is like a message sent from one oasis to another, carrying information about the journey's challenges.

The researchers explored the transport and metabolism of kyotorphin in astrocytes, star-shaped cells that support neurons in the brain. They found that astrocytes both transport and degrade kyotorphin, like a desert oasis that both attracts and eventually consumes water.

The Desert's Hidden Oasis

The researchers discovered that kyotorphin is transported by a specific transporter protein called PEPT2. It's like a special camel that carries the message from one oasis to another, ensuring it reaches its destination.

Navigating the Desert of Pain

This research sheds light on the complex mechanisms of pain signaling in the brain. It's like unraveling the hidden secrets of the desert, understanding the intricate network of pathways that connect its diverse landscapes.

Dr.Camel's Conclusion

This research provides valuable insights into the transport and metabolism of kyotorphin in astrocytes. It's a reminder that even within the seemingly simple desert, complex processes are constantly at work.

Date :
  1. Date Completed 2010-11-02
  2. Date Revised 2021-10-20
Further Info :

Pubmed ID

20537989

DOI: Digital Object Identifier

NIHMS218129

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Languages

English

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