Abstract

Scorpion venoms are natural sources of molecules that have, in addition to their toxic function, potential therapeutic applications. In this source the neurotoxins can be found especially those that act on potassium channels. Potassium channels are responsible for maintaining the membrane potential in the excitable cells, especially the voltage-dependent potassium channels (Kv), including Kv1.3 channels. These channels (Kv1.3) are expressed by various types of tissues and cells, being part of several physiological processes. However, the major studies of Kv1.3 are performed on T cells due its importance on autoimmune diseases. Scorpion toxins capable of acting on potassium channels (KTx), mainly on Kv1.3 channels, have gained a prominent role for their possible ability to control inflammatory autoimmune diseases. Some of these toxins have already left bench trials and are being evaluated in clinical trials, presenting great therapeutic potential. Thus, scorpion toxins are important natural molecules that should not be overlooked in the treatment of autoimmune and other diseases.

Highlights

  • Venomous animals are specialized predators that developed high degree of complexity compounds for their own biological purposes [1]

  • Knowing that T-effector memory lymphocytes (TEM) cells are responsible for the development of autoimmune diseases, the studies with modulation of voltage-gated potassium channel type 1 (Kv1).3 channels have mightily intensified aiming new therapies using this receptor as target

  • The Kv1.3 channels had already proved their potential as a therapeutic target to treat diseases, such as cancer and autoimmune diseases

Read more

Summary

Introduction

Venomous animals are specialized predators that developed high degree of complexity compounds for their own biological purposes [1]. Knowing that TEM cells are responsible for the development of autoimmune diseases, the studies with modulation of Kv1.3 channels have mightily intensified aiming new therapies using this receptor as target.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call