google-site-verification=NjYuzjcWjJ9sY0pu2JmuCKlQLgHuwYq4L4hXzAk4Res A New Potassium Channel on the Endoplasmic Reticulum Membrane in a Rat Brain: Electropharmacology and Molecular Evidence - Basic and Clinical Neuroscience
دوره 16، شماره 6 - ( 8-1404 )                   جلد 16 شماره 6 صفحات 1032-1017 | برگشت به فهرست نسخه ها


XML English Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Nazari M, Eliassi A, Saghiri R, Nikbakht F, Fahanik-babaei J. A New Potassium Channel on the Endoplasmic Reticulum Membrane in a Rat Brain: Electropharmacology and Molecular Evidence. BCN 2025; 16 (6) :1017-1032
URL: http://bcn.iums.ac.ir/article-1-2748-fa.html
A New Potassium Channel on the Endoplasmic Reticulum Membrane in a Rat Brain: Electropharmacology and Molecular Evidence. مجله علوم اعصاب پایه و بالینی. 1404; 16 (6) :1017-1032

URL: http://bcn.iums.ac.ir/article-1-2748-fa.html


چکیده:  
Introduction: Several types of ion channels found in the plasma membrane have also been identified in the membranes of intracellular organelles. These ion channels, including potassium channels, play a crucial role in regulating intracellular ion homeostasis. An ATP-sensitive potassium (KATP) channel with various functional roles has been identified in the endo/sarcoplasmic reticulum membranes of both excitable and non-excitable cells. Our previous studies investigated the electropharmacological and molecular properties of KATP and BKCa+2 channels in the rough endoplasmic reticulum (RER) of rat hepatocytes. 
Methods: In this study, for the first time, we described the electropharmacological and molecular properties of the RER KATP channel in rat brain cells using an incorporated single-channel in a planar lipid bilayer and Western blotting. 
Results: The results of the study revealed the presence of a KATP channel with a conductance of 306 pS, and the open probability was found to be voltage-independent at holding potentials ranging from +40 to -60 in an asymmetric solution (200/50 mM KCl; cis/trans). Additionally, we observed that adding ATP (2.5 mM) to both positive and negative potentials, and 100 μM glibenclamide to the positive voltages inhibited channel activity. The addition of 100 mM 5-HD and 100 nM charybdotoxin to the cis side did not affect the channel behavior. Furthermore, a Western blot analysis provided evidence of the expression of Kir6.2, Kir6.1, sulfonylurea receptor (SUR)1, and/or SUR2B, but not SUR2A, in the RER of rat brain fractions.
Conclusion: In this study, we provide strong evidence for the existence of a KATP channel on the RER membrane of rat brain cells, displaying pharmacological properties distinct from those classically described for the plasma membrane and other intracellular organelles.
نوع مطالعه: Original | موضوع مقاله: Cellular and molecular Neuroscience
دریافت: 1402/4/24 | پذیرش: 1403/1/25 | انتشار: 1404/9/7

ارسال نظر درباره این مقاله : نام کاربری یا پست الکترونیک شما:
CAPTCHA

بازنشر اطلاعات
Creative Commons License این مقاله تحت شرایط Creative Commons Attribution-NonCommercial 4.0 International License قابل بازنشر است.

کلیه حقوق این وب سایت متعلق به Basic and Clinical Neuroscience می باشد.

طراحی و برنامه نویسی : یکتاوب افزار شرق

© 2026 CC BY-NC 4.0 | Basic and Clinical Neuroscience

Designed & Developed by : Yektaweb