Evidence map›Paper›PMID 35406709›Full record

ArticleCells2022

GABA Receptors Can Depolarize the Neuronal Membrane Potential via Quantum Tunneling of Chloride Ions: A Quantum Mathematical Study.

Sager Nawafleh, Abdallah Barjas Qaswal, Aiman Suleiman, Obada Alali, Fuad Mohammed Zayed, Mohammad Abu Orabi Al-Adwan, Mo'ath Bani Ali

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Direct energy consumption by inhibitory GABAFrontiers in neuroscience · 2026
    Article
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  3. Management strategies for burning mouth syndrome: a comprehensive review.Journal of oral & facial pain and headache · 2026
    Review
  4. Exploring NanoherbalIranian journal of medical sciences · 2025
    Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Sager NawaflehDepartment of Anesthesia and Intensive Care Unit, The Hashemite University, Zarqa 13115, Jordan.
Abdallah Barjas QaswalSchool of Medicine, The University of Jordan, Amman 11942, Jordan.ORCID 0000-0001-5419-4793
Aiman SuleimanDepartment of Anesthesia, Intensive Care and Pain Management, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.ORCID 0000-0003-2625-4028
Obada AlaliDepartment of Anesthesia and Intensive Care, Alabdali Clemenceau Hospital, Amman 11190, Jordan.
Fuad Mohammed ZayedSchool of Medicine, The University of Jordan, Amman 11942, Jordan.ORCID 0000-0003-3420-029X
Mohammad Abu Orabi Al-AdwanSchool of Medicine, The University of Jordan, Amman 11942, Jordan.
Mo'ath Bani AliSchool of Medicine, The University of Jordan, Amman 11942, Jordan.
University of Jordan · JOBeth Israel Deaconess Medical Center · USHashemite University · JOJordan Hospital · JO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GABA (gamma-aminobutyric acid) receptors represent the major inhibitory receptors in the nervous system and their inhibitory effects are mediated by the influx of chloride ions that tends to hyperpolarize the resting membrane potential. However, GABA receptors can depolarize the resting membrane potential and thus can also show excitatory effects in neurons. The major mechanism behind this depolarization is mainly attributed to the accumulation of chloride ions in the intracellular compartment. This accumulation leads to increase in the intracellular chloride concentration and depolarize the Nernst potential of chloride ions. When the membrane potential is relatively hyperpolarized, this will result in a chloride efflux instead of influx trying to reach their depolarized equilibrium potential. Here, we propose different mechanism based on a major consequence of quantum mechanics, which is quantum tunneling. The quantum tunneling model of ions is applied on GABA receptors and their corresponding chloride ions to show how chloride ions can depolarize the resting membrane potential. The quantum model states that intracellular chloride ions have higher quantum tunneling probability than extracellular chloride ions. This is attributed to the discrepancy in the kinetic energy between them. At physiological parameters, the quantum tunneling is negligible to the degree that chloride ions cannot depolarize the membrane potential. Under certain conditions such as early neuronal development, gain-of-function mutations, stroke and trauma that can lower the energy barrier of the closed gate of GABA receptors, the quantum tunneling is enhanced so that the chloride ions can depolarize the resting membrane potential. The major unique feature of the quantum tunneling mechanism is that the net efflux of chloride ions is attained without the need for intracellular accumulation of chloride ions as long as the energy barrier of the gate is reduced but still higher than the kinetic energy of the chloride ion as a condition for quantum tunneling to take place.

Indexed as

ChloridesReceptors, GABAgamma-Aminobutyric AcidMembrane PotentialsNeuronsChloridesgamma-Aminobutyric AcidReceptors, GABAchloride ionsdepolarizationGABA receptorshyperpolarizationmembrane potentialquantum biologyquantum conductancequantum medicinequantum tunneling

Identifiers

PMID35406709
PMCPMC8998136
OpenAlexW4220698023

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.