Molecular Crosstalk Between Catecholamine Neurotransmitters and Neurologically Active Ions (
Na
+
$$ {Na}^{+} $$
,
K
+
$$ {K}^{+} $$
and
Cl
−
$$ {Cl}^{-} $$
) and Ion-Induced Chemical Reactivity: A DFT Study
{"title":"Molecular Crosstalk Between Catecholamine Neurotransmitters and Neurologically Active Ions (\n \n \n \n Na\n +\n \n \n $$ {Na}^{+} $$\n , \n \n \n \n K\n +\n \n \n $$ {K}^{+} $$\n and \n \n \n \n Cl\n −\n \n \n $$ {Cl}^{-} $$\n ) and Ion-Induced Chemical Reactivity: A DFT Study","authors":"Kuppusamy Chandru, Tuhin Pradhan","doi":"10.1002/poc.70091","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Theoretical research on the intermolecular interactions (crosstalk) between catecholamine neurotransmitters (CATs) and neurologically active ions (NAIs) such as <span></span><math>\n <semantics>\n <mrow>\n <msup>\n <mi>Na</mi>\n <mo>+</mo>\n </msup>\n </mrow>\n <annotation>$$ {Na}^{+} $$</annotation>\n </semantics></math>, <span></span><math>\n <semantics>\n <mrow>\n <msup>\n <mi>K</mi>\n <mo>+</mo>\n </msup>\n </mrow>\n <annotation>$$ {K}^{+} $$</annotation>\n </semantics></math> and <span></span><math>\n <semantics>\n <mrow>\n <msup>\n <mi>Cl</mi>\n <mo>−</mo>\n </msup>\n </mrow>\n <annotation>$$ {Cl}^{-} $$</annotation>\n </semantics></math> has been performed using the density functional B3LYP method with 6-311++G (d, p)+SDD basis set in aqueous phase. Complexation energy analysis predicts that average interaction energy between CATs and <span></span><math>\n <semantics>\n <mrow>\n <msup>\n <mi>Na</mi>\n <mo>+</mo>\n </msup>\n </mrow>\n <annotation>$$ {Na}^{+} $$</annotation>\n </semantics></math> ion in aqueous phase is ~−22.9 <span></span><math>\n <semantics>\n <mrow>\n <mtext>kcal</mtext>\n <mo>⋅</mo>\n <msup>\n <mi>mol</mi>\n <mrow>\n <mo>−</mo>\n <mn>1</mn>\n </mrow>\n </msup>\n </mrow>\n <annotation>$$ kcal\\cdot {mol}^{-1} $$</annotation>\n </semantics></math>, which is ~3 times higher (i.e., stronger) than the reported experimental interaction energy between dopamine and dopamine transporter (−7.4 <span></span><math>\n <semantics>\n <mrow>\n <mtext>kcal</mtext>\n <mo>⋅</mo>\n <msup>\n <mi>mol</mi>\n <mrow>\n <mo>−</mo>\n <mn>1</mn>\n </mrow>\n </msup>\n </mrow>\n <annotation>$$ kcal\\cdot {mol}^{-1} $$</annotation>\n </semantics></math>). Interaction with anion (<span></span><math>\n <semantics>\n <mrow>\n <msup>\n <mi>Cl</mi>\n <mo>−</mo>\n </msup>\n </mrow>\n <annotation>$$ {Cl}^{-} $$</annotation>\n </semantics></math>) is weaker than cations (<span></span><math>\n <semantics>\n <mrow>\n <msup>\n <mi>Na</mi>\n <mo>+</mo>\n </msup>\n </mrow>\n <annotation>$$ {Na}^{+} $$</annotation>\n </semantics></math>/<span></span><math>\n <semantics>\n <mrow>\n <msup>\n <mi>K</mi>\n <mo>+</mo>\n </msup>\n </mrow>\n <annotation>$$ {K}^{+} $$</annotation>\n </semantics></math>). NBO charge analysis predicted that <span></span><math>\n <semantics>\n <mrow>\n <msup>\n <mi>Na</mi>\n <mo>+</mo>\n </msup>\n </mrow>\n <annotation>$$ {Na}^{+} $$</annotation>\n </semantics></math> and <span></span><math>\n <semantics>\n <mrow>\n <msup>\n <mi>K</mi>\n <mo>+</mo>\n </msup>\n </mrow>\n <annotation>$$ {K}^{+} $$</annotation>\n </semantics></math> interact with donor atoms (N or O) and <span></span><math>\n <semantics>\n <mrow>\n <mi>π</mi>\n <mo>−</mo>\n <mtext>electron</mtext>\n </mrow>\n <annotation>$$ \\pi - electron $$</annotation>\n </semantics></math> cloud of the benzene ring in CATs whereas <span></span><math>\n <semantics>\n <mrow>\n <msup>\n <mi>Cl</mi>\n <mo>−</mo>\n </msup>\n </mrow>\n <annotation>$$ {Cl}^{-} $$</annotation>\n </semantics></math> ion interacts with the acidic hydrogen of –OH/-CH groups by the formation of H-bonds, which is also supported with structural analysis of complexes. Fukui function analysis indicated that chemical reactivity as well as antioxidant activity of CATs is altered because of the interactions with NAIs. All these analyses suggested that molecular crosstalk between CATs and NAIs might perturb the interactions between CATs and receptors during neurotransmission as well as CATs and transporters during reuptake process.</p>\n </div>","PeriodicalId":16829,"journal":{"name":"Journal of Physical Organic Chemistry","volume":"39 8","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Physical Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/poc.70091","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
Theoretical research on the intermolecular interactions (crosstalk) between catecholamine neurotransmitters (CATs) and neurologically active ions (NAIs) such as , and has been performed using the density functional B3LYP method with 6-311++G (d, p)+SDD basis set in aqueous phase. Complexation energy analysis predicts that average interaction energy between CATs and ion in aqueous phase is ~−22.9 , which is ~3 times higher (i.e., stronger) than the reported experimental interaction energy between dopamine and dopamine transporter (−7.4 ). Interaction with anion () is weaker than cations (/). NBO charge analysis predicted that and interact with donor atoms (N or O) and cloud of the benzene ring in CATs whereas ion interacts with the acidic hydrogen of –OH/-CH groups by the formation of H-bonds, which is also supported with structural analysis of complexes. Fukui function analysis indicated that chemical reactivity as well as antioxidant activity of CATs is altered because of the interactions with NAIs. All these analyses suggested that molecular crosstalk between CATs and NAIs might perturb the interactions between CATs and receptors during neurotransmission as well as CATs and transporters during reuptake process.
期刊介绍:
The Journal of Physical Organic Chemistry is the foremost international journal devoted to the relationship between molecular structure and chemical reactivity in organic systems. It publishes Research Articles, Reviews and Mini Reviews based on research striving to understand the principles governing chemical structures in relation to activity and transformation with physical and mathematical rigor, using results derived from experimental and computational methods. Physical Organic Chemistry is a central and fundamental field with multiple applications in fields such as molecular recognition, supramolecular chemistry, catalysis, photochemistry, biological and material sciences, nanotechnology and surface science.