Evidence suggesting emotional stress in infancy has significant and far-reaching effects on the body, and could result in disease later in life, has been found.
Psychological stress in infancy dramatically changes the amount of an important class of proteins, called GABAA receptors, which in turn may alter the workings of the heart, lungs, kidneys and bladder. It was already known that changes in the amounts of GABAA receptors causes some brain disorders, but researchers at the University of Portsmouth are the first to show that stress can also alter their expression in other organs.
The research team, from the School of Pharmacy and Biomedical Sciences, studied the way GABAA receptors behave in secondary organs in mice which had first been exposed to stress.
Researcher Dr. Jerome Swinny said:
“GABAA receptors were known to control brain activity and served as important targets for many drugs used in modern medicine to treat brain disorders, such as epilepsy, anxiety as well as inducing surgical anaesthesia. We were surprised to find these proteins were also found to be expressed so widely beyond the brain. The dramatic stress-induced changes in the amounts of GABAA receptor compared to what one normally finds is intriguing. It will alter organ function and, we suggest, will contribute to diseases of the organs.”
The research was carried out in the laboratory of Dr. Swinny, a reader in neuropharmacology and one of the authors.
“It has long been known that childhood adversity, such as neglect or abuse, confers a vulnerability to developing a range of medical conditions later in life, including mental illnesses such as anxiety, and cardiovascular or metabolic disorders. However, precisely how such emotional challenges impact on the normal functioning of different organs within our body remains elusive, which stops the development of effective drug therapies,”
The GABAA receptor (GABAAR) is an ionotropic receptor and ligand-gated ion channel. Its endogenous ligand is γ-aminobutyric acid (GABA), the major inhibitory neurotransmitter in the central nervous system. Upon activation, the GABAA receptor selectively conducts Cl− through its pore.
GABAA receptors are responsible for most of the physiological activities of GABA in the central nervous system, and the receptor subtypes vary significantly. Subunit composition can vary widely between regions and subtypes may be associated with specific functions.
GABAA receptors can also be found in other tissues, including leydig cells, placenta, immune cells, liver, bone growth plates and several other endocrine tissues. Subunit expression varies between “normal” tissue and malignancies, as GABAA receptors can influence cell proliferation.
The human central nervous system is designed to withstand stress, he said, and a certain amount of stress allows humans to adapt and survive in an ever changing environment.
The problems begin when exposure to stress is constant.
“A sustained threat is detrimental to our survival. The nervous system of an infant is not mature enough to be able to cope with prolonged exposure to the chemicals which mediate our stress response. As a result, such experiences often confer a vulnerability to changes to the normal development of their body and mind.
We know a lot about these proteins in the brain and that’s enabled us to develop drugs for associated conditions such as anxiety. We hope that this new understanding of stress and these receptors can eventually be applied to other parts of the body, to treat a wide range of disorders from hypertension, to diabetes, to an upset tummy,”
explained Dr. Swinny.
In summary, the study provides an outline of the diversity of GABAAR subunits, expressed at the mRNA level, in major peripheral organs.
Ethan A. Everington, Adina G. Gibbard, Jerome D. Swinny and Mohsen Seifi
Molecular Characterization of GABA-A Receptor Subunit Diversity within Major Peripheral Organs and Their Plasticity in Response to Early Life Psychosocial Stress
Front. Mol. Neurosci., 06 February 2018 | https://doi.org/10.3389/fnmol.2018.00018
Top Image: GABA-A receptor