Therapeutic Effects of Light Flicker Stimulation in a Mouse Model of Depression - A Comparative Study / (Record no. 615167)

000 -LEADER
fixed length control field 02488nam a22001577a 4500
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 610
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Hyder, Azan
245 ## - TITLE STATEMENT
Title Therapeutic Effects of Light Flicker Stimulation in a Mouse Model of Depression - A Comparative Study /
Statement of responsibility, etc. Azan Hyder
264 ## - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Islamabad :
Name of producer, publisher, distributor, manufacturer SMME- NUST;
Date of production, publication, distribution, manufacture, or copyright notice 2025.
300 ## - PHYSICAL DESCRIPTION
Extent 80p.
Other physical details Soft Copy
Dimensions 30cm
500 ## - GENERAL NOTE
General note Depression is a common neuropsychiatric condition, characterized by behavioral deficiencies,<br/>mood swings, and cognitive impairments. Although fluoxetine is still a commonly prescribed<br/>antidepressant, its drawbacks, including systemic side effects and delayed therapeutic results,<br/>make it necessary to look at alternative treatments. Using a chronic restraint stress mouse model,<br/>this study examines the effectiveness of 40 Hz light flicker therapy as a novel, non-invasive<br/>neuromodulatory treatment for depression by directly contrasting it with fluoxetine treatment.<br/>Behavioral tests such as the Light-Dark Box, Forced Swim, and Sucrose Preference tests showed<br/>that 40 Hz light stimulation dramatically reduced depressive-like behaviors, frequently<br/>outperforming the effects of fluoxetine. Histopathological examinations showed that parvalbuminexpressing interneurons, which are necessary for gamma oscillatory activity and inhibitory<br/>circuitry, had been protected in the prefrontal cortex (PFC) and hippocampal regions. Increased<br/>expression of brain-derived neurotrophic factor (BDNF) and parvalbumin (PV) was further<br/>validated by molecular experiments, suggesting improved interneuron integrity and<br/>neuroplasticity. These results demonstrate that 40 Hz light flicker therapy facilitates the functional<br/>restoration of brain regions damaged in depression, pointing to distinct mechanisms from those of<br/>traditional medication. Subsequent research endeavors ought to concentrate on refining<br/>stimulation parameters, evaluating long-term safety and effectiveness, and clarifying<br/>electrophysiological mechanisms via supplementary imaging and neurophysiological studies.<br/>Promising translational potential is indicated by ongoing clinical investigations. To conclude, 40<br/>Hz light flicker therapy might prove to be a useful supplement or substitute therapy, providing a<br/>customized, side-effect-free choice for managing depression.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element MS Biomedical Sciences (BMS)
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Supervisor : Dr. Aneeqa Noor
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://10.250.8.41:8080/xmlui/handle/123456789/55408">http://10.250.8.41:8080/xmlui/handle/123456789/55408</a>
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Thesis
Holdings
Withdrawn status Permanent Location Current Location Shelving location Date acquired Full call number Barcode Koha item type
  School of Mechanical & Manufacturing Engineering (SMME) School of Mechanical & Manufacturing Engineering (SMME) E-Books 10/14/2025 610 SMME-TH-1185 Thesis
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