In-Vivo Evaluation Of Silymarin Encapsulated Liposomal Nanoparticles In Chronic Mild Stress (Cms) Model And Depression Induced Liver Disorders / (Record no. 608369)

000 -LEADER
fixed length control field 03187nam a22001577a 4500
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 610
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Fatima, Misha
245 ## - TITLE STATEMENT
Title In-Vivo Evaluation Of Silymarin Encapsulated Liposomal Nanoparticles In Chronic Mild Stress (Cms) Model And Depression Induced Liver Disorders /
Statement of responsibility, etc. Misha Fatima
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 2022.
300 ## - PHYSICAL DESCRIPTION
Extent 77p.
Other physical details Islamabad : SMME- NUST; Soft Copy
Dimensions 30cm
500 ## - GENERAL NOTE
General note Depression is categorized as one of the most prevalent psychological disorders that affect personal<br/>wellbeing and social life of individuals. Symptoms vary from anhedonia to suicide commitment.<br/>The molecular mechanism behind is the low concentration of neurotransmitters serotonin,<br/>dopamine and norepinephrine in central nervous system. These are primarily responsible for<br/>regulating and alleviating mood. In the chronic mild stress (CMS) model of depression, silymarin,<br/>a plant-derived polyphenolic flavonoid of Silybum marianum, elicited strong antidepressant-like<br/>action. It increased the levels of monoamines, particularly 5-hydroxytryptamine (5-HT) in the<br/>cortex and dopamine (DA) in the mice hippocampal region and prefrontal cortex. The objective of<br/>the current research was to investigate silymarin's antidepressant potential in CMS-induced<br/>depressive-like behavior in mice and to identify its potential mechanism(s) of action. The mice<br/>were given silymarin and silymarin loaded liposomal nanoparticles (SLNPs) for two weeks after<br/>following CMS protocol for 28 days (4 weeks). Animals were assessed for behavioral alterations,<br/>including exploratory activity in an open field test, behavioral despair in a forced swim test, and<br/>anxiety-like behaviors in an elevated plus maze test. There lies a close relationship between<br/>depression and inflammatory liver diseases. Hence the effect of depression on liver has also been<br/>checked. Silymarin is a commercially available hepatoprotective drug but due to its antioxidant<br/>properties, research has been conducted to evaluate its neuroprotective effect and hence its<br/>prescription as antidepressant drug. However, due to its poor solubility and bioavailability there is<br/>delay in the onset of treatment outcomes in many individuals. Certain side effects and<br/>contraindications are also important regimen opponents. In this study, Silymarin loaded liposomal<br/>nanoparticles (SLNPs) are prepared, characterized, and realized for the depression treatment in<br/>Chronic Mild Stress (CMS) mice model of depression and its treatment efficiency on symptoms<br/>of inflammatory liver diseases in mice as well. It presented face construct and validity response.<br/>As such the SLNPs present improvement in depression measurement parameters as compared to<br/>the simple silymarin. The SLNPs also positively impacted the aggression, anhedonia and rearing<br/>in mice, however simple silymarin treated mice did not show improvement in social and personal<br/>behavior. As such SLNPs compensated for delayed onset of fluoxetine response.
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. Nosheen Fatima Rana
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://10.250.8.41:8080/xmlui/handle/123456789/31458">http://10.250.8.41:8080/xmlui/handle/123456789/31458</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 02/27/2024 610 SMME-TH-796 Thesis
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