Therapeutic Application of Crude Mitochondrial Transplantation for Diabetic Wound Healing / (Record no. 614596)

000 -LEADER
fixed length control field 02221nam a22001577a 4500
082 ## - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 610
100 ## - MAIN ENTRY--PERSONAL NAME
Personal name Hameed, Farhan
245 ## - TITLE STATEMENT
Title Therapeutic Application of Crude Mitochondrial Transplantation for Diabetic Wound Healing /
Statement of responsibility, etc. Farhan Hameed
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 77p.
Other physical details Soft Copy
Dimensions 30cm
500 ## - GENERAL NOTE
General note Chronic wounds in diabetic condition pose a persistent clinical challenge, primarily due<br/>to impaired cellular energy metabolism and delayed tissue regeneration. Mitochondrial<br/>dysfunction plays pivotal role in this impaired healing process, making mitochondrial<br/>transplantation (MT) a promising therapeutic strategy. This study investigates the<br/>efficacy of MT in accelerating wound repair using a diabetic mice model. Full-thickness<br/>excisional wounds (6mm) were created on the dorsal surface of diabetic mice, followed<br/>by subcutaneous administration of isolated crude mitochondria at low, moderate and<br/>high dose (5ug, 10ug, and 20ug) mitochondria per wound. A vehicle-treated group<br/>receiving phosphate-buffered saline (PBS) served as the control.<br/>Mitochondrial viability and quantification were assessed using MTT assay and Bradford<br/>in wound contraction. Wound closure analysis revealed a dose-dependent acceleration of<br/>healing, with high-dose group exhibiting the most significant improvement in wound<br/>contraction and re-epithelialization. Histological analysis confirmed enhanced tissue<br/>regeneration in the treatment groups. Furthermore real-time PCR analysis demonstrated a<br/>significant upregulation of RAC1, CDC42, and VEGF in the moderate and high treatment<br/>groups, indicating enhanced cytoskeletal remodeling, cellular migration and<br/>angiogenesis.<br/>These findings highlight the therapeutic potential of crude mitochondrial transplantation<br/>in diabetic wound healing by restoring cellular bioenergetics and promoting tissue repair.<br/>This approach offers a promising regenerative strategy for managing chronic wound and<br/>improving diabetic wound outcomes.
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. Hussain Mustatab Wahedi
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="http://10.250.8.41:8080/xmlui/handle/123456789/54551">http://10.250.8.41:8080/xmlui/handle/123456789/54551</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 08/29/2025 610 SMME-TH-1152 Thesis
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