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Pain Management 2019 & Internal Medicine 2019

International Journal of Anesthesiology & Pain Medicine

ISSN: 2471-982X

Page 56

JOINT EVENT

7

th

Edition of International Conference on

Pain Management

8

th

Edition of International Conference on

Internal Medicine &

Patient Care

&

March 25-26, 2019

Rome, Italy

Int J Anesth Pain Med 2019, Volume 5

DOI: 10.21767/2471-982X-C1-006

Anti VEGFR therapy for osteoarthritis pain

Hee-Jeong Im Sampen

Jesse Brown Veterans Affairs Medical Center (JBVAMC) - University

of Illinois at Chicago, USA

O

steoarthritis (OA), referred as arthritis, is among the

most common chronic conditions among adults.

Osteoarthritic symptom, pain, is the key reason to seek

medical assistance, yet there is no effectiveway to relieve

OA-induced pain. Despite the major negative impact that

severe pain in chronic OA has on quality of life and health

care management, we only poorly understand origins

of pain in OA, the molecular mechanisms driving the

pathology, and theway to effectively cureOA. Many cases

eventually require joint replacement with a prosthesis

whichiscostly,andthelimitedfunctionallifeofprostheses

(~10 y) can make a second replacement necessary.

These factors increase both the overall cost of treatment

and the risk for associated morbidity. Significantly,

surgical procedures to address the condition typically do

not result in a pain-free cure. The central aim of our sutdy

is to test that the activation of Flt1 (vascular endothelial

growth factor receptor-1) is the major driver of joint pain

transmission by plasticity of peripheral (sensory neurons)

and central glial activation; Flk1 (vascular endothelial

growth factor receptor-2) is primarily responsible for

cartilage degeneration during the OA progression, thus,

simultaneous inhibition of Flt1 and Flk1 by pazopanib, an

FDA-approved small molecule anti-cancer drug, will act

as an ideal OA disease-modifying drug (OADMD) with

immediate reduction of joint pain and gradually cartilage

regeneration. The findings of our proposed research will

take the field of OA research a giant step forward: in the

short term, by increasing our mechanistic understanding

of the causes and progression of OA, and by developing

a novel strategy for treating OA and joint pain effectively

and safely in our pre-clinical OA animal model; and, in the

longer term, by providing a rationale for clinical trials to

test pazopanib to treat OA patients.

imsampen007@gmail.com