Pain Clinical Trial
Official title:
Evaluating the Relationship of Morphine Consumption and Pain-related Molecules in Hepatic Surgical Patients
According to above basic findings, it is important to confirm those results in clinic. In
this branch, the investigators will use patient control analgesic (PCA) device to investigate
the consumption of morphine for patients undergoing hepatic surgery. Preoperative and
postoperative (before and after surgery) blood will be sampling (15cc/time) and y liver
tissue (10mm3) will be harvested to measure the expression of above molecules (TM, IL-20,
HD). Pain questionnaire will also be applied to evaluate their pain control quality.
Certainly, the morphine consumption and results from pain questionnaire will be correlated
with the molecule amount to figure out possible relationship between morphine consumption and
those molecules.
Patients undergoing abdominal surgery and using morphine pain control analgesia (PCA) device
will be involved. Pre- and Post- operative (after anesthesia and at the end of surgery) blood
sampling (total 30 ml) plus normal liver tissue (10mm3) e will be harvested. Above
protein(TM, IL-20, HD) amount change will be measured (ELISA for TM, IL-20 (serum) or
flowcytometry (white cells) for TM, HD, IL-20 expression, stain or blotting for skin tissue).
Patients will be included in this branch to check the correlation between morphine
consumption and protein expression. Pain questionnaire (BPI, McGill) will be applied for pain
evaluation. 2-D gel analysis will also be applied to screen further possible molecules.
Specific aims
1. To investigate the correlation of morphine consumption and the serum amount of IL-20, TM
or HD
2. To investigate the relationship between IL-20, TM, HD amount in liver tissue and
morphine consumption
As the investigators all know, pain, as an ancient enemy to human kind, was one of the most
mystical phenomena within our body. For centuries, people search the magic wand to solve this
issue and reach the heaven destination. However, like our original sin commit by Adam and
Eve, the shadow of pain always surround and even rebel our body and spirit. Even more, pain
traps our soul and body not only for the acute stage induced by noxious stimulation but also
change our mind and body whenever chronic period start even the stimulation disappears. Pain
so far has become one of the greatest health issues for modern people. It affects millions of
people and the treatment options are quite limited and not effective everyone. Drugs for pain
relief are quite few kinds and associated with lots of side effect. On the other way, why and
how people develop chronic pain, especially when there is no further painful stimulation,
remain to be investigated. The integrated project, combining with our preliminary study and
novel findings in our university (TM, IL-20, HD), will not only set a platform for pain drug
discovery and their possible pathway in pain mechanism but also provide important clinical
data for patients with severe pain under major surgery. Four sub-projects were included in
this integrated project: 1. IL-20 is important in analgesia and pain mechanism. 2. the
potential of thrombomodulin as an analgesic. 3. Huntington mice produce less pain behavior.
4. The relationship of morphine consumption and TM, IL-20 and HD protein for post-operative
patients.
1.Interleukin-20 (IL-20) is a proinflammatory cytokine belonging to the IL-10 family. IL-20
is produced by activated keratinocytes and monocytes and transmits an intracellular signal
through two distinct cell-surface receptor complexes on keratinocytes and other epithelial
cells. IL-20 regulates proliferation and differentiation of keratinocytes during
inflammation, particularly inflammation associated with the skin. It is also involved in the
pathogenesis of osteoporosis and is a new target to treat this disease. However, little data
demonstrated its role on pain. Meanwhile, IL-10 was involved many pain models and suppresses
IL-10 expression also reduce pain in animal models. In this sub-project, Our preliminary data
demonstrated increase of IL-20 after morphine administration. Therefore, the investigators
will explore the role of IL-20 in pain management.
2.)Thrombomodulin(TM) is a transmembranous glycoprotein, thrombin mediating formation of
active protein C (APC) which involving proinflammatory and procoagulant process.
Thrombomodulin- thrombin complex activate protein C and inhibits coagulation cascade.
Lectin-like domain (D1) of TM prevents neutrophil and monocyte adhesion with inhibiting
inflammation process. In addition, TM bind with HMGB1 (high-mobility group box 1) and prevent
leukocyte activation demonstrated in previous study. HMGB1 appears to have a role in
neuropathic pain involving dorsal root ganglion and peripheral nerve injury in recent
investigations and develop many therapies aim to HMGB1 including antibody in recent days.
HMGB1 interact with RAGE and related to induce hyperalgesia in a rodent model of neuropathic
pain and pain hypersensitivity after peripheral nerve injury. In this branch study, the
investigators will use various pain models to evaluate the expression of TM in tissues.
3.Huntington disease(HD) is neurodegenerative genetic disorder that affects muscle
coordination. It caused by autosomal dominant mutation in Huntingtin gene and accumulates
Huntington protein. This protein plays an important role in nerve cells. It upregulates Brain
Derived Neurotrophic Factor (BDNF) and essential for development. It is associated with
vesicles and microtubules and involved in vesicle trafficking. It also interact with over 100
other protein. However, less investigation focuses this protein on pain sensory level. Under
the cooperation of Dr. Yang, the investigators will investigate the over-expression
Huntington protein mice that will induce Huntington disease. The investigators will work on
this issue and deepen our finding and produce a new view for this old disease.
4.According to above basic findings, it is important to confirm those results in clinic. In
this branch, the investigators will use the patient control analgesic (PCA) device to
investigate the consumption of morphine for patients undergoing hepatic surgery. Preoperative
and postoperative blood will be sampling and tinny liver tissue (10mm3) will be harvested to
correlate their morphine consumption and pain questionnaire will be evaluated for their pain
control quality. Certainly, the morphine consumption will be correlated with the molecule
amount to figure out possible relationship between morphine consumption and those molecules.
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