Abstract | BACKGROUND: METHODS: We used human CSF as specimen collected during operations under spinal anesthesia. Patients were divided into three groups, patients without pain (normal group), with acute pain, and with chronic pain. We measured DPP III activities in each group, using specific substrates, such as Arg-Arg-AMC. RESULTS: DPP III activity for human CSF in patients with acute pain was significantly lower compared with that in patients without pain (P < 0.05). Furthermore, DPP III activity correlated with APN activity, another spinorphin-degrading enzyme, in patients with pain (r = 0.444). CONCLUSION: These results indicate that DPP III may play a role in regulation of endogenous opioids, leading to pain modulation.
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Authors | Hiroshi Sato, Kohei Kimura, Yukio Yamamoto, Tadahiko Hazato |
Journal | Masui. The Japanese journal of anesthesiology
(Masui)
Vol. 52
Issue 3
Pg. 257-63
(Mar 2003)
ISSN: 0021-4892 [Print] Japan |
PMID | 12703067
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- Oligopeptides
- spinorphin
- Dipeptidyl-Peptidases and Tripeptidyl-Peptidases
- dipeptidyl peptidase III
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Topics |
- Acute Disease
- Adult
- Aged
- Aged, 80 and over
- Chronic Disease
- Dipeptidyl-Peptidases and Tripeptidyl-Peptidases
(cerebrospinal fluid, physiology)
- Female
- Humans
- Male
- Middle Aged
- Oligopeptides
(metabolism)
- Pain
(enzymology)
- Reference Values
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