Browse > Article
http://dx.doi.org/10.3344/kjp.2019.32.3.168

Diverse characters of Brennan's paw incision model regarding certain parameters in the rat  

Kumar, Rahul (Department of Anatomy, All India Institute of Medical Sciences)
Gupta, Shivani (Department of Anatomy, All India Institute of Medical Sciences)
Gautam, Mayank (Department of Anatomy, All India Institute of Medical Sciences)
Jhajhria, Saroj Kaler (Department of Anatomy, All India Institute of Medical Sciences)
Ray, Subrata Basu (Department of Anatomy, All India Institute of Medical Sciences)
Publication Information
The Korean Journal of Pain / v.32, no.3, 2019 , pp. 168-177 More about this Journal
Abstract
Background: Brennan's rodent paw incision model has been extensively used for understanding mechanisms underlying postoperative pain in humans. However, alterations of physiological parameters like blood pressure and heart rate, or even feeding and drinking patterns after the incision have not been documented as yet. Moreover, though eicosanoids like prostaglandins and leukotrienes contribute to inflammation, tissue levels of these inflammatory mediators have never been studied. This work further investigates the antinociceptive effect of protein C after intra-wound administration. Methods: Separate groups of Sprague-Dawley rats were used for quantitation of cyclooxygenase (COX) activity and leukotriene B4 level by enzyme-linked immunosorbent assay, as well as estimation of cardiovascular parameters and feeding and drinking behavior after paw incision. In the next part, rats were subjected to incision and $10{\mu}g$ of protein C was locally administered by a micropipette. Both evoked and non-evoked pain parameters were then estimated. Results: COX, particularly COX-2 activity and leukotriene B4 levels increased after incision. Hemodynamic parameters were normal. Feeding and drinking were affected on days 1 and 3, and on day 1, respectively. Protein C attenuated non-evoked pain behavior alone up to day 2. Conclusions: Based upon current observations, Brennan's rodent paw incision model appears to exhibit a prolonged period of nociception similar to that after surgery, with minimal interference of physiological parameters. Protein C, which is likely converted to activated protein C in the wound, attenuated the guarding score, which probably represents pain at rest after surgery in humans.
Keywords
Blood Pressure; Eicosanoids; Heart Rate; Inflammation; Nociception; Pain, Postoperative; Protein C; Rats; Wounds and Injuries;
Citations & Related Records
Times Cited By KSCI : 1  (Citation Analysis)
연도 인용수 순위
1 Xu J, Brennan TJ. The pathophysiology of acute pain: animal models. Curr Opin Anaesthesiol 2011; 24: 508-14.   DOI
2 Wu C, Boustany L, Liang H, Brennan TJ. Nerve growth factor expression after plantar incision in the rat. Anesthesiology 2007; 107: 128-35.   DOI
3 Kim TJ, Freml L, Park SS, Brennan TJ. Lactate concentrations in incisions indicate ischemic-like conditions may contribute to postoperative pain. J Pain 2007; 8: 59-66.   DOI
4 Gautam M, Prasoon P, Kumar R, Reeta KH, Kaler S, Ray SB. Role of neurokinin type 1 receptor in nociception at the periphery and the spinal level in the rat. Spinal Cord 2016; 54: 172-82.   DOI
5 Foster D, Dav ie EW. Characterization of a cDNA coding for human protein C. Proc Natl Acad Sci U S A 1984; 81: 4766-70.   DOI
6 Joyce DE, Gelbert L, Ciaccia A, DeHoff B, Grinnell BW. Gene expression profile of antithrombotic protein c defines new mechanisms modulating inflammation and apoptosis. J Biol Chem 2001; 276: 11199-203.   DOI
7 Kumar R, Prasoon P, Gautam M, Ray SB. Comparative antinociceptive effect of arachidonylcyclopropylamide, a cannabinoid 1 receptor agonist & lignocaine, a local anaesthetic agent, following direct intrawound administration in rats. Indian J Med Res 2016; 144: 730-40.   DOI
8 Bauer KA, Kass BL, Beeler DL, Rosenberg RD. Detection of protein C activation in humans. J Clin Invest 1984; 74: 2033-41.   DOI
9 Long GL, Belagaje RM, MacGillivray RT. Cloning and sequencing of liver cDNA coding for bovine protein C. Proc Natl Acad Sci U S A 1984; 81: 5653-6.   DOI
10 Esmon CT. The endothelial cell protein C receptor. Thromb Haemost 2000; 83: 639-43.   DOI
11 Marlar RA, Kleiss AJ, Griffin JH. Mechanism of action of human activated protein C, a thrombin-dependent anticoagulant enzyme. Blood 1982; 59: 1067-72.   DOI
12 Xue M, Thompson P, Kelso I, Jackson C. Activated protein C stimulates proliferation, migration and wound closure, inhibits apoptosis and upregulates MMP-2 activity in cultured human keratinocytes. Exp Cell Res 2004; 299: 119-27.   DOI
13 Bernard GR, Vincent JL, Laterre PF, LaRosa SP, Dhainaut JF, Lopez-Rodriguez A, et al. Efficacy and safety of recombinant human activated protein C for severe sepsis. N Engl J Med 2001; 344: 699-709.   DOI
14 Yuksel M, Okajima K, Uchiba M, Horiuchi S, Okabe H. Activated protein C inhibits lipopolysaccharide-induced tumor necrosis factor-alpha production by inhibiting activation of both nuclear factor-kappa Band activator protein-1 in human monocytes. Thromb Haemost 2002; 88: 267-73.   DOI
15 Xue M, March L, Sambrook PN, Jackson CJ. Differential regulation of matrix metalloproteinase 2 and matrix metalloproteinase 9 by activated protein C : relevance to inflammation in rheumatoid arthritis. Arthritis Rheum 2007; 56: 2864-74.   DOI
16 Smith JR, Galie PA, Slochower DR, Weisshaar CL, Janmey PA, Winkelstein BA. Salmon-derived thrombin inhibits development of chronic pain through an endothelial barrier protective mechanism dependent on APC. Biomaterials 2016; 80: 96-105.   DOI
17 Pichler L, Schramm W, Ulrich W, Varadi K, Schwarz HP. Antinociceptive properties of protein C in a model of inflammatory hyperalgesia in rats. Thromb Haemost 1995; 73: 252-5.   DOI
18 Zimmermann M. Ethical guidelines for investigations of experimental pain in conscious animals. Pain 1983; 16: 109-10.   DOI
19 Brennan TJ, Vandermeulen EP, Gebhart GF. Characterization of a rat model of incisional pain. Pain 1996; 64: 493-501.   DOI
20 Wijewardena A, Lajevardi SS, Vandervord E, Vandervord J, Lang TC, Fulcher G , et al. Activated protein C to heal pressure ulcers. Int Wound J 2016; 13: 986-91.   DOI
21 Brown C, McFarlane-Anderson N, Alexander-Lindo R, Bishop K, Dasgupta T, McGrowder D. The effects of S-nitrosoglutathione and S-nitroso-N-acetyl-D, L-penicillamine in a rat model of pre-eclampsia. J Nat Sci Biol Med 2013; 4: 330-5.   DOI
22 Wang Y, Cong Y, Li J, Li X, Li B, Qi S. Comparison of invasive blood pressure measurements from the caudal ventral artery and the femoral artery in male adult SD and Wistar rats. PLoS One 2013; 8: e60625.   DOI
23 Spofford CM, Ashmawi H, Subieta A, Buev ich F, Moses A, Baker M, et al. Ketoprofen produces modality-specific inhibition of pain behaviors in rats after plantar incision. Anesth Analg 2009; 109: 1992-9.   DOI
24 Chaplan SR, Bach FW, Pogrel JW, Chung JM, Yaksh TL. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods 1994; 53: 55-63.   DOI
25 Hargreaves K, Dubner R, Brown F, Flores C, Joris J. A new and sensitive method for measuring thermal nociception in cutaneous hyperalgesia. Pain 1988; 32: 77-88.   DOI
26 Pogatzki-Zahn EM, Segelcke D, Schug SA. Postoperative pain-from mechanisms to treatment. Pain Rep 2017; 2: e588.   DOI
27 Braz JM, Etlin A, Juarez-Salinas D, Llewellyn-Smith IJ, Basbaum AI. Rebuilding CNS inhibitory circuits to control chronic neuropathic pain and itch. Prog Brain Res 2017; 231: 87-105.   DOI
28 Rouzer CA, Marnett LJ. Cyclooxygenases: structural and functional insights. J Lipid Res 2009; 50 Suppl: S29-34.   DOI
29 Lavand'homme P, Wu C, Katz J. From acute to chronic postoperative pain. In: Pain 2018: refresher courses for the 17th World Congress on Pain. Edited by Gold MS, Pogatzki-Zahn EM, Wallace MS. Washington, IASP Press. 2018, pp 147-57.
30 Polanco-Garcia M, Garcia-Lopez J, Fabregas N, Meissner W, Puig MM; PAIN-OUT-Spain Consortium. Postoperative pain management in Spanish hospitals: a cohort study using the pain-out registry. J Pain 2017; 18: 1237-52.   DOI
31 Smith WL, DeWitt DL, Garavito RM. Cyclooxygenases: structural, cellular, and molecular biology. Annu Rev Biochem 2000; 69: 145-82.   DOI
32 Futagami A, Ishizaki M, Fukuda Y, Kawana S, Yamanaka N. Wound healing involves induction of cyclooxygenase-2 expression in rat skin. Lab Invest 2002; 82: 1503-13.   DOI
33 Koller M, Konig W, Brom J, Raulf M, Gross-Weege W, Erbs G, et al. Generation of leukotrienes from human polymorphonuclear granulocytes of severely burned patients. J Trauma 1988; 28: 733-40.   DOI
34 Cunha JM, Sachs D, Canetti CA, Poole S, Ferreira SH, Cunha FQ. The critical role of leukotriene B4 in antigen-induced mechanical hyperalgesia in immunised rats. Br J Pharmacol 2003; 139: 1135-45.   DOI
35 Guimaraes FR, Sales-Campos H, Nardini V, da Costa TA, Fonseca MTC, Junior VR, et al. The inhibition of 5-Lipoxygenase (5-LO) products leukotriene B4 ($LTB_4$) and cysteinyl leukotrienes (cysLTs) modulates the inflammatory response and improves cutaneous wound healing. Clin Immunol 2018; 190: 74-83.   DOI
36 Fujita M, Fukuda T, Sato Y, Takasusuki T, Tanaka M. Allopregnanolone suppresses mechanical allodynia and internalization of neurokinin-1 receptors at the spinal dorsal horn in a rat postoperative pain model. Korean J Pain 2018; 31: 10-5.   DOI
37 Foo H, Crabtree K, Thrasher A, Mason P. Eating is a protected behav ior even in the face of persistent pain in male rats. Physiol Behav 2009; 97: 426-9.   DOI
38 Hackett AF, Yeung CK, Hill GL. Eating patterns in patients recovering from major surgery--a study of voluntary food intake and energy balance. Br J Surg 1979; 66: 415-8.   DOI
39 Brennan TJ. Pathophysiology of postoperative pain. Pain 2011; 152(3 Suppl): S33-40.   DOI
40 Deane R, LaRue B, Sagare AP, Castellino FJ, Zhong Z, Zlokovic BV. Endothelial protein Creceptor-assisted transport of activated protein Cacross the mouse blood-brain barrier. J Cereb Blood Flow Metab 2009; 29: 25-33.   DOI
41 Carney EF. Inflammation: activated protein C inhibits inflammasome activation in IRI. Nat Rev Nephrol 2017; 13: 662.   DOI
42 Riewald M, Petrovan RJ, Donner A, Ruf W. Activated protein C signals through the thrombin receptor PAR1 in endothelial cells. J Endotoxin Res 2003; 9: 317-21.   DOI
43 Toltl LJ, Austin RC, Liaw PC. Activated protein C modulates inflammation, apoptosis and tissue factor procoagulant activity by regulating endoplasmic reticulum calcium depletion in blood monocytes. J Thromb Haemost 2011; 9: 582-92.   DOI
44 Comp PC, Nixon RR, Esmon CT. Determination of functional levels of protein C, an antithrombotic protein, using thrombinthrombomodulin complex. Blood 1984; 63: 15-21.   DOI
45 Funk CD. Prostaglandins and leukotrienes: advances in eicosanoid biology. Science 2001; 294: 1871-5.   DOI
46 Kumar V, Abbas AK, Aster JC. Robbins basic pathology. Philadelphia, Elsevier. 2013, pp 29-73.
47 Dubois RN, Abramson SB, Crofford L, Gupta RA, Simon LS, Van De Putte LB, et al. Cyclooxygenase in biology and disease. FASEB J 1998; 12: 1063-73.   DOI