The Korean Journal of Pain 2019; 32(4): 256-263
Published online October 1, 2019 https://doi.org/10.3344/kjp.2019.32.4.256
Copyright © The Korean Pain Society.
Ahmed Abdullah Elberry1 , Souty Mouner Zaky Sharkawi2
, and Mariam Rofaiel Wahba1
1Department of Pharmacology, Faculty of Medicine, Beni-Suef University, Beni-Suef, Egypt
2Department of Pharmacology and Toxicology, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, Egypt
Correspondence to:Ahmed Abdullah Elberry
Department of Pharmacology, Faculty of Medicine, Beni-Suef University, Built Salah Salem Street, Beni-Suef 62511, Egypt
Tel: +20-236533024
Fax: +20-822318605
E-mail: berry_ahmed@yahoo.com
Received: February 19, 2019; Revised: July 6, 2019; Accepted: July 11, 2019
This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Antinociceptive anti-inflammatory drugs have many adverse effects. The goal of this investigation is to study the probable anti-inflammatory and analgesic effects of verapamil and N-acetylcysteine (NAC) in experimental rats. Adult male Wistar rats were randomly divided into 4 groups in the antinociceptive study, each containing 6 rats; the normal control group, which received saline (1 mL/kg); the diclofenac group, which received diclofenac sodium (5 mg/kg); the NAC group, which received NAC (125 mg/kg); and the verapamil group, which received verapamil (8 mg/kg). In the anti-inflammatory study, 5 groups were used, the 4 previous groups with the addition of an edema control group, received saline and were subjected to formalin test. Hot plate latency time was recorded for antinociceptive evaluation. Paw edema thickness and biochemical parameters were recorded for anti-inflammatory evaluation. Administration of NAC showed significant prolongation of hot plate latency time at 1 hour when compared to the control group while verapamil showed a significant prolongation of hot plate latency time at 1 and 2 hours when compared to the control group and NAC group values. Administration of NAC and verapamil significantly decreased paw edema thickness at 2, 4, and 8 hours when compared to edema control values. Regarding biochemical markers, NAC and verapamil significantly decreased serum nitric oxide synthase, C-reactive protein, and cyclooxygenase-2 levels compared to the edema control value. In accordance, a marked improvement of histopathological findings was observed with both drugs. NAC and verapamil have antinociceptive and anti-inflammatory effects comparable to diclofenac sodium.Background
Methods
Results
Conclusions
Keywords: Anti-Inflammatory Agents, Antinociceptive, Cyclooxygenase 2, Diclofenac, Edema, Nitric Oxide Synthase, Pain Measurement, Verapamil
Pain and inflammation are common manifestations of many diseases. Pain is an unpleasant, sensory and emotional experience associated with actual or potential tissue damage, and originates from inflammation and the inflammatory responses [1]. Inflammation is a nonspecific response that has a beneficial effect on the host. Several experimental studies have shown that reactive oxygen species (ROS) contribute to pain [2]. Proinflammatory cytokines including tumor necrosis factor (TNF)-α play significant roles in neuronal reaction and inflammation [3]. Nonsteroidal anti-inflammatory drugs, such as diclofenac, are the most commonly used antinociceptive and antiinflammatory drugs, since they are effective in the management of pain, fever, redness, and edema resulting from inflammatory mediator release [4]. Although diclofenac is usually well tolerated by patients, its use is associated with some adverse drug reactions, such as gastrointestinal mucosal damage, renal toxicity, bleeding, and cardiovascular side effects [5].
Finding different types of drugs to induce the same antiinflammatory and antinociceptive effects with fewer side effects became a priority. N-acetylcysteine (NAC) acts both as a glutathione (GSH) precursor and shows anti-inflammatory and antioxidant effects [6]. By regulation of the redox status in the cell, it can interfere with several signaling pathways and decrease the cytokine production in the early inflammatory response [7]. Verapamil belongs to the dihydropyridine family of calcium channel blockers that block voltage-dependent L-type calcium channels, and is used clinically to treat hypertension, angina, and cardiac arrhythmias [8]. Previous studies have also found that verapamil inhibits activation of superoxide production in neutrophils and macrophages [9]. Increased calcium influx through L-type calcium channels causes activation of signaling cascades, such as ROS and activation of proinflammatory cytokines [10]. Previous studies showed that verapamil elicited neuroprotection action and has a significant anti-inflammatory and anti-angiogenesis effects [11]. The aim of the present work was to study the probable anti-inflammatory and antinociceptive effects of verapamil and NAC in rats.
Diclofenac sodium (Diclac 75 mg; Minapharm, Giza, Egypt), NAC (Acetylcysteine 600 mg; SEDICO, Cairo, Egypt), verapamil (Isoptin 80 mg; Kahira Pharmaceuticals & Chemical Industries Company, Cairo, Egypt), isotonic saline (Otsuka Pharmaceutical Company, Cairo, Egypt), and formalin (Formaldehyde sol. 38%–40%; Al-Nasr Pharma Chemicals, Cairo, Egypt) were used in the current study.
Experiments were performed on adult male Wistar rats weighing 220 to 280 g in accordance with the guidelines of the Ethics Committee at Beni-Suef University (# 018-63), which complies with Guidelines on Ethical Standards for Investigation of Experimental Pain in Animals [12]. The animals were housed and maintained in a well ventilated, temperature-controlled room at 22°C ± 2°C with a relative humidity of 50% to 60% and a 12-hour light-dark cycle with free access to food and water. They were acclimatized for 1 week and randomly allocated into groups. Care was taken to avoid stressful conditions and to minimize animal suffering, and all experimental procedures were performed between 9 and 11 am. All drugs were administered orally using a metallic tube, and the rat was forced to swallow them one hour before the hot plate or formalin test.
The rats were divided randomly into 4 groups, 6 rats in each group; the normal control group received saline (1 mL/kg), the diclofenac group received diclofenac sodium (2 mg/ kg) [13], the NAC group received NAC (150 mg/kg) [14], and the verapamil group received verapamil (8 mg/kg) [15].
The hot plate method was used to investigate the nociception in rats as described by Langerman et al. [16]. Each rat was placed in a hot plate analgesia meter (TSE Systems, Bad Homburg vor der Höhe, Germany) and the metal surface was maintained at 50°C ± 1°C. The latency times in seconds taken to nocifensive behavior including hind paw withdrawal or licking, and jumping was recorded prior to the treatment, 1, and 2 hours after the treatment [17]. Rats showing a pretreatment reaction time greater than 30 seconds in the hot plate test were excluded from the experiment (cut-off latency) [18].
The rats were divided randomly into 5 groups as in 4 groups in the hot plate test in addition to a paw edema group. The normal control group received saline (1 mL/ kg), the paw edema control received saline (1 mL/kg), the diclofenac group received diclofenac sodium (2 mg/kg) [13], the NAC group received NAC (150 mg/kg) [14], and verapamil group received verapamil (8 mg/kg) [15]. Compounds were administered
Blood samples (up to 2 mL) were collected by orbital puncture under inhalation anesthesia using alcohol, chloroform, and ether in a ratio of 1:2:3. In serum separating tubes, the blood samples were centrifuged at 3,000 rpm for 15 minutes to separate the sera and were stored at 80°C for biochemical analyses [20]. Reduced GSH and myeloperoxidase (MPO) were determined according to standard methods using diagnostic kits from BioSystems S.A. (Barcelona, Spain). Assessment of serum TNF-α, inducible nitric oxide synthetase (iNOS), cyclooxygenase enzyme (COX-2), and C-reactive protein (CRP) were carried out by enzymelinked immunosorbent assay (ELISA) using kit purchased from DRG International Inc. (Mountainside, NJ).
After collection of blood samples, all animals were euthanized. The right and left paws were dissected from the rats and kept intact for histological examination and the soft tissues of paw were isolated carefully. Paw tissues were fixed immediately and decalcified in ethylenediaminetetraacetic acid [21]. Then, the tissue specimens were dehydrated, embedded in paraffin, and sectioned into 5 μm portions, and stained using hematoxylin and eosin (H&E) for histopathological examination using a research microscope provided with an HD camera (Leica DM2500 M; Leica Microsystems GmbH, Wetzlar, Germany). A histopathologic score is used for inflammation, congestion, and edema on a 7-grade scale from 0 to 6 (0 = normal and 6 = the most severe inflammation).
Data were expressed for each parameter investigated as a mean ± standard error of the mean. One-way analysis of variance (ANOVA) was used to compare the different groups. All statistics were carried out using SPSS ver. 15 (SPSS Inc., Chicago, IL). Differences were considered statistically significant when the
The present study showed that administration of a single dose of NAC produced a significant prolongation of the hot plate latency time at 1 hour after treatment when compared to the normal control group values. Moreover, administration of a single dose of verapamil showed a significant prolongation of the hot plate latency time at 1 and 2 hours after treatment, which is comparable to diclofenac group values (Table 1).
The present study revealed that administration of NAC and verapamil significantly decreased paw edema thickness at 2, 4, and 8 hours when compared to edema control values. Both NAC and verapamil decreased paw edema thickness to the same values of diclofenac at 2 and 8 hours (Fig. 1).
The current investigation showed that formalin-induced paw edema significantly decreased the serum levels of GSH, while TNF-α, MPO, NOS, CRP, and COX-2 increased significantly when compared to normal control values. The alterations in NOS, CRP, COX-2, and TNF-α were alleviated significantly when compared to paw edema values (Table 2, Fig. 2).
On the other hand, verapamil decreased significantly the elevated MPO level when compared with the paw edema value, while NAC decreased this elevation, but nonsignificantly. Moreover, diclofenac, NAC, and verapamil failed to alleviate the serum GSH level (Table 2).
Histopathological examination of the hind paw of the normal control rats showed normal dermal and epidermal architecture with no signs of inflammation (Fig. 3A). On injection of formalin, the histopathological study revealed severe inflammation evidenced by mononuclear infiltration of inflammatory cells, severe edema, mild congestion, and the highest score (Fig. 3B). On the other hand, injection of diclofenac sodium ameliorated the edema, inflammation, and congestion and ameliorated the histopathological scoring (Figs. 3A, 3D, 4). Rats which received NAC (Fig. 3E, F) and verapamil (Fig. 3G, H) showed low histopathological scoring and mild inflammation evidenced by subsiding edema and fewer inflammatory cells with less congestion and presence of macrophages that engulf debris with necrosed tissue (Fig. 3G, H).
The hot plate test and other tests that apply heat stimuli to the hind paws are considered to integrate supraspinal pathways, as rats with spinal transection do not withdraw the hind limbs in the hot plate test [22]. The results of the present study revealed that NAC has an antinociceptive effect evidenced by a significant prolongation of hot plate latency time when compared to normal control values. Despite that, NAC significantly prolonged the hot plate latency time when compared to normal control values but this prolongation was less than that of diclofenac sodium values. These results are in agreement with Horst et al. [23] who reported that NAC has an anti-hyperalgesic effect in rats with neuropathic pain mostly attributed to modulation of the antioxidant redox system, reduction in several neuroinflammatory molecules, and a decrease in nitric oxide (NO). Similarly, the current study showed that verapamil produced a significant prolongation of hot plate latency time when compared to normal control values and the NAC group but still inferior to diclofenac sodium group values. These results are in agreement with Abdollahi et al. [24] who reported that verapamil induced a significant anti-nociception in both phases of a formalin test model. Verapamil, a calcium channels blocker, resulted in impaired calcium influx, a necessary process for activation of N-methyl-D-aspartate receptors of glutamate which induces the local release of both prostaglandin E2 (PGE2) and NO, thereby relieving pain [24].
On the other hand, formalin significantly increased paw edema thickness in the present study after 1, 2, 4, and 8 hours, which is in agreement with the results of Lee and Jeong [25]. This edema is mainly caused by vascular changes which are mediated by release of substance P, prostanoids, 5-hydroxytryptamine, and histamine [26]. The present study showed that NAC significantly alleviated paw edema thickness after 2, 4, and 8 hours, which is in agreement with the results of Lasram et al. [27] and Farshid et al. [28]. Moreover, the present study showed that verapamil produced a statistically significant alleviation in paw edema thickness after 2, 4, and 8 hours. This result is in agreement with the results of Martinez et al. [29].
The alleviation by NAC was be explained in previous studies by reduction of neutrophil infiltration and inhibition of COX products such as prostaglandins, and also
Despite both NAC and verapamil showing a significant anti-inflammatory effect compared to the edema control group, neither NAC nor verapamil was superior to diclofenac in ameliorating paw edema after 2 and 4 hours. However, after 8 hours the ameliorative effect of both NAC and verapamil on paw edema thickness values was nearly the same as that of diclofenac values. Unfortunately, the results of the present study showed that diclofenac, NAC, and verapamil failed to improve the decreased level of GSH in the edema control group. This can be explained by the short duration of the experiment and nonspecific method that is used in the current study, as GSH was measured in plasma and not tissues.
In the current study, treatment with either diclofenac or NAC failed to produce any significant ameliorative effect on the increased level of MPO in the edema control group. The diclofenac effect in the present study is in agreement with the previous results of Pireddu et al. [31]. On the other hand, verapamil significantly ameliorated the increased serum MPO level when compared to the edema control group and decreased it to nearly the normal control values. These results are in agreement with the results of Messiha and Abo-Youssef [32]. This could be attributed to its calcium channel blocking activity in addition to attenuation of chemo-attractant release by Kupffer cells [33].
Huang et al. [34], showed similar results regarding the effect of NAC on COX expression. On the other hand, Wang et al. [35] reported that verapamil significantly inhibited COX-2 level in inflammatory arthritis in mice, which could be explained, since Ca2+ influx leads to the up-regulation of COX-2 expression and PGE2 release
Regarding to the findings of the present work, NAC, verapamil, and diclofenac significantly reduced the elevated serum NOS level observed in the edema control group. There was no significant difference between the three groups. Guibas et al. [42] showed that NAC significantly inhibited the accumulation of inflammatory cells and down regulated iNOS expression in a rat model of allergic rhinitis. The effect of NAC on NOS can be attributed mostly to the inhibitory effect of NAC on one of the events leading to iNOS protein expression [43]. The effect of verapamil on NOS in the present results may be due to inhibition of inflammatory cytokines [10].
Regarding the findings of the present work, NAC, verapamil, and diclofenac sodium significantly reduced the elevated serum CRP level observed in the edema control group. There was no significant difference between the 3 groups. The results of the present study regarding the NAC group are in agreement with Saddadi et al. [44].
The NAC was shown to inhibit the production of interleukin (IL)-6 from macrophages which is related to the anti-oxidative stress effects of NAC [45]. Since CRP increases following IL-6 secretion by macrophages and T cells, NAC results regarding CRP can be explained by its effect on IL-6 [46]. Bakris [47] reported that verapamil significantly reduced CRP and lowered albuminuria in kidney disease progression. The effect of verapamil on CRP may be because it can modulate T-helper cell type 2 associated cytokine secretion, such as IL-5 and IL-6 [48] which stimulate hepatic secretion of CRP following IL-6 secretion by macrophages and T cells [46].
In conclusion, NAC and Verapamil were found to have antinociceptive and anti-inflammatory effects. This antinociceptive effect can be attributed to COX inhibition and an antioxidant effect. Further clinical and long-term studies are needed to confirm their clinical effectiveness and safety.
The Effect of N-acetylcysteine and Verapamil on Hot Plate Latency Time in Rats
Variable | Latency time (sec) | ||
---|---|---|---|
Pre-treatment | Post-treatment | ||
1 hr | 2 hr | ||
Normal control | 15.00 ± 0.41 | 16.00 ± 0.25 | 16.00 ± 0.65 |
Diclofenac | 16.00 ± 0.82 | 29.00 ± 1.50a | 27.00 ± 1.10a |
Values are presented as mean ± standard error of the mean (6 rats in each group).
aSignificantly different from normal control value.
The Effect of 2 Doses of Diclofenac Sodium, N-acetylcysteine and Verapamil on the Formalin-Induced Paw Edema Serum Alterations of Reduced GSH, TNF-α, MPO, NOS
Variable | GSH (mg/dL) | TNF-α (mg/dL) | MPO (mg/dL) | NOS (mg/dL) |
---|---|---|---|---|
Normal control | 67.48 ± 1.16 | 20.98 ± 1.88 | 2.22 ± 0.24 | 10.30 ± 0.76 |
Paw edema | 33.28 ± 5.17a | 97.48 ± 6.02a | 7.46 ± 1.84a | 33.04 ± 5.39a |
Values are presented as mean ± standard error of the mean (6 rats in each group).
GSH: glutathione, TNF-α: tumor necrosis factor-alpha, MPO: myeloperoxidase, NOS: nitric oxide synthase.
aSignificantly different from normal control value.