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Effects of curcumin supplementation on abdominal surgical wound healing

ABSTRACT

Purpose:

To evaluate the effects of curcumin supplementation on abdominal surgical wound healing in rats using clinical, histological, and hematological parameters.

Methods:

Forty Wistar rats were randomly divided into two groups: the curcumin group, and the control group. The curcumin group received, in addition to water and standard feed, curcumin via gavage at the dose of 200 mg/kg for seven days preceding and seven days following surgery. The control group received only water and standard feed. Both groups underwent median laparotomy and left colotomy. On the eighth postoperative day, the groups were euthanized, and the left colon was resected for histological analysis.

Results:

In the preoperative evaluation, there was a significant decrease in the mean C-reactive protein levels in the curcumin group (0.06) compared to the control group (0.112) (p = 0.0001). In the postoperative wound healing assessment, a significant decrease was observed in inflammatory infiltrate (p = 0.0006) and blood vessel count (p = 0.0002) in the curcumin group compared to the control group.

Conclusions:

Curcumin supplementation was able to significantly reduce inflammatory parameters in both pre-and post-operative phases of abdominal surgical wounds in rats.

Key words
Curcumin; Surgical Wound; Wound Healing; Rats, Wistar

Introduction

Operative wounds are classified as acute and intentionally created to prevent potential complications. However, they can also evolve in a complex manner and be considered chronic when they require a prolonged healing time. Additionally, there are different types of wound healing, categorized as primary or secondary intention. Primary intention occurs when there is no approximation of the wound edges, leading to a slower healing process. Various factors can alter the type of wound healing and pose risk factors, ranging from the patient’s own conditions to the type of surgical technique adopted. Notably, complications such as infection and dehiscence are more frequently observed11 Gillespie BM, Walker RM, McInnes E, Moore Z, Eskes AM, O’Connor T, Harbeck E, White C, Scott IA, Vermeulen H, Chaboyer W. Preoperative and postoperative recommendations to surgical wound care interventions: A systematic meta-review of Cochrane reviews. Int J Nurs Stud. 2020;102:103486. https://doi.org/10.1016/j.ijnurstu.2019.103486
https://doi.org/10.1016/j.ijnurstu.2019....
.

Wound healing is the natural process of tissue recovery following surgical trauma. It comprises three main phases: the inflammatory phase, fibroplasia, and maturation22 Balbino CA, Pereira LM, Curi R. Mecanismos envolvidos na cicatrização: uma revisão. Rev Bras Ciênc Farm. 2005;41(1):27–51. https://doi.org/10.1590/S1516-93322005000100004
https://doi.org/10.1590/S1516-9332200500...
.

The initial inflammatory phase is characterized by vasoconstriction, resulting from the release of inflammatory mediators, such as pro-inflammatory cytokines and thromboxane A2. These mediators are released by platelets adhering to the damaged and exposed endothelium. After local and natural hemostasis control, prostaglandins are released, promoting vasodilation and the migration of chemotactic molecules, attracting neutrophils and macrophages to the site of surgical trauma. Through the action of macrophages, devitalized tissues are removed, initiating the proliferation phase22 Balbino CA, Pereira LM, Curi R. Mecanismos envolvidos na cicatrização: uma revisão. Rev Bras Ciênc Farm. 2005;41(1):27–51. https://doi.org/10.1590/S1516-93322005000100004
https://doi.org/10.1590/S1516-9332200500...
,33 Medeiros AC, Dantas-Filho AM. Cicatrização das feridas cirúrgicas. J Surg Clin Res. 2016;7(2):87–102. https://doi.org/10.20398/jscr.v7i2.11438
https://doi.org/10.20398/jscr.v7i2.11438...
.

The cellular proliferation phase is a continuation of the inflammatory phase, lasting approximately 48 h to one week. Angiogenesis, fibroblast migration, stimulated by chemotactic factors released by macrophages, and epithelialization predominate in this phase. With the formation of blood vessels, originating from the migration of endothelial cells from vascular sprouts, the fibroplasia phase begins, with fibroblasts and extracellular matrix production, primarily collagen, predominating. This phase can extend from the seventh day up to three weeks. It is one of the most crucial phases, as the quantity and quality of deposited matrix will influence the scar, as well as the extension or cessation of the inflammatory phase22 Balbino CA, Pereira LM, Curi R. Mecanismos envolvidos na cicatrização: uma revisão. Rev Bras Ciênc Farm. 2005;41(1):27–51. https://doi.org/10.1590/S1516-93322005000100004
https://doi.org/10.1590/S1516-9332200500...
,33 Medeiros AC, Dantas-Filho AM. Cicatrização das feridas cirúrgicas. J Surg Clin Res. 2016;7(2):87–102. https://doi.org/10.20398/jscr.v7i2.11438
https://doi.org/10.20398/jscr.v7i2.11438...
.

The final phase is maturation, in which the quantity of fibroblasts is reduced, and myofibroblasts predominate, leading to matrix contraction, resulting from bridges between collagen fibers and the formation of a mature scar44 Tazima MDFGS, Andrade Vicente YADMV, Moriya T. Biologia da ferida e cicatrização. Med Ribeirão Preto. 2008;41(3):259–64. https://doi.org/10.11606/issn.2176-7262.v41i3p259-264
https://doi.org/10.11606/issn.2176-7262....
.

Regarding the healing process of intestinal anastomoses, fibroblasts begin to emerge during the advanced inflammatory phase and become the predominant cellular type in the wound area by the fourth day, with the proliferation phase usually extending for approximately 14 days. It is also important to differentiate that the gastrointestinal tract has differences compared to the skin, such as a broader and more diverse microbiota, which can alter the healing period55 Morgan RB, Shogan BD. The Science of Anastomotic Healing. Semin Colon Rectal Surg. 2022;33(2):100879. https://doi.org/10.1016/j.scrs.2022.100879
https://doi.org/10.1016/j.scrs.2022.1008...
.

Given this entire process, the use of curcumin is a potential aid in wound contraction, as it accelerates the phases of the healing process6. Its anti-inflammatory action is attributed to its ability to reduce inflammatory pathways, such as interleukin (IL)-1, IL-6, and transcription factors of protein I and nuclear factor kappa B (NfkB). During the proliferative phase, it is capable of increasing reepithelialization speed, as well as granulation tissue and the amount of type III collagen. In the remodeling process, there is an increase in the production of extracellular matrix components and the concentration of transforming growth factor-β (TGF-β) in the wound area, which, in turn, contributes to wound contraction77 Mohanty C, Sahoo SK. Curcumin and its topical formulations for wound healing applications. Drug Discov Today. 2017;22(10):1582–92. https://doi.org/10.1016/j.drudis.2017.07.001
https://doi.org/10.1016/j.drudis.2017.07...
.

Corroborating the potential effects on abdominal surgical wound healing, through the regulation of inflammatory signaling pathways and inhibition of inflammatory mediator synthesis, benefits in different tissues of the human body have already been demonstrated88 Peng Y, Ao M, Dong B, Jiang Y, Yu L, Chen Z, Hu C, Xu R. Anti-Inflammatory Effects of Curcumin in the Inflammatory Diseases: Status, Limitations and Countermeasures. Drug Des Devel Ther. 2021;15:4503–25. https://doi.org/10.2147/DDDT.S327378
https://doi.org/10.2147/DDDT.S327378...
. Research has shown that curcumin, due to its intrinsic properties, confers benefits in managing different inflammatory conditions, such as arthritis, psoriasis, atherosclerosis, and the systemic impacts of COVID-1999 Zeng L, Yang T, Yang K, Yu G, Li J, Xiang W, Chen H. Efficacy and Safety of Curcumin and Curcuma longa Extract in the Treatment of Arthritis: A Systematic Review and Meta-Analysis of Randomized Controlled Trial. Front Immunol. 2022;13:891822. https://doi.org/10.3389/fimmu.2022.891822
https://doi.org/10.3389/fimmu.2022.89182...
1111 Fu YS, Ho WY, Kang N, Tsai MJ, Wu J, Huang L, Weng CF. Pharmaceutical Prospects of Curcuminoids for the Remedy of COVID-19: Truth or Myth. Front Pharmacol. 2022;13:863082. https://doi.org/10.3389/fphar.2022.863082
https://doi.org/10.3389/fphar.2022.86308...
.

Based on this, this study aimed to analyze the supplementation of curcumin and, particularly, its effect on the wound healing process, evaluating hematological and clinical parameters post-left colectomy in Wistar rats.

Methods

This was an experimental study conducted at the Laboratory of Operative Technique, Prof. Gilberto Luis Ortolan, at the Universidade Estadual de Ponta Grossa, between the years 2022 and 2023. The research was conducted with approval from the Ethics Committee for Animal Use and the Brazilian Directive for Care and Use of Animals for Scientific and Educational Purposes, established by the National Council for Animal Experimentation, and followed international standards for animal experimentation (Protocol no. 23.000011573-2).

Forty male Wistar rats (Rattus norvegicus albinus, Rodentia, Mammalia) of the same lineage, weighing between 230 and 338 g, were used. These animals were obtained from the Animal Facility of the Universidade Estadual de Ponta Grossa and were housed in groups of four per cage in a climate-controlled environment (22 ± 1ºC) with controlled lighting. Throughout the experiment, they had ad libitum access to water and food.

Curcumin, the nutrient of interest, was supplemented via gavage in the pre- and post-operative period to the experimental group, seven days prior and seven days after the surgical procedure, in addition to their regular water and food. The concentration of curcumin was 200 mg/mL, administered through a size 8F gastric gavage tube, with the length of 10 cm and internal diameter of 2 mm. To formulate the curcumin solution administered via gavage, we used 1,560 mg of turmeric, with the concentration of 96% curcumin, diluted in 5 mL of glycerin and 10 mL of 0.9% saline solution. This resulted in a solution of 100 mg/mL.

All rats underwent a 12-h fasting period before the surgical procedure. This was done to minimize the presence of fecal content in the colon, making the surgical procedure easier and reducing the risks of contamination and adhesion formation. For anesthesia, intraperitoneal administration of ketamine at the dose of 40 mg/kg and xylazine at the dose of 10 mg/kg was used.

After anesthesia, the animals were weighed. Subsequently, trichotomy of the middle abdominal region was performed, and the animals were placed on the surgical table with their limbs extended. An approximately 3-cm long midline abdominal incision provided access to the abdominal cavity for exposure of the colon. The colon was sectioned 1.5 cm, at the level of the transverse and descending colon, with preservation of the colic vessels. Reconstruction was achieved by termino-terminal anastomosis in a single layer with two separate points of monofilament nylon thread, 5 cm apart. The abdominal wall was closed with anchored continuous suture of monofilament nylon 4.0 (Fig. 1) in two planes: muscle-aponeurotic, and intradermal.

Figure 1
Closure of the abdominal wall with simple suture.

After anesthetic recovery, the animals were isolated in cages and resumed ad libitum access to water and food 1 h after the procedure.

On the first postoperative day, curcumin administration was resumed. The rats were euthanized on the eighth postoperative day using an overdose of anesthetic with ketamine (160 mg/kg) and xylazine (40 mg/kg). For animal weighing, the Marte model AM 5500 scale, calibrated according to the National Institute of Metrology, Quality and Technology (INMETRO) standards, was used. Subsequently, 5 mL of blood was obtained from each specimen for biochemical analysis through a median thoracotomy and cardiac puncture in the right ventricle. After this step, the segment of the colon that underwent surgery was immersed in a 10% formalin solution for fixation, to be further used for histological study.

Statistical analysis was performed using GraphPad Prism 6, employing one-way analysis of variance (ANOVA) for multiple comparisons, followed by Tukey’s test, with the confidence interval of 95% (p ≤ 0.05). Sample size was calculated adopting a significance level of α = 0.05, for two groups of 20 animals each. The calculations were based on mean and standard deviation, establishing a test power of 90%, using the GPower 3.1.9.2 program (Fig. 2).

Figure 2
Sample size calculation in GPower 3.1.9.2.

Regarding postoperative evolution, the following aspects were evaluated: weight gain or loss, occurrence of postoperative mortality, and wound analysis. Hematocrit and C-reactive protein (CRP) levels were assessed. For this purpose, blood was collected by puncturing the vena cava during surgery and by cardiac puncture after euthanasia. Hematocrit measurement was performed by filling a capillary tube with blood up to 3/4 of its height, with one end occluded with appropriate clay. The tube was then placed in a centrifuge adjusted for 5 min at 10,000 rpm. The result was interpreted on a reading scale by observing the separation limit between erythrocyte mass and plasma.

Finally, serum was obtained by centrifuging 2 mL of blood in a refrigerated centrifuge (model NT 816 Novatechnica) for 5 min at 4,000 rpm and kept refrigerated at -20ºC until the time of analysis. Quantitative determination of CRP was performed by automated turbidimetry (selectra XL). The analytical principle was the turbidimetric method with enhanced latex. The presence of ≥ 5 mg of CRP in the sample causes agglutination of latex particles coated with anti-CRP antibodies. The degree of agglutination is proportional to the concentration of CRP in the sample. This agglutination process is based on the optical detection of very small particles suspended in liquid, forming immune complexes. The dilution becomes turbid, which is proportional to the number of antigens present in the sample.

The quantification of inflammatory cells and vessels was performed using ImageJ software–cell counter with the counting of three standardized quadrants per image. The images were obtained with an Olympus AX70 microscope, with a polarizer. To avoid variations related to the capture process, the camera settings and light intensity were identical for all samples. The images were analyzed using the ImageJ program, and the results were expressed in pixels.

For the histological study (Fig. 3), the segment of the colon that underwent surgery was used. The samples were immersed in a 10% formalin solution for fixation. After this step, dehydration, diaphanization, and tissue embedding were performed. The blocks were subjected to the microtomy process, resulting in cuts with thickness of 5 μm. These sections were stained with hematoxylin and eosin. Images of the histological slides were acquired blindly to avoid bias.

Figure 3
Standardized quadrant counting model image.

Results

Out of 40 operated rats, three deaths occurred in the control group and five in the curcumin group. Among four rats, two from the control group and two from the curcumin group, it was not possible to analyze the results due to intraoperative death. Therefore, the control group consisted of 17 rats (53.1%), and the curcumin group consisted of 15 rats (46.8%).

The average weight of the rats was 266 g with median of 262 g, ranging from a minimum of 210 g to a maximum of 338 g (Table 1). As for hematocrit, the mean value was 48.35 preoperatively and 43.5 postoperatively. In the curcumin group, the mean was 47.26 preoperatively and 42.53 postoperatively. In the control group, the mean was 49.41 preoperatively and 44.47 postoperatively, without achieving statistical significance.

Table 1
Describing weight and mortality variables, showing group homogeneity.

For CRP, the average value preoperatively was 0.094 and postoperatively it was 0.06. Comparing the two groups preoperatively, the average CRP of the control group was 0.112 and in the curcumin group it was 0.06, obtaining statistical significance (p = 0.0001). When comparing the postoperative CRP results, no statistical significance was obtained (p = 0.7861) (Table 1).

In the evaluation of postoperative wound healing, a significant decrease in inflammatory infiltrate (p = 0.0006) and blood vessel count (p = 0.0002) was found in the curcumin group compared to the control group (Figs. 4, 5, and 6).

Figure 4
Comparison of the quantity of inflammatory cells in the colon between the curcumin and control groups (Student’s t-test).
Figure 5
Comparison of the quantity of blood vessels in the colon between the curcumin and control groups (Student’s t-test).
Figure 6
Histological examination of colon segments from both the curcumin and control groups utilizing hematoxylin-eosin staining. (a and b) Curcumin group presented lower inflammatory infiltrate, number of inflammatory cells, and less blood vessels compared to (c and d) the control group.

Discussion

Surgical procedures involving the left colon have been shown to have more complications compared to those on the right side. This is attributed to anatomical differences, bacterial proliferation, the surgery itself, or other factors. Additionally, the arterial vascularization of both colons differs, resulting in different blood flow, which is greater in the right colon1212 Cazelles A, Manceau G, Maggiori L. Anatomía quirúrgica del colon. EMC Téc Quirúrgicas Apar Dig. 2023;39(1):1–9. https://doi.org/10.1016/S1282-9129(22)47399-5
https://doi.org/10.1016/S1282-9129(22)47...
,1313 Mt B, Féres O, Campos AD, Aprilli F, Rocha JJRD, Garcia RDS, Joviliano OFD. Cicatrização de anastomoses colônicas na vigência de obstrução intestinal: Estudo experimental em ratos. Acta Cir Bras. 2002;17(Suppl. 3):109–115. https://doi.org/10.1590/S0102-86502002000900023
https://doi.org/10.1590/S0102-8650200200...
. Thus, the healing process may occur differently due to the specific characteristics of each colon.

Postoperative wound complications are a significant cause of surgical complications. Marques et al.1414 Marques GS, Almeida PF, Farias LRC de, Nascimento DC do. Estudo preliminar sobre registros de deiscência de ferida operatória em um hospital universitário. Rev Hosp Univ Pedro Ernesto. 2016;15(4):312–9. https://doi.org/10.12957/rhupe.2016.31605
https://doi.org/10.12957/rhupe.2016.3160...
sought to assess the risk of wound dehiscence following surgery, concluding that impaired wound healing led to longer intensive care unit and hospital stays, as well as difficulties in mobility and bedside rest.

Numerous scientific studies have demonstrated the anti-inflammatory and antioxidant properties of curcumin, resulting in the reduction of free radicals and optimization of wound healing1515 He Y, Yue Y, Zheng X, Zhang K, Chen S, Du Z. Curcumin, inflammation, and chronic diseases: how are they linked? Mol Basel Switz. 2015;20(5):9183–213. https://doi.org/10.3390/molecules20059183
https://doi.org/10.3390/molecules2005918...
,1616 Uddin SJ, Hasan MF, Afroz M, Sarker DK, Rouf R, Islam MT, Shilpi JA, Mubarak MS. Curcumin and its Multi-target Function Against Pain and Inflammation: An Update of Pre-clinical Data. Curr Drug Targets. 2021;22(6):656–71. https://doi.org/10.2174/1389450121666200925150022
https://doi.org/10.2174/1389450121666200...
. In the present study, oral administration of curcumin via gavage demonstrated effectiveness in reducing blood vessels compared to the control group. However, it is worth noticing that the bioavailability of curcumin and its effects is lower when administered orally compared to topically1717 Cheppudira B, Fowler M, McGhee L, Greer A, Mares A, Petz L, Devore D, Loyd DR, Clifford JL. Curcumin: a novel therapeutic for burn pain and wound healing. Expert Opin Investig Drugs. 2013;22(10):1295–303. https://doi.org/10.1517/13543784.2013.825249
https://doi.org/10.1517/13543784.2013.82...
,1818 Kianvash N, Bahador A, Pourhajibagher M, Ghafari H, Nikoui V, Rezayat SM, Dehpour AR, Partoazar A. Evaluation of propylene glycol nanoliposomes containing curcumin on burn wound model in rat: biocompatibility, wound healing, and anti-bacterial effects. Drug Deliv Transl Res. 2017;7:654–63. https://doi.org/10.1007/s13346-017-0405-4
https://doi.org/10.1007/s13346-017-0405-...
.

The use of proteins as biomarkers for systemic inflammatory response is well established, with CRP being prominent due to its ease of acquisition, cost-effectiveness, and extensive literature support1919 Gabay C, Kushner I. Acute-phase proteins and other systemic responses to inflammation. N Engl J Med. 1999;340:448–54. https://doi.org/10.1056/NEJM199902113400607
https://doi.org/10.1056/NEJM199902113400...
,2020 Gorabi AM, Abbasifard M, Imani D, Aslani S, Razi B, Alizadeh S, Bagheri-Hosseinabadi Z, Sathyapalan T, Sahebkar A. Effect of curcumin on C-reactive protein as a biomarker of systemic inflammation: An updated meta- analysis of randomized controlled trials. Phytother Res PTR. 2022;36:85–97. https://doi.org/10.1002/ptr.7284
https://doi.org/10.1002/ptr.7284...
. CRP levels can rise rapidly in response to acute inflammatory conditions2121 Sato A, Oe K, Yamanaka H, Yokoyama I, Ebina K. C-reactive protein specifically enhances platelet-activating factor-induced inflammatory activity in vivo. Eur J Pharmacol. 2014;745:46–51. https://doi.org/10.1016/j.ejphar.2014.10.020
https://doi.org/10.1016/j.ejphar.2014.10...
.

In this study, a statistically significant difference was observed in CRP levels between the groups preoperatively (p < 0.05). However, in the postoperative period, no statistically significant differences were identified (p > 0.05). The nonsignificant difference in postoperative CRP may be attributed to factors such as timing, dosage, and even the surgical procedure itself. In the preoperative period, however, CRP has proven to be a response to any tissue alteration, involving complex changes spanning from the endocrine, hematologic, immune, to the neurological systems. Thus, even emotional factors may be involved in the statistically significant preoperative value obtained2222 Medeiros AC, Dantas Filho AM. Resposta metabólica ao trauma. J Surg Clin Res. 2017;8(1):56–76. https://doi.org/10.20398/jscr.v8i1.13036
https://doi.org/10.20398/jscr.v8i1.13036...
.

Regarding clinical parameters, some studies suggest that curcumin may reduce weight gain in response to increased peripheral insulin sensitivity2323 Unhapipatpong C, Polruang N, Shantavasinkul PC, Julanon N, Numthavaj P, Thakkinstian A. The effect of curcumin supplementation on weight loss and anthropometric indices: an umbrella review and updated meta-analyses of randomized controlled trials. Am J Clin Nutr. 2023;117(5):1005–16. https://doi.org/10.1016/j.ajcnut.2023.03.006
https://doi.org/10.1016/j.ajcnut.2023.03...
2525 Jin T, Song Z, Weng J, Fantus IG. Curcumin and other dietary polyphenols: potential mechanisms of metabolic actions and therapy for diabetes and obesity. Am J Physiol Endocrinol Metab. 2018;314(3):E201–E205. https://doi.org/10.1152/ajpendo.00285.2017
https://doi.org/10.1152/ajpendo.00285.20...
. However, in this study, no significant variation in weights was observed. Further comprehensive and definitive studies are warranted to explore the potential of curcumin, a promising natural bioactive, as an adjunct in combating obesity.

In this study, it was observed that Wistar rats supplemented with curcumin exhibited a significant reduction in inflammatory infiltrates and blood vessels. Additionally, there was a significant reduction in preoperative CRP levels, indicating a decrease in acute response.

For future studies, we suggest increasing the number of animals, as well as exploring variations in dosage and different methodologies, considering that curcumin has various forms of bioavailability, and topical application could be highly beneficial in the healing process. Nevertheless, further research is needed to address any remaining uncertainties.

Conclusion

Oral curcumin supplementation was able to significantly reduce inflammatory parameters in both preoperative phase (CRP) and postoperative phase (inflammatory infiltrate and blood vessel count) in abdominal surgical wounds of Wistar rats.

Acknowledgements

Not applicable.

  • Research performed at Laboratory of Operative Technique Prof. Gilberto Luis Ortolan, Universidade Estadual de Ponta Grossa, Ponta Grossa (PR), Brazil.
  • Funding

    Not applicable.

Data availability statement

All data sets were generated or analyzed in the current study.

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    » https://doi.org/10.12957/rhupe.2016.31605
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    » https://doi.org/10.3390/molecules20059183
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Edited by

Section editor: Marcus Vinicius Brito https://orcid.org/0000-0003-1476-0054

Publication Dates

  • Publication in this collection
    15 Apr 2024
  • Date of issue
    2024

History

  • Received
    06 Nov 2023
  • Accepted
    10 Feb 2024
Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia https://actacirbras.com.br/ - São Paulo - SP - Brazil
E-mail: actacirbras@gmail.com