<i>Cuscuta reflexa</i> Roxb. Expedites the Healing Process in Contact Frostbite

Hassan, Waseem; Buabeid, Manal Ali; Kalsoom, Umme; Bakht, Sahar; Akhtar, Imran; Iqbal, Furqan; Arafa, El-Shaimaa A.

doi:https://doi.org/10.1155/2020/4327651

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Abstract Introduction Materials and Methods Results Discussion Conclusion Data Availability Conflicts of Interest Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 4327651 | https://doi.org/10.1155/2020/4327651

Cuscuta reflexa Roxb. Expedites the Healing Process in Contact Frostbite

Waseem Hassan,¹Manal Ali Buabeid,²Umme Kalsoom,³Sahar Bakht,³Imran Akhtar,³Furqan Iqbal,⁴and El-Shaimaa A. Arafa^2,5

Academic Editor: Maxim E. Darvin

Received23 Oct 2019

Revised19 Feb 2020

Accepted07 Jul 2020

Published05 Oct 2020

Abstract

Frostbite is caused due to extreme vulnerability to cold, resulting in damage of deeper and superficial tissues alike. In this study, we report the anti-inflammatory and wound-healing properties of aqueous methanolic extract of Cuscuta reflexa (Cs.Cr) against contact frostbite. Thirty rats were divided into five groups including three treatment groups with increasing doses of Cs.Cr, a standard drug group receiving acetylsalicylic acid (ASA), and a metal bar-induced frostbite group. Frostbite injury was induced by a cm metal bar frozen up to -79°C on shaved skin for continuous 3 minutes. Wounded area percentages were recorded to measure the healing rate in response to Cs.Cr administration. Haematological parameters and malondialdehyde content were also noted. On treatment with Cs.Cr, the healing rate is drastically increased and lipid peroxidation product malondialdehyde was decreased in a dose-dependent manner. Results were compared with frostbite and ASA (standard drug group). These results indicate that Cs.Cr possesses excellent wound-healing properties against frostbite injury and can prove to be a prospective compound in such conditions.

1. Introduction

Frostbite is an injury caused by freezing of the skin and underlying tissues commonly caused by exposure to cold-weather conditions and contact with ice, freezing metal, or cold liquids. It represents a continuum of tissue injuries, ranging from superficial insult to deep tissue damage [1]. Although a comprehensive epidemiological study is yet to be surfaced, it is estimated that 366 out of 1000 mountaineers suffer frostbite per year [2]. It is assessed that men in the age bracket of 30-49 are most at risk of frostbite due to greater chances of exposure. Expectedly, frostbite has been reported to affect military personnel [3] and mountaineers [4] followed by the general population [5]. Frostbite usually occurs at the exposed area where temperature is below the freezing point, i.e., -2°C (28°F). Its severity depends upon the exposure time [6]. Frostbite injury causes loss of productivity, pain, and economic burden and has potential of permanent disability [3]. The pathogenesis of frostbite is not very clear, but according to reported studies, it includes direct cold damage to tissues and injury from ice crystal formation which causes protein disruption [7], arterial vasoconstriction, thrombus formation, and ischemia [8]. The suitable treatment of frostbite is chosen depending upon its severity and duration [9]. The clinical treatments available for frostbite are anticoagulation therapy [10], vasodilators [11, 12], thrombolytic therapy, sympathectomy [9], hyperbaric oxygen [13, 14], and surgical treatment.

Currently, there are fewer specific therapies to frostbite injuries. Aloe vera is the only plant which has manifested reduction in tissue loss and has achieved a certain degree of success in the treatment of frostbite. According to WHO estimates, about three-quarters of the world’s population use herbs for different illnesses. Cuscuta reflexa Roxb. from the Cuscutaceae family, commonly known as “Akashabela,” “Amarabela,” or “Loot,” is a perennial herb. The genera Cuscuta includes 170 parasitic species [15]. This parasitic plant species is a rootless, leafless twined sprawling thin vine that grows over a host plant. It has a heterotrophic mode of nutrition due to lack of chlorophyll and hence is completely dependent on the host plant for survival [16]. The utilization of the entire plant of Custuca reflexa is linked with the treatment of different illnesses. For instance, it is devoured as a therapeutic option for cerebral pain, tingling [17], headache, skin rashes, amnesia, epilepsy, cough, and fever [18]. The aqueous ethanolic extract of Cuscuta reflexa has been studied for its constituents and found to contain alkaloids, tannins, flavonoids, and phenolic compounds [19–21]. The plant has scientifically been investigated for various pharmacological activities like anxiolytic activity [22], hair growth potential [18, 23, 24], antitumor activity [25], and antibacterial activity [26, 27]. The crude extract has also been evaluated for antiepileptic and α-glucosidase inhibition [28]. Moreover, this plant inhibits the erythrocyte damage due to hypotonicity which is anti-inflammatory effect [29]. Additionally, the plant has been quarantined for antitumor and antiproliferative activities using different animal models [25].

Despite its traditional applications in skin diseases, there is no data available in scientific literature depicting the relationship of anti-inflammatory and wound-healing property of this plant against any cold injury [17, 30]. Encouraging anti-inflammatory activities along with its effectiveness in skin disorders motivated us to evaluate its activities in frostbite.

The aim of the study is to evaluate the healing role of Cs.Cr in frostbite that may prevent tissue loss and subsequent amputation.

2. Materials and Methods

2.1. Plant Material

A whole fresh plant of Cuscuta reflexa was collected from the vicinity of Bahawalpur City (Southern Punjab, Pakistan). It was identified from an authentic botanist, and a voucher number was issued, i.e., CR-WP-05-10-006. The plant sample was preserved for future reference in the herbarium of the Faculty of Pharmacy and Alternative Medicine, the Islamia University of Bahawalpur, Pakistan. The whole plant part of Cuscuta reflexa was dried under shade to weed out for any superfluous material.

2.2. Preparation of Crude Extract

The dried plant was then coarsely powdered in a blender. Then, it was macerated with 70% aqueous methanol for three days. The macerate was passed through muslin cloth followed by filter paper. The filtrate was evaporated in a rotary evaporator (Heidolph Laborota 4000 efficient, Germany). Finally, crude extract was collected in a China dish in the form of thick viscous liquid. It was further dried in a hot air oven at 40°C. The crude extract was weighed and stored in a freezer for phytochemical and pharmacological analysis.

2.3. Chemicals

The chemicals utilized during research work were acquired from different sources. Acetylsalicylic acid (ASA) was purchased from the local market; ketamine from chemical works of Gedeon Richter Ltd., Budapest, Hungary; and xylazine from Prix Pharmaceutica, Lahore. Hair removing cream Veet was purchased from the local market. All the doses of Cs.Cr crude extract (200, 400, and 800 mg/kg) and acetylsalicylic acid (50 mg/kg) were prepared in normal saline and administered as 4 mL/kg P.O.

2.4. Experimental Animals

Wistar albino rats weighing 130-190 g were kept at control temperature (°C) in a 12 hr light and dark cycle. They were provided with standard rodent feed and water ad libitum. The study protocols were approved by the institutional committee, i.e., PREC (Pharmacy Research Ethics Committee) of the Department of Pharmacy, Faculty of Pharmacy and Alternative Medicine, the Islamia University of Bahawalpur.

2.5. Induction of Frostbite

We have followed the Chigunadze et al. model to induce frostbite [31] with minor modifications. Animals were anesthetized with ketamine and xylazine (10 : 1), and hair was removed with hair removal cream (Veet cream). It was applied for 3 minutes, and then, cream was removed with dried and wet cotton swabs, respectively. Simulated contact frostbite was produced with the help of metal weighing cm which was precooled up to -73°C in a freezer. It was then made to contact the shaved area of the rat’s skin for 3 minutes (Figure 1). After induction of injury, animals were returned to their cages for completion of the thawing process at room temperature. Standard and test drug treatment was started after 24 h.

(a)

(b)

(c)

(d)

(e)

2.6. Biochemical Assay

A blood sample was collected from the animals’ eye using nonheparinized capillary tubes. The determined parameters include platelet count, total leukocyte count, hemoglobin, WBCs, and RBCs, although only platelet count and WBCs showed significant changes.

2.7. Determination of Lipid Peroxidation

Malondialdehyde, as a marker for lipid peroxidation, was determined in serum by the double heating method of Draper and Hadley with some modifications. The principle of the method is based on spectrophotometric measurement of the color produced during the reaction of TBA with malondialdehyde. For this purpose, 2.5 mL of 100 g/L trichloroacetic acid solution was added into 0.5 mL serum in a centrifuge tube and placed in a boiling water bath for 15 min. After cooling under tap water, the supernatant was transferred into a test tube containing 1 mL of 6.7 g/L TBA solution and placed again in a boiling water bath for 15 min. The solution was then cooled under tap water, and its absorbance was measured spectrophotometrically at 532 nm. The concentration of malondialdehyde was calculated using the following equation: .

2.8. Wound Area Analysis

Photographs were taken by a digital camera on alternative days, and images were then analyzed by ImageJ software (National Institutes of Health, Bethesda, MD) [32]. The wound area was calculated as .

2.9. Analysis of Percentage Wound Area Recovered

The wound area that recovered was measured from the photographs by using ImageJ software (National Institutes of Health, Bethesda, MD). Then, the percentage of the wound area was calculated as .

2.10. Statistical Analysis

The values were expressed as the . Statistical analysis was performed with two-way ANOVA followed by Bonferroni’s test. Results were considered nonsignificant () if , significant () if , and highly significant () if . The data was compiled and statistically analyzed by using GraphPad Prism version 5.

3. Results

3.1. Cuscuta reflexa Crude Extract Decreases the Area and Percentage of Wound

The Cs.Cr remarkably reduced the wound area both dose- and time-dependently as shown in Figures 2 and 3. The frostbite-induced group showed signs of relative wound healing at the end of the study (21^st day), while similar results were obtained in the Cs.Cr (800 mg/kg)-administered group after the 7^th day sparing significant and permanent tissue losses (Figures 2 and 3).

Figure 3

Graphical representation of the frostbite wound-healing area and percentage survival area. (a) Wound area reduction in mm; (b) percentage survival area during the phase of the study. The graph shows the manifestation of values (mm) and percentages on frostbite induction on the 3^rd, 7^th, 14^th, and 21^st days. The values are expressed as the of six animals in a group. Statistical analysis is performed with two-way ANOVA followed by Bonferroni’s test. All the groups are compared with the frostbite control group. Results are nonsignificant () if , significant () if , and highly significant () if .

3.2. Effect of Crude Extract of Cuscuta reflexa on Complete Blood Count (CBC)

CBC of the experimental animals is performed on respective sampling days. Expectedly, no other parameter shows the variation except the platelet count. Platelet count increases immediately after induction of injury. This marked increase is countered by the Cs.Cr as shown in Figure 4.

3.3. Effect of Cuscuta reflexa Extract on Malondialdehyde

Flavonoids have antioxidant activity derived from plants [33]. Frostbite is virtually due to oxidative stress, and this ongoing process is generally measured by secondary products such as lipid peroxidation [34]. Malondialdehyde is a potent indicator of the lipid peroxidation level [35, 36].

The frostbite control group shows an increase in lipid peroxidation content till the 21^st day. Treatment groups and standard groups were compared with the frostbite control group. The treatment group with a dose 800 mg/kg showed a marked decrease in malondialdehyde content, i.e., 1.68 nmol/mg on the 3^rd day, and it is significant (), and there is a highly significant () decrease on the 14^th day, i.e., 1.33 nmol/mg. Cs.Cr given in doses 200, 400, and 800 mg/kg shows a dose-dependent activity as shown in Figure 5 and Table 1.

4. Discussion

Frostbite is a common occurrence in colder zones of the globe experienced by the local population, sportsmen, and tourists. It usually occurs when skin temperature drops below -0.5°C [37]. With the rise in snowstorms, avalanches, growing tourism, climate change, and increase in global sporting activities, the frostbite events are naturally on the rise. Amputation of limbs and sepsis are the major frostbite complications [38] that demand the attention of the scientific community. Our goal of the study was to search and analyze the effects of Cs.Cr on an induced frostbite model [32]. The metal bars were utilized for freezing dorsal tissue and observing wound-healing progression through granulation and reepithelialisation. This model allows quantification of the affected skin surface area, histology, healing rate, and skin loss [32]. Previously reported models are good at explaining the wound-healing process after frostbite injury, but they are complex because of radioisotopes and blood vessels overlapping [32].

Our study results show that necrosis of tissues can be induced by a frozen metal bar after it makes contact with the skin. Eschar appears after 2 to 3 days (shown in Figure 2). Visual inspection can be done, and therapy administered can give visible effects. Likewise, the treatment effects of Cs.Cr were palpable during the course of the study. Cs.Cr dose- and time-dependently reduced the area and percentage of induced frostbite wound at the dose of 200 mg/kg, 400 mg/kg, and 800 mg/kg. Positive changes in the healing process were evident even in the first seven days at the dose of 200 mg/kg of Cs.Cr, possibly preventing the early tissue loss and damage to the deeper organs. The positive changes continued till the 21^st day. This reflects the anti-inflammatory and early wound-healing properties of Cs.Cr in frostbite, which is particularly important in saving the tissue damages that usually occur within the first few hours of injury. ASA was used as a positive control drug for its well-known wound-healing and anti-inflammatory activities.

Increased concentration of malondialdehyde is an indication of lipid peroxidation [39]. Malondialdehyde is the oxidation product of fatty acids. The malondialdehyde level in rats after the exposure to cold in frostbite is due to the generation of free radicals. Our study indicates that the increased level of malondialdehyde is controlled by the administration of Cs.Cr effectively. Therefore, it can be concluded that it can scavenge free radicals and thus can reduce oxidative stress.

The phytochemical constituents that are present in medicinal plants possess medicinal and physiologic properties [40]. It was revealed that Cs.Cr was particularly rich in flavonoids, quinones, and alkaloids (Table 1). Our results are in agreement with the previous findings that suggest the anti-inflammatory [20] and wound-healing properties of flavonoids [41]. Furthermore, the phytochemical screening of Cs.Cr is already reported and connected with its wound-healing properties [42].

5. Conclusion

Conclusively, Cs.Cr is significantly effective in frostbite through the reduction of inflammation, although further studies should be performed to identify the molecular mechanism of these biological activities.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Acknowledgments

We would like to thank our entire laboratory staff at COMSATS University Islamabad, Lahore Campus, for helping at various stages of the study. The study was supported by the Department of Pharmacy, the Islamia University of Bahawalpur, and the College of Pharmacy and Health Sciences, Ajman University, Ajman, United Arab Emirates.

Supplementary Materials

Graphical abstract. (Supplementary Materials)

References

E. A. Gross and J. C. Moore, “Using thrombolytics in frostbite injury,” Journal of Emergencies, Trauma, and Shock, vol. 5, no. 3, pp. 267–271, 2012.
View at: Publisher Site | Google Scholar
I. Harirchi, A. Arvin, J. H. Vash, and V. Zafarmand, “Frostbite: incidence and predisposing factors in mountaineers,” British Journal of Sports Medicine, vol. 39, no. 12, pp. 898–901, 2005.
View at: Publisher Site | Google Scholar
J. Hu, H. Li, X. Geng et al., “Pathophysiologic determination of frostbite under high altitude environment simulation in Sprague-Dawley rats,” Wilderness & Environmental Medicine, vol. 27, no. 3, pp. 355–363, 2016.
View at: Publisher Site | Google Scholar
K. Hewitt, Glaciers in human life, in Glaciers of the Karakoram Himalaya, Springer, 2014.
View at: Publisher Site
O. Goertz, T. Hirsch, B. Buschhaus et al., “Intravital pathophysiologic comparison of frostbite and burn injury in a murine model,” Journal of Surgical Research, vol. 167, no. 2, pp. e395–e401, 2011.
View at: Publisher Site | Google Scholar
T. Gonzaga, K. Jenabzadeh, C. P. Anderson, W. J. Mohr, F. W. Endorf, and D. H. Ahrenholz, “Use of intra-arterial thrombolytic therapy for acute treatment of frostbite in 62 patients with review of thrombolytic therapy in frostbite,” Journal of Burn Care & Research, vol. 37, no. 4, pp. e323–e334, 2016.
View at: Publisher Site | Google Scholar
S. E. McIntosh, M. Opacic, L. Freer et al., “Wilderness Medical Society practice guidelines for the prevention and treatment of frostbite: 2014 update,” Wilderness & Environmental Medicine, vol. 25, no. 4, pp. S43–S54, 2014.
View at: Publisher Site | Google Scholar
K. Elfberg, Förfrysningsskador–förebyggande åtgärder och initial behandling, Goteborgs Universitet, 2014.
C. Sachs, M. Lehnhardt, A. Daigeler, and O. Goertz, “The triaging and treatment of cold-induced injuries,” Deutsches Ärzteblatt International, vol. 112, no. 44, pp. 741–747, 2015.
View at: Publisher Site | Google Scholar
R. L. McCauley, D. J. Smith, M. C. Robson, and J. P. Heggers, “Frostbite and other cold-induced injuries,” in Wilderness Medicine: Management of Wilderness and Environmental Emergencies, pp. 129–145, Mosby, St Louis, MO, 3rd edition, 1995.
View at: Google Scholar
R. L. Snider and J. M. Porter, “Treatment of experimental frostbite with intra-arterial sympathetic blocking drugs,” Surgery, vol. 77, no. 4, pp. 557–561, 1975.
View at: Google Scholar
O. Goertz, H. Haddad, L. von der Lohe et al., “Influence of ISDN, l-NAME and selenium on microcirculation, leukocyte endothelium interaction and angiogenesis after frostbite,” Burns, vol. 41, no. 1, pp. 145–152, 2015.
View at: Publisher Site | Google Scholar
T. Kemper, V. M. de Jong, H. A. Anema, A. van den Brink, and R. van Hulst, “Frostbite of both first digits of the foot treated with delayed hyperbaric oxygen: a case report and review of literature,” Undersea & Hyperbaric Medicine, vol. 41, no. 1, pp. 65–70, 2014.
View at: Google Scholar
C. Handford, P. Buxton, K. Russell et al., “Frostbite: a practical approach to hospital management,” Extreme Physiology & Medicine, vol. 3, no. 1, p. 7, 2014.
View at: Publisher Site | Google Scholar
M. Albert, B. Kaiser, S. van der Krol, and R. Kaldenhoff, “Calcium signaling during the plant-plant interaction of parasitic Cuscuta reflexa with its hosts,” Plant Signaling & Behavior, vol. 5, no. 9, pp. 1144–1146, 2010.
View at: Publisher Site | Google Scholar
B. Kaiser, G. Vogg, U. B. Fürst, and M. Albert, “Parasitic plants of the genus Cuscuta and their interaction with susceptible and resistant host plants,” Frontiers in Plant Science, vol. 6, 2015.
View at: Publisher Site | Google Scholar
N. Ahmad, S. Anwar, H. Fazal, and B. H. Abbasi, “Medicinal plants used in indigenous herapy by people of Madyan Valley in district Swat, Pakistan,” Int J Med Aromat Plants, vol. 3, no. 1, pp. 47–54, 2013.
View at: Google Scholar
S. Patel, M. K. Nag, V. Sharma, N. S. Chauhan, and V. K. Dixit, “A comparative in vivo and in vitro evaluation of hair growth potential of extracts and an isolate from petroleum ether extract of Cuscuta reflexa Roxb,” Beni-Suef University Journal of Basic and Applied Sciences, vol. 3, no. 3, pp. 165–171, 2014.
View at: Publisher Site | Google Scholar
T. Gautam, S. Gautam, S. Gautam, R. K. Keservani, and A. K. Sharma, “Phytochemical screening and wound healing potential of Cuscuta reflexa,” 中国药学 (英文版), vol. 24, no. 5, pp. 292–302, 2015.
View at: Google Scholar
H. A. Begum, M. Hamayun, K. Zaman, A. Hussain, and M. Ruaf, “Phytochemical evaluation of ethnobotanically selected medicinal plants of Mardan, Pakistan,” Journal of Advanced Botony and Zoology, vol. 3, no. 1, pp. 1–5, 2015.
View at: Google Scholar
S. Muthukkumarasamy and M. VKA, “Isolation and characterization of bioactive metabolites in Cuscuta reflexa Roxb,” Journal of Natural Sciences, vol. 1, no. 2, pp. 134–139, 2010.
View at: Google Scholar
S. Thomas, S. Shrikumar, C. Velmurugan, and B. S. A. Kum, “Evaluation of anxioltic effect of whole plant of “Cuscuta reflexa”,” World Journal of Pharmacy and Pharmaceutical Sciences (WJPPS), vol. 4, no. 4, pp. 1245–1253, 2015.
View at: Google Scholar
S. Pandit, N. S. Chauhan, and V. Dixit, “Effect of Cuscuta reflexa Roxb on androgen-induced alopecia,” Journal of Cosmetic Dermatology, vol. 7, no. 3, pp. 199–204, 2008.
View at: Publisher Site | Google Scholar
S. Patel, V. Sharma, N. S. Chauhan, M. Thakur, and V. K. Dixit, “Hair growth: focus on herbal therapeutic agent,” Current Drug Discovery Technologies, vol. 12, no. 1, pp. 21–42, 2015.
View at: Publisher Site | Google Scholar
D. Chatterjee, R. K. Sahu, A. K. Jha, and J. Dwivedi, “Evaluation of antitumor activity of Cuscuta reflexa Roxb (Cuscutaceae) against Ehrlich ascites carcinoma in Swiss albino mice,” Tropical Journal of Pharmaceutical Research, vol. 10, no. 4, 2011.
View at: Publisher Site | Google Scholar
D. Kalita and J. Saikia, “Ethonomedicinal, antibacterial and antifungal potentiality of Centella asiatica, Nerium indicum and Cuscuta reflexa-widely used in Tiwa tribe of Morigaon district of Assam, India,” International Journal of Phytomedicine, vol. 4, pp. 380–385, 2012.
View at: Google Scholar
R. Islam, M. S. Rahman, and S. M. Rahman, “GC-MS analysis and antibacterial activity of Cuscuta reflexa against bacterial pathogens,” Asian Pacific Journal of Tropical Disease, vol. 5, no. 5, pp. 399–403, 2015.
View at: Publisher Site | Google Scholar
S. K. Dokuparthi, D. N. Banerjee, A. Kumar, V. Singamaneni, A. K. Giri, and S. Mukhopadhyay, “Phytochemical investigation and evaluation of antimutagenic activity of the extract of Cuscuta reflexa Roxb by Ames test,” International Journal of Pharmaceutical Sciences and Research, vol. 5, no. 8, p. 3430, 2014.
View at: Google Scholar
P. B. Udavant, S. V. Satyanarayana, and C. D. Upasani, “Preliminary screening of Cuscuta reflexa stems for anti inflammatory and cytotoxic activity,” Asian Pacific Journal of Tropical Biomedicine, vol. 2, no. 3, pp. S1303–S1307, 2012.
View at: Publisher Site | Google Scholar
L. Sharma and S. Khandelwal, “Weeds of rajasthan and their ethno-botanical importance,” Studies on Ethno-Medicine, vol. 4, no. 2, pp. 75–79, 2017.
View at: Publisher Site | Google Scholar
A. L. Chigunadze, E. B. Artyushkova, V. N. Mishustin, G. N. Goryainova, and E. V. Artyushkova, “Experimental justification of new way of pharmacological correction for contact frostbite using dslet opioid peptide and serotonin adipinate to enhance surgycal treatment,” Research Result Pharmacology and Clinical Pharmacology, vol. 2, no. 2, pp. 3–19, 2016.
View at: Google Scholar
L. J. Auerbach, M. G. Galvez, B. K. de Clerck et al., “A novel mouse model for frostbite injury,” Wilderness & Environmental Medicine, vol. 24, no. 2, pp. 94–104, 2013.
View at: Publisher Site | Google Scholar
F. Pourmorad, S. Hosseinimehr, and N. Shahabimajd, “Antioxidant activity, phenol and flavonoid contents of some selected Iranian medicinal plants,” African Journal of Biotechnology, vol. 5, no. 11, 2006.
View at: Google Scholar
Z. A. Placer, L. L. Cushman, and B. C. Johnson, “Estimation of product of lipid peroxidation (malonyl dialdehyde) in biochemical systems,” Analytical Biochemistry, vol. 16, no. 2, pp. 359–364, 1966.
View at: Publisher Site | Google Scholar
D. Bonnes-Taourel, M.-C. Guérin, and J. Torreilles, “Is malonaldehyde a valuable indicator of lipid peroxidation?” Biochemical Pharmacology, vol. 44, no. 5, pp. 985–988, 1992.
View at: Publisher Site | Google Scholar
H. Draper, L. Polensek, M. Hadley, and L. McGirr, “Urinary malondialdehyde as an indicator of lipid peroxidation in the diet and in the tissues,” Lipids, vol. 19, no. 11, pp. 836–843, 1984.
View at: Publisher Site | Google Scholar
J. Fudge, “Preventing and managing hypothermia and frostbite injury,” Sports Health, vol. 8, no. 2, pp. 133–139, 2016.
View at: Publisher Site | Google Scholar
E. Cauchy, E. Chetaille, M. Lefevre, E. Kerelou, and B. Marsigny, “The role of bone scanning in severe frostbite of the extremities: a retrospective study of 88 cases,” European Journal of Nuclear Medicine, vol. 27, no. 5, pp. 497–502, 2000.
View at: Publisher Site | Google Scholar
M. Hamlet, J. Veghte, W. D. Bowers, and J. Boyce, “Thermographic evaluation of experimentally produced frostbite of rabbit feet,” Cryobiology, vol. 14, no. 2, pp. 197–204, 1977.
View at: Publisher Site | Google Scholar
D. Tsikas, “Assessment of lipid peroxidation by measuring malondialdehyde (MDA) and relatives in biological samples: analytical and biological challenges,” Analytical Biochemistry, vol. 524, pp. 13–30, 2017.
View at: Publisher Site | Google Scholar
B. Fernandez-Rojas and G. Gutierrez-Venegas, “Flavonoids exert multiple periodontic benefits including anti-inflammatory, periodontal ligament-supporting, and alveolar bone-preserving effects,” Life Sciences, vol. 209, pp. 435–454, 2018.
View at: Publisher Site | Google Scholar
S. Lodhi and A. K. Singhai, “Wound healing effect of flavonoid rich fraction and luteolin isolated from Martynia annua Linn. on streptozotocin induced diabetic rats,” Asian Pacific Journal of Tropical Medicine, vol. 6, no. 4, pp. 253–259, 2013.
View at: Publisher Site | Google Scholar
T. Gautam, S. P. Gautam, R. K. Keservani, and A. K. Sharma, “Phytochemical screening and wound healing potential of Cuscuta reflexa,” Journal of Chinese Pharmaceutical Sciences, vol. 5, p. 003, 2015.
View at: Google Scholar

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Copyright © 2020 Waseem Hassan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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