CC BY-NC-ND 4.0 · Eur J Dent 2021; 15(04): 741-745
DOI: 10.1055/s-0041-1729677
Original Article

In vivo Hemostatic Activity of Jatropha mollissima: A Triple-Blinded, Randomized, Controlled Trial in an Animal Model

Maria Vitoria Oliveira Dantas
1   Federal University of Campina Grande, Patos, Paraíba, Brazil
,
Paula Lima Nogueira
1   Federal University of Campina Grande, Patos, Paraíba, Brazil
,
Filipe de Oliveira Lima
1   Federal University of Campina Grande, Patos, Paraíba, Brazil
,
Denis Candeia Pereira Oliveira
1   Federal University of Campina Grande, Patos, Paraíba, Brazil
,
Emanuelly Nara Severiano Gomes
1   Federal University of Campina Grande, Patos, Paraíba, Brazil
,
José Filipe Bacalhau Rodrigues
2   Academic Unit of Materials Engineering, Federal University of Campina Grande, Campina Grande, Paraíba, Brazil
,
Solomon Kweku Sagoe Amoah
2   Academic Unit of Materials Engineering, Federal University of Campina Grande, Campina Grande, Paraíba, Brazil
,
Rosana Araújo Rosendo
3   Academic Unit of Biological Sciences - Dentistry, Federal University of Campina Grande, Patos, Paraíba, Brazil
,
Elizandra Silva da Penha
3   Academic Unit of Biological Sciences - Dentistry, Federal University of Campina Grande, Patos, Paraíba, Brazil
,
Antonio Flávio Medeiros Dantas
4   Academic Unit of Veterinary Medicine, Federal University of Campina Grande, Patos, Paraíba, Brazil
,
Marcus Vinícius Lia Fook
2   Academic Unit of Materials Engineering, Federal University of Campina Grande, Campina Grande, Paraíba, Brazil
,
5   Department of Orthodontics, Faculty of Dentistry, Federal University of Juiz de Fora, Governador Valadares, Minas Gerais, Brazil
,
Luanna Abílio Diniz Melquiades de Medeiros
3   Academic Unit of Biological Sciences - Dentistry, Federal University of Campina Grande, Patos, Paraíba, Brazil
› Author Affiliations

Abstract

Objective The objective of this study was to evaluate the hemostatic activity of the sap from Jatropha mollissima (Pohl) Baill. in rats.

Materials and Methods Twenty-four Wistar rats were randomized into four groups (n = 6): the JM25 and JM40 groups were treated with ethanolic extract from the sap of J. mollissima, in a concentration of 25 and 40 mg·mL1, respectively; the MO group was treated with Monsel’s solution and the control group SC with a 0.9% sodium chloride solution.

Statistical Analysis Data were submitted to the Kurskal–Wallis’ test, followed by Dunn’s post hoc (p < 0.05).

Results There was a significant reduction in the bleeding time of the group from the JM25 extract (p = 0.001) when compared with MO and SC. There were no statistically significant differences between groups JM25 and JM40 (p > 0.05). The JM25 group did not present rebleeding, a result significantly different from the MO group (p = 0.001). Monsel’s solution showed significant bleeding, six times greater than the control group SC.

Conclusion The J. mollissima extract, in the concentration of 25 mg·mL1, showed the highest hemostatic efficiency and was found to be a promising biomaterial for the elaboration of a hemostatic product.



Publication History

Article published online:
24 August 2021

© 2021. European Journal of Dentistry. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India

 
  • References

  • 1 Panwar V, Sharma A, Thomas J. et al. In-vitro and in-vivo evaluation of biocompatible and biodegradable calcium-modified carboxymethyl starch as a topical hemostat. Materialia (Oxf) 2019; 7: 100373
  • 2 Wiegand C, Abel M, Hipler UC. et al Hemostatic wound dressings: predicting their effects by in vitro tests. J Biomater Appl 2019; 33 (09) 1285-1297
  • 3 Rosi F, Perale G, Masi M. Introduction: chemical engineering and medicine. In: Controlled Drug Delivery Systems. Springer Nature, Switzerland; 2016, 1 Edition: 1–7
  • 4 Barbosa HM, Albino AM, Cavalcante FS, Lima RA. Phychochemical approach of secondary metabolites in Sola num acanthodes (SOLANACEAE) HOOK. South Am J Basic Educ Tech 2017; 4 (01) 30-41
  • 5 Bruning MC, Mosegui GB, Vianna CM. [The use of phytotherapy and medicinal plants in primary healthcare units in the cities of Cascavel and Foz do Iguaçu - Paraná: the viewpoint of health professionals]. Cien Saude Colet 2012; 17 (10) 2675-2685
  • 6 Silva NC, Vitor A, Bessa HH, Barros RM. Use of medicinal plants and herbal medicines for health. Única Cadernos Acadêmicos 2017; 3 (01) 10-14
  • 7 Dias WLF, Junior EPV, Oliveira MDDA. et al. Cytogenotoxic effect, phytochemical screening and antioxidant potential of Jatropha mollissima (Pohl) Baill leaves. S Afr J Bot 2019; 123: 30-35
  • 8 Soares AFB, Silva JN. Study and monitoring of the generation of technologies using gender plants Jatropha. Cadernos de Prospecção 2018; 12 (02) 413
  • 9 Trindade MJS, Lameira OA. Species from the Euphorbiaceae family used for medicinal purposes in Brazil. Rev Cuba Plantas Med 2014; 19 (04) 292-309
  • 10 Sun L, Li M, Ma C, Li P. Preparation and evaluation of Jatropha curcas based catalyst and functionalized blend components for low sulfur diesel fuel. Fuel 2017; 206: 27-33
  • 11 Braquehais ID, Vasconcelos FR, Ribeiro ARC, et al. Toxicological, antibacterial, and phytochemical preliminary study of the ethanolic extract of Jatropha mollissima (Pohl) Baill (pinhão-bravo, Euphorbiaceae) leaves, collected in Tauá, Ceará, Northeastern Brazil. Rev Bras Plantas Med 2016;18(2:Suppl 1):582–587
  • 12 Souza DD, Cavalcanti NB. Biometry of fruits and seeds of Jatropha mollissima (Pohl) Baill. (Euphorbiaceae). Acta Biol Catarinense 2019; 6 (02) 115-122
  • 13 Neto RFQ, Júnior HNA, Freitas CIA. et al. The Jatropha mollissima (Pohl) Baill: chemical and pharmacological activities of the latex and its extracts. Semin Cienc Agrar 2020; 40 (06) 2613-2624
  • 14 Pimentel LA, Riet-Correa B, Dantas AF, Medeiros RM, Riet-Correa F. Poisoning by Jatropha ribifolia in goats. Toxicon 2012; 59 (05) 587-591
  • 15 Penha ESD, Lacerda-Santos R, Carvalho MGF, Oliveira PT. Effect of Chenopodium ambrosioides on the healing process of the in vivo bone tissue. Microsc Res Tech 2017; 80 (11) 1167-1173
  • 16 Penha ESD, Lacerda-Santos R, de Medeiros LADM. et al Effect of chitosan and Dysphania ambrosioides on the bone regeneration process: a randomized controlled trial in an animal model. Microsc Res Tech 2020; 83 (10) 1208-1216
  • 17 Lacerda-Santos R, de IH Meneses, Sampaio GA, Pithon MM, Alves PM. Effect of degree of conversion on in vivo biocompatibility of flowable resin used for bioprotection of mini-implants. Angle Orthod 2016; 86 (01) 157-163
  • 18 Meneses IHC, Sampaio GAM, Carvalho FG. et al In vivo biocompatibility, mechanical, and antibacterial properties of cements modified with propolis in different concentrations. Eur J Dent 2020; 14 (01) 77-84
  • 19 Mesquita JA, Lacerda-Santos R, Sampaio GAM, Godoy GP, Nonaka CFW, Alves PM. Evaluation in vivo of biocompatibility of differents resin-modified cements for bonding orthodontic bands. An Acad Bras Cienc 2017; 89 (03) (Suppl) 2433-2443
  • 20 Lacerda-Santos R, Roberto BMS, de Siqueira Nunes B, Carvalho FG, Dos Santos A, Dantas AFM. Histological analysis of biocompatibility of different surgical adhesives in subcutaneous tissue. Microsc Res Tech 2019; 82 (07) 1184-1190
  • 21 Lacerda-Santos R, Lima ABL, Penha ESD. et al In vivo biocompatibility of silicon dioxide nanofilm used as antimicrobial agent on acrylic surface. An Acad Bras Cienc 2020; 92 (01) e20181120
  • 22 Sampaio GM, de Meneses IH, de Carvalho FG. et al Antimicrobial, mechanical and biocompatibility analysis of chlorhexidine digluconate-modified cements. J Clin Exp Dent 2020; 12 (02) e178-e186
  • 23 Lacerda-Santos R, Sampaio GA, Moura MdeF. et al Effect of different concentrations of chlorhexidine in glass-ionomer cements on in vivo biocompatibility. J Adhes Dent 2016; 18 (04) 325-330
  • 24 Leary S, Underwood W, Anthony R, et al. AVMA guidelines for the euthanasia of animals, 2020 edition, Schaumburg: American Veterinary Medical Association, 2020:1-121
  • 25 Sampaio GAM, Lacerda-Santos R, Cavalcanti YW, Vieira GHA, Nonaka CFW, Alves PM. Biocompatibility of ionomeric cements modified by red propolis: a morphological and immunohistochemical analysis. J Adhes Dent 2020; 22 (05) 515-522
  • 26 Cavalcante NB, Diego da Conceição Santos A, Guedes da Silva Almeida JR. The genus Jatropha (Euphorbiaceae): a review on secondary chemical metabolites and biological aspects. Chem Biol Interact 2020; 318 (01) 108976
  • 27 Badgujar SB. Evaluation of hemostatic activity of latex from three Euphorbiaceae species. J Ethnopharmacol 2014; 151 (01) 733-739
  • 28 Uday P, Achar RR, Bhat RP. et al. Laticiferous plant proteases in wound care. Int J Pharm Pharm Sci 2015; 7 (Suppl. 01) 44-49
  • 29 Khoshmohabat H, Paydar S, Kazemi HM, Dalfardi B. Overview of agents used for emergency hemostasis. Trauma Mon 2016; 21 (01) e26023
  • 30 Apu AS, Ireen K, Bhuyan SH, Matin M, Hossain MF, Rizwan F.. Evaluation of analgesic, neuropharmacological and anti-diarrheal potential of Jatropha gossypifolia (Linn.) leaves in mice. J Med Sci 2012; 12 (08) 274-279
  • 31 Oduola T, Adeosun GO, Oduola TA, Avwioro GO, Oyeniyi MA. Mechanism of action of Jatropha gossypifolia stem latex as a haemostatic agent. Eur J Gen Med 2005; 2 (04) 140-143
  • 32 Ebrahimi F, Mahmoudi J, Torbati M, Karimi P, Valizadeh H. Hemostatic activity of aqueous extract of Myrtus communis L. leaf in topical formulation: in vivo and in vitro evaluations. J Ethnopharmacol 2020; 249 (01) 112398
  • 33 Pereira B, Brazón J, Rincón M, Vonasek E. Browplasminin, a condensed tannin with anti-plasmin activity isolated from an aqueous extract of Brownea grandiceps Jacq. flowers. J Ethnopharmacol 2017; 198 (01) 282-290
  • 34 Martelli A, Andrade TAM, Santos GMT. Perspectives in the use of herbal medicines in tissue healing: systematic review. Arch Health Invest 2018; 7 (08) 344-350
  • 35 Soltani R, Haghighat A, Fanaei M, Asghari G. Evaluation of the effect of green tea extract on the prevention of gingival bleeding after posterior mandibular teeth extraction: a randomized controlled trial. Evid Based Complement Alternat Med 2014; 2014: 857651
  • 36 Byun J-Y, Lee S, Lee JI, Yoon H-Y. Comparison of hemostatic efficacy and cytotoxicity of three ferric subsulfate-and chitosan-based styptics in different formulations using a rat tail bleeding model. Korean J Vet Res 2018; 58 (03) 119-124
  • 37 Tompeck AJ, Gajdhar AUR, Dowling M. et al A comprehensive review of topical hemostatic agents: the good, the bad, and the novel. J Trauma Acute Care Surg 2020; 88 (01) e1-e21
  • 38 Abzaeva KA, Zelenkov LE. Modern topical hemostatic agents and unique representatives of their new generation. Russ Chem Bull 2015; 64: 1233-1239
  • 39 Amer MZ, Mourad SI, Salem AS, Abdelfadil E. Correlation between international normalized ratio values and sufficiency of two different local hemostatic measures in anticoagulated patients. Eur J Dent 2014; 8 (04) 475-480