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Research Articles

Pennisetum glaucum Protein Extract Protects RBC, Liver, Kidney, Small Intestine from Oxidative Damage and Exhibits Anticoagulant, Antiplatelet Activity

, , , , , , , , , & show all
Pages 211-223 | Received 19 Sep 2020, Accepted 12 Dec 2020, Published online: 09 Dec 2022
 

Abstract

Objective

High level of exogenous ROS in the circulation affects RBC membrane integrity which facilitates the generation of endogenous RBC ROS, implicated in series of physiological changes primarily associated with thrombosis and vital tissue damage. Although, Pennisetum glaucum (pearl millet) stores abundance of proteins, their therapeutic potential is least explored. Thus, the purpose of this study is to examine the role of Pennisetum Glaucum Protein Extract (PGE) on oxidative stress induced cell/tissue damage and thrombosis.

Method

In this investigation, protein characterization was done by using SDS-PAGE, Native-PAGE, PAS-staining and HPLC. In-vitro oxidative stress was induced in RBC using sodium nitrite. While, in-vivo oxidative stress was induced in experimental rats using diclofenac. Stress markers and biochemical parameters were evaluated. Role of PGE on thrombosis was assessed by using, in-vitro plasma recalcification time, activated partial thromboplastin time, prothrombin time, mouse tail bleeding time (In-vivo) and platelet aggregation.

Results:

PGE revealed varied range of molecular weight proteins on SDS-PAGE. PGE normalized the sodium nitrite induced oxidative damage of RBC and diclofenac induced oxidative damage in liver, kidney and small intestine. PGE exhibited anticoagulant effect by increasing the coagulation time of both PRP and PPP and mouse tail bleeding time. Furthermore, PGE prolonged the clotting time of only APTT but did not affect PT. PGE inhibited agonists ADP and epinephrine induced platelet aggregation.

Conclusion

Our findings suggest, PGE could be a better contender in the management of oxidative stress and its associated diseases.

Abbreviations

PGE=

Pennisetum Glaucum protein Extract

APPT=

Activated Partial Thromboplastin Time

PT=

Prothrombin Time

ROS=

Reactive Oxygen Species

PRP=

Platelet Rich Plasma

PPP=

Platelet Poor Plasma

SDS-PAGE=

Sodium Dodecyl Sulfate-Polyacrylamide Gel Electrophoresis

PAS=

Periodic Acid-schiff Staining

OD=

Optical Density

INR=

International Normalized Ratio

PBS=

Phosphate Buffered Saline

SOD=

Superoxide Dismutase

TCA=

Trichloro Acetatic Acid

DTNB=

Di-Thio-bis-NitroBenzoic acid

SGOT=

Serum Glutamate Oxaloacetate Transaminase

SGPT=

Serum Glutamate Pyruvate Transaminase

ALP=

Alkaline Phosphatase

DFC=

Diclofenac

Syl=

Silymarin

MED=

Minimum Edema Dose

MHD=

Minimum Hemorrhagic Dose

Author contributions

AS and DS together planned and designed the research work. CS, SMH, JK, SKMN, and CR assisted AS in the laboratory work. SSM, TTG, RR, and MS reviewed the article.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This work was supported by Vision Group of Science and Technology, Government of Karnataka, Bangalore, India for financial assistance.

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