PriMera Scientific Medicine and Public Health (ISSN: 2833-5627)

Review Article

Volume 2 Issue 3

Sanay Leaves Treatment in Constipation Rats Restores Defence System in Red Blood Cells

Trilok Kumar and BL Gupta*

March 01, 2023

DOI : 10.56831/PSMPH-02-046

Abstract

     The defensive enzymes like glutathione preoxidase, glutathione reductase and catalase along with the defensive metabolites like reduced glutathione and oxidised glutathione were measured in red blood cells of acute constipated rats also along with sanay treated constipated rats. It was observed a decrease in GPx activity in both sexes of rats i.e., males and females. The GR activity in constipated rats was shown to be increased by more than GPx activity. The catalase activity has been observed to be increased insignificantly in acute condition. However, the GSH levels were found to be decreased in acute constipated rats but GSSG levels enhanced in acute condition. The sanay leaves treatment to acute condition rats restored the changed enzymes activities and metabolites levels.

     The liver function test carried out by the two enzymes namely GOT & GPT which increased in constipated rats. It shows that the enhanced GOT & GPT activities caused dysfunction of liver and invite kinds of liver diseases. The creatinine levels in red blood cells showed insignificant changes in both acute constipated rats and its treated condition with sanay leaves. It may be concluded that sanay treatment restores the low defense system found in constipated rats as well as the liver function which is slightly changed during constipation.

References

  1. Andreoli SP, Mallett and Bergstein JM. “Role of glutathione in protecting endothelial cells against hydrogen peroxide oxidant injury”. J. Lab. Clin. Med 108 (1986): 190-198.
  2. Artur Y., et al. “Age-related variations of enzymatic defenses against free radicals and peroxides”. EXS 62 (1992): 359-367.
  3. Blankenberg S., et al. “Glutathione peroxidase 1 activity and cardiovascular events in patients with coronary artery disease”. N Engl J Med 349 (2003): 1605-1613.
  4. Burton GJ and Jauniaux E. “Placental oxidative stress: from miscarriage to preeclampsia”. J. Soc. Gynaecol. Invest 11 (2010): 342-352.
  5. Bergmeyer HU and Bernt E. Glutamate-oxaloacetate transaminase in Method of enzymatic analysis (ed) H U Bergmeyer (New York Academic Press) (1974): 727-733.
  6. Beutler E, West C and Blume KGJ. “The removal of leucocytes and platelets from whole blood”. Lab Cin Med 88 (1976): 328-333.
  7. Beutler E. Method in Hematology (Beautler, E. Ed. Longman, U.K 16 (1986): 52-72.
  8. Cohen G and Hochstein P. “Glutathione peroxidase: the primary agent for the elimination of hydrogen peroxide in erythrocytes”. Biochemistry 2 (1963): 1420-1428.
  9. Combs GF Jr. “Status of selenium in prostate cancer prevention”. Br J Cancer 91 (2004): 195-199.
  10. Copeland PR and Driscoll DM. “Purification, redox sensitivity, and RNA binding properties of SECIS-binding protein 2, a protein involved in selenoprotein biosynthesis”. J Biol Chem 274 (1999): 25447-25454.
  11. Deponte M. “Glutathione catalysis and the reaction mechanisms of glutathione dependent enzymes”. Biochemica et Biophysica Acta 1830 (2013): 3217-3266.
  12. Erden M and Bor NM. “Change of reduced glutathione, glutathione reductase, and glutathione preoxidase after radiation in guinea pigs”. Biochm Med 31.2 (1984): 217-27.
  13. Gleason DM., et al. “Removal of hypernephroma and inferior vena cava: right artical tumor thrombus”. Arch Surg 105.5 (1972): 795-7.
  14. Griffith OW. “Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine”. Anal Biochem 107 (1980): 207-212.
  15. Gupta BL and Baquer NZ. “Hexokinase, G-6PDH and antioxidant enzymes in diabetic reticulocytes: Role of insulin and vanadate”. Biochem. Mol. Biol. Int 48 (1998): 1145-1152.
  16. Gupta BL, Preet A and Baquer NZ. “Protective effects of sodium orthovanadate in diabetic reticulocytes and ageing red blood cells of Wistar rats”. J Biosci 29 (2004): 73-79.
  17. Hughes S, Higgs NB and Turnberg LA. “Loperamide has antisecretory activity in the human jejunum in vivo”. Gut 25 (1984): 931-935.
  18. Johanson JF, Sonnenberg A and Koch TR. “Clinical epidemiology of chronic constipation”. J Clin Gastroenterol 11.5 (1989): 525-536.
  19. McCrea GL., et al. “A review of the literature on gender and age differences in the prevalence and characteristics of constipation in North America”. J Pain Symptom Manage 37.4 (2009): 737-745.
  20. Mullineaux P and Creissen GP. “Glutathione reductase: regulation and role in oxidative stress Oxidative stress and the molecular biology of antioxidant defenses”. Cold Spring Harbor Laboratory Press (1997).
  21. Rao SS. Constipation: evaluation and treatment of colonic and anorectal motility disorders. Gastroenterol Clin North Am 36.3 (2007): 687-711.
  22. Seybold U., et al. “Senna-induced hepatitis in a poor metabolizer”. Ann Intern Med 141 (2004): 650-651.
  23. Siegers CP and Younes M. “Clinical significance of the glutathione-conjugating system”. Pharmacol Res Commun 15.1 (1983): 1-13.
  24. Spiller HA., et al. “Skin breakdown and blisters from Senna-containing laxatives in young children”. Ann Pharmacother 37 (2003): 636-639.
  25. Talley N J., et al. “Risk factors for chronic constipation based on a general practice sample”. Am J Gastroenterol 98.5 (2003): 1107-1111.
  26. Trevisan M., et al. “Correlates of markers of oxidative status in the general population”. Am J Epidemiol 154 (2001): 348-356.
  27. Upadhayay A., et al. “Sennoside contents in Senna (Cassia angustifolis Vahl.) as influenced by date of leaf picking, packaging material and storage period”. J Stored Prod Postharv Res 2 (2011): 97-103.
  28. Wald A, Hinds JP and Caruana BJ. “Psychological and physiological characteristics of patients with severe idiopathic constipation”. Gastroenterology 97.4 (1989): 932-937.
  29. Yamada E., et al. “Clinical factors associated with the symptoms of constipation in patients with diabetes mellitus: a multicenter study”. J Gastroenterol Hepatol 33 (2017): 863-868.
  30. Yu BP and Chung HY. “Adaptive mechanisms to oxidative stress during aging”. Mech Ageing Dev 127 (2006): 436-443.
  31. Younes M and Siegers CP. “Interrelation between lipid peroxidation and other hepatotoxic events”. Biochem. Pharmacol 33 (1984): 2001-2003.