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DOI: 10.3923/pjbs.2011.954.955
URL: https://scialert.net/abstract/?doi=pjbs.2011.954.955
Any kind of metabolic abnormality in insulin pathway causes health problems, which makes the body highly vulnerable to other disease like diabetes, dyslipidemia, hypertension and liver disorders (Marchesini et al., 2003; Lim and Kim, 2008; Pervez, 2000). This altogether with hepatitis B-C infection, aggressively increases the risk of liver failure and mortality. Liver is involved in anabolic/catabolic reactions of several proteins, lipids, blood cells and toxic compounds, thus any problematic effects on it will cause heavy burden on human health. As it is the 3rd leading disease, causing mortality in Minnesota, USA; impaired fasting glucose and cirrhosis increase the death rate of liver patients (Adams et al., 2005). Liver disorders are usually linked with an increase in its enzyme concentration (Harris, 2005). For example in diabetes 2 patients, diseased liver has elevated levels of serum aminotransferases, Alanine aminotransferase (ALT), Alkaline Phosphatase (AP) and Aspartate aminotransferase (AST) etc. The increase in these enzyme levels is a major cause for end stage liver disease and patients death (Ekstedt et al., 2006). Hence, metabolic problems severely affect liver, which needs great attention and plants can efficiently behave as hepatoprotectants (Garba et al., 2006), which is likely to be due to their phytochemical composition. Ocimum gratissimum is medicinally important plant; it has large variety of phytochemicals and possesses analgesic effects (Okiemy-Andissa et al., 2004; Vieira et al., 2001). It is used in folk medicines and its analgesic effective concentrations, when used in combination with other herbs do not cause any toxicity in mice body (Iroanya et al., 2010). Moreover, it is also responsible for anti-inflammatory effects in mice. The methanolic extracts of its leaves have anti-ulcer activity and are able to protect the rats stomach from ethanol and indomethacin-induced ulcers (Akah et al., 2007). Its extract has concentration dependant relaxation effect on the rabbit jejunum and does not cause any sign of acute toxicity. Its methanolic extract is rich with flavonoids, tannins, saponins, steroids, alkaloid etc., which are responsible for its gastroprotective effects. Thus it is a rich source of phytochemicals and may also be helpful in the treatment of liver diseases.
Many practitioners consider O. gratissimu leaves as a good remedial source and Uhegbu et al. (2012) studied its claimed analgesic and hepatoprotective activities. For analgesic studies, a concentration dependant effect of its methanolic extracts was examined on mice when subjected to thermal-induced pain. These extracts delayed the time of pain perception from 3.2±0.25 sec (pretreatment reading) to 11.56±0.15 sec (after treatment reading for extracts maximum concentration used). All other (100 and 200 mg kg-1) concentration were also effective and their effects were non-significantly different from the maximum (300 mg kg-1) concentration and standard drug: acetylsalicylic acid. Thus O. gratissimum extracts was effective in lowering the pain at all concentrations. Its extract also showed distinctive hepatoprotection against CCl4 caused liver toxicity. The CCl4 implementation damaged livers veins and cells architecture; it also caused necrosis in many liver cells mainly due to increase in fat and some degrading enzymes. But the application of O. gratissimums methanolic extract conserved the liver cells and tissues from its adverse damage, as its application maintained the cells-veins arrangement and their physiology as well. Thus O. gratissimum protected the anatomical structure of liver from cytotoxication. However this was not all, its extract also protected the liver from the extensive increase in catabolic enzymes level, which were AST, ALT and ALP. The increase in enzymes level damaged the liver tissue and the application of plants methanolic extract lowered their level. Highest remedial effect was on ALP enzyme level, as the extract lowered its level from 55.4±0.27 to 30.2±0.01, while its value in healthy group was 26.2±1.32. The extracts effect on other enzymes (AST and ALT) was also significant and their levels were non-significantly different from healthy control group. Thus it can be said that enzyme level lowering activity of O. gratissimum extracts, made it an important hepatorpotective agent. As the determination of enzyme levels are important to estimate the livers health (Somchit et al., 2005; Satyapal et al., 2008). Moreover its use as analgesic agent would also help in lowering the demands of acetylsalicylic acid, because the use of acetylsalicylic acid could severely damage liver (Bjornsson and Olsson, 2005). Acetylsalicylic acid was also responsible for ecotoxicity (Cleuvers, 2004) and its reduction would protect environment. Thus, O. gratissimums analgesic and hepatoprotective property would help in saving the lives from acetylsalicylic acid caused toxicity.
So, it can be said that O. gratissimum is medicinally important plant; it has analgesic, gastroprotective and anti-inflammatory effects. Moreover the therapeutically effective concentration of its extracts does not cause acute toxicity or death of tested animal, thus its use may be safe for humans also. According to Uhegbu et al. (2012), its methanolic extracts were excellent hepatoprotectant and its analgesic property was comparable to that of acetylsalicylic acid (a potential cytotoxic pain killer). Thus its use will favor the human health more than acetylsalicylic acid; hence there should be more research on its possible cytotoxic levels and effective phytochemicals. This will guide the medicinal chemists for developing safer painkiller or hepatoprotective drug.
REFERENCES
- Uhegbu, F.O., I. Elekwa, E.I. Akubugwo, G.C. Chinyere and E.E.J. Iweala, 2012. Analgesic and hepatoprotective activity of methanolic leaf extract of Ocimum gratissimum (L.). Res. J. Med. Plant, 6: 108-115.
CrossRefDirect Link - Satyapal, U.S., V.J. Kadam and R. Ghosh, 2008. Hepatoprotective activity of livobond a polyherbal formulation against CCl4 induced hepatotoxicity in rats. Int. J. Pharmacol., 4: 472-476.
CrossRefDirect Link - Somchit, M.N., A. Zuraini, A.A. Bustamam, N. Somchit, M.R. Sulaiman and R. Noratunlina, 2005. Protective activity of turmeric (Curcuma longa) in paracetamol-induced hepatotoxicity in rats. Int. J. Pharmacol., 1: 252-256.
CrossRefDirect Link - Bjornsson, E. and R. Olsson, 2005. Outcome and prognostic markers in severe drug-induced liver disease. Hepatology, 42: 481-489.
PubMedDirect Link - Cleuvers, M., 2004. Mixture toxicity of the anti-inflammatory drugs diclofenac, ibuprofen, naproxen and acetylsalicylic acid. Ecotoxicol. Environ. Saf., 59: 309-315.
CrossRefPubMedDirect Link - Marchesini, G., E. Bugianesi, G. Forlani, F. Cerrelli and M. Lenz et al., 2003. Non-alcoholic fatty liver, steatohepatitis and the metabolic syndrome. Hepatology, 37: 917-923.
PubMed - Lim, Y.S. and W.R. Kim, 2008. The global impact of hepatic fibrosis and end-stage liver disease. Clin. Liver Dis., 12: 733-746.
CrossRefPubMedDirect Link - Adams, L.A., J.F. Lymp, J.St. Sauver, S.O. Sanderson, K.D. Lindor, A. Feldstein and P. Angulo, 2005. The natural history of nonalcoholic fatty liver disease: A population-based cohort study. Gastroenterology, 129: 113-121.
PubMedDirect Link - Pervez, K., 2000. Diagnosis and genotyping of hepatitis C virus by polymerase chain reaction in chronic liver disease patients. Pak. J. Biol. Sci., 3: 1098-1099.
CrossRefDirect Link - Harris, E.H., 2005. Elevated liver function tests in type 2 diabetes. Clin. Diabetes, 23: 115-119.
CrossRefDirect Link - Ekstedt, M., L.E. Franzen, U.L. Mathiesen, L. Thorelius, M. Holmqvist, G. Bodemar and S. Kechagias, 2006. Long-term follow-up of patients with NAFLD and elevated liver enzymes. Hepatology, 44: 865-873.
PubMed - Garba, S.H., S. Ahmadu and I.A. John, 2006. The effect of aqueous stem bark extract of Sclerocarya birrea (Hoechst) on alcohol carbon tetrachloride induced liver damage in rats. Pak. J. Biol. Sci., 9: 2283-2287.
CrossRefDirect Link - Vieira, R.F., R.J. Grayer, A. Paton and J.E. Simon, 2001. Genetic diversity of Ocimum gratissimum L. based on volatile oil constituents, flavonoids and RAPD markers. Biochem. Syst. Ecol., 29: 287-304.
PubMedDirect Link - Okiemy-Andissa, N., M.L. Miguel, A.W. Etou, J.M. Ouamba, M. Gbeassor and A.A. Abena, 2004. Analgesic effect of aqueous and hydroalcoholic extracts of three congolese medicinal plants: Hyptis suavolens, Nauclea latifolia and Ocimum gratissimum. Pak. J. Biol. Sci., 7: 1613-1615.
CrossRefDirect Link - Iroanya, O., J. Okpuzor and H. Mbagwu, 2010. Anti-nociceptive and anti-phlogistic actions of a polyherbal decoction. Int. J. Pharmacol., 6: 31-36.
CrossRefDirect Link - Akah, P.A., L. John-Africa and C.S. Nworu, 2007. Gastro-protective properties of the leaf extracts of Ocimum gratissimum L. against experimental ulcers in rat. Int. J. Pharmacol., 3: 461-467.
CrossRefDirect Link