S R Naik’s research while affiliated with Federal University of Paraíba and other places

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Publications (22)


Effect of piperine bioavailability of oxyphenylbutazone in rats
  • Article

February 1999

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51 Reads

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35 Citations

INDIAN DRUGS

A.M. Majumdar

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J.N. Dhuley

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V.K. Deshmukh

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S.R. Naik

Piperine, an alkaloid isolated from Piper nigrum Linn. was studied for its effect on bioavailability of oxyphenylbutazone in rats. Piperine enhanced the bioavailability of oxyphenylbutazone and thereby potentiated its anti- inflammatory activity. The enhanced bioavailability was found to be the net result of increased absorption of oxyphenylbutazone from gastro-intestinal tract and inhibition of liver microsomal drug metabolising enzyme(s).


Protection by Rhinax in various models of ulceration in rats

January 1999

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12 Reads

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16 Citations

Journal of Ethnopharmacology

The effect of Rhinax on gastric damage in different animal models including gastric ulceration induced by a necrotic agent such as 0.6 N HCl, indomethacin, and intragastric distension was studied. Treatment with Rhinax at a dose of 160 mg/kg protected gastric mucosa against the damage induced by oral administration of indomethacin and intragastric distension. The volume and acidity of gastric juice in pyloric ligated rats was reduced by Rhinax. It also significantly promoted gastric mucus secretion in normal animals. On the basis of these observations, we conclude that Rhinax possesses anti-ulcer activity and that the observed activity may be due to the modulation of defensive factors by improvement in gastric cytoprotection.


Effect of Rhinax on bacterial lipopolysaccharide induced endotoxemia in rats

April 1998

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6 Reads

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9 Citations

Indian Journal of Experimental Biology

Administration of lipopolysaccharide (LPS) at 3 mg/kg, i.p. in rats resulted in reduced food intake, febrile hyperthermia, decreased body weight and reduced muscle performance in treadmill tests. It also induced some biochemical changes like increased serum levels of transaminases, acid phosphatase, pseudocholinesterase, free fatty acids and decreased blood glucose and liver glycogen levels. Rhinax (RHX), a herbal formulation, at 160 mg/kg, p.o. improved muscle performance but had no effect on the elevated temperature or the reduced body weight of rats weakened by LPS. It also normalised various biochemical alterations induced by LPS. The results of these studies indicate efficacy of RHX as an antifatigue agent to improve muscular performance.


Protective effect of Rinax, a herbal formulation, against CCl4-induced liver injury and survival in rats

May 1997

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32 Reads

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69 Citations

Journal of Ethnopharmacology

Rhinax, a herbal formulation, was investigated for its protective activity against CCl4-induced liver injury and survival in rats. Oral administration of Rhinax at a dose of 80 mg/kg significantly reduces the hepatotoxic effects of CCl4. It also significantly improves the survival of rats at a dose of 160 mg/kg. On the basis of these observations, we conclude that Rhinax possesses anti-hepatotoxic activity and that the observed activity may be due to the increased activity of cytochrome P450, thereby exerting an inhibitory effect on reductive pathways of CCl4.


Acute toxicity of Aureofungin to fresh water fish Gumbussia affinis

January 1997

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20 Reads

Pestology

Static bioassay tests were conducted using technical grade Aureofungin to study its toxicity during different seasons to Gumbussia affinis from the fresh water pond of Pune University. Acute toxicity studies for 96 h showed that Gumbussia is sensitive to Aureofungin in summer at times of high temperature, pH and total carbonate contents of the water used, than in the monsoon and winter. LC0 and LC50 values were determined for Gumbussia affinis during summer, monsoon and winter. Statistical analyses showed that Gumbussia affinis was more sensitive to Aureofungin during summer (p 0.001) than in monsoon and winter. Behavioural changes and mortality of the fishes were dose-related. The results are discussed in the light of possible effects of Aureofungin on this fresh water fish.


Effect of 6-MFA, an interferon inducer obtained from fungus Aspergillus ochraceus on hepatic mixed function oxidase system in rats

November 1996

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7 Reads

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4 Citations

Indian Journal of Experimental Biology

Effect of 6-MFA (sixth mycelial fraction of acetone), an interferon inducer obtained from fungus A. ochraceus on hepatic mixed function oxidase system (MFO) of rat has been investigated. Treatment with 6-MFA, 100 mg/kg/day, ip for 1-5 days to adult rats inhibited significantly the different indices of MFO system, viz. hepatic cytochrome P-450, cytochrome b5 content, cytochrome c reductase, aminopyrine-N-demethylase and acetanilide hydroxylase activities. Similar treatment for 3 days in young growing rats significantly inhibited MFO system's components except acetanilide hydroxylase activity which showed marked elevation. These effects seem to be specific as in vitro experiments suggested that 6-MFA does not compete with subsdtrates nor it acts as a sponge reacting with the end product to give false inhibitory effect. It is concluded from the present study that 6-MFA like other interferon inducers depresses MFO system in rats. Its possible clinical implications are discussed.


Toxicological profile of aureofungin: a potent plant antifungal antibiotic

December 1995

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37 Reads

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5 Citations

Indian Journal of Experimental Biology

J N Dhuley

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P H Raman

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[...]

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S R Naik

Aureofungin is a heptaene type of antifungal antibiotic used for controlling plant fungal infections and diseases, during pre and post harvesting period of various crops. Acute and subacute oral toxicity of aureofungin in rats was studied along with haematological, urine analysis and other biochemical parameters related to liver and kidney organ functions. The results of these studies indicate mild toxic symptoms at higher doses which were reversible following its withdrawal.



Inhibition of lipid peroxidation by piperine during experimental inflammation in rats

June 1993

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27 Reads

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61 Citations

Indian Journal of Experimental Biology

Carrageenin induced rat paw oedema shows a direct co-relationship with liver lipid peroxidation and not with kidney or brain. Pretreatment with piperine or oxyphenylbutazone reduced the liver lipid peroxidation, acid phosphatase and oedema induced by carrageenin. However, no such co-relationship was observed with treatment of these anti-inflammatory agents in control animals. It is, therefore, suggested that the inhibition of these liver enzymes is non specific in nature.



Citations (13)


... Antidepressant, hepatoprotective, antioxidant, anticancer, antibacterial and antispasmodic properties are all present in piperine's fruit (2). Additionally, piperine has the power to lower inflammation, relieve pain, enhance digestion, and boost bioavailability (3). Additionally, piperine is capable of improving bioavailability, increasing digestion and reducing discomfort (4). ...

Reference:

Corrosion Inhibition of carbon steel XC70 in two acidic media (0.1 N H 2 SO 4 ( and (0.1 N HCl) by weight loss method using Black Pepper Extract as corrosion inhibitor
Effect of piperine bioavailability of oxyphenylbutazone in rats
  • Citing Article
  • February 1999

INDIAN DRUGS

... Furthermore, peptaibols seem to cause pathological changes to the ultrastructure of mitochondria (Reed and Lardy, 1975;Bruckner and Toniolo, 2013). It has been shown that the peptaibol AAM exhibits trypanocidal activity in a mouse model for trypanosomiasis (Kumar et al., 1991), effect attributed to the channel-forming capacity that dissipates the parasite mitochondrial membrane potential, or alters the parasite's plasma membrane integrity (Nagaraj et al., 2001). ...

Evaluation of microbial metabolites for trypanocidal activity: Significance of biochemical and biological parameters in the mouse model of trypanosomiasis
  • Citing Article
  • March 1991

Japanese Journal of Medical Science and Biology

... Terpenes are bioactive compounds that occur both as hydrocarbons and terpenoids (oxygen-containing compounds), present naturally in many herbs, and are known to possess significant hypoglycaemic properties [20]. Terpenes show antidiabetic potential by either of the mechanisms that include stimulation of insulin secretion [21][22][23][24], enhanced plasma BER (β-endorphin immunoreactivity) by activation of α1-ARs to improve the discharge of β-endorphin, which has the potential to excite opioid micro-receptors to diminish gluconeogenesis in the liver and boost glucose uptake in the soleus muscle [25,26], α-glucosidase inhibition [27][28][29], increasing glucose uptake and glycogen synthesis and blood insulin concentrations. It appears that the reason for this outcome was the facilitation of insulin secretagogue impact in β-cells of the pancreas [30] by appreciably augmenting the blood pyruvate concentration and liver glycogen level [31] by improving insulin discharge from β-cells of the pancreas, which is due to improved stimulation of β-cells and insulin synthesis [32][33][34], and by enhancing glucose utilization in striated muscles, which leads to lower plasma glucose levels and increases in insulin discharge from pancreatic β-cells [24,28,35,36]. ...

Probable mechanism of hypoglycemic activity of basic acid, a natural product isolated from. Bumelia sartorum
  • Citing Article
  • May 1991

Journal of Ethnopharmacology

... Some studies have reported that pepper had a high antibacterial ability (75% antibacterial activity) to fight infections in the respiratory tract and oral cavity, had helped improve mood, and had battled depression, reducing stress and fatigue due to substances that had caused the body to increase serotonin production 5 . Piperine, found in black pepper, has the chemical formula C 17 H 19 NO 3 , belonging to the alkaloid, characterized by its mild alkaline nature and yellow crystalline structure, showing strong solubility in ethanol and chloroform. ...

Anti-inflammatory activity of pepper
  • Citing Article
  • July 1990

Japanese Journal of Medical Science and Biology

... The fruits include Central Nervous System (CNS) depressants, antipyretic, analgesic, hepatoprotective, bioavailability enhancers [16][17] , antioxidant 18 and antiinflammatory activities. Piplartin, Piperlogumine, Piperidine, Starch, Resin and pungent alkaloids are all found in the fruits of P.nigrum and P.longum. ...

Effect of piperine on pentobarbitone induced hypnosis in rats
  • Citing Article
  • June 1990

Indian Journal of Experimental Biology

... Decreased serum Cp levels have been positively correlated with a decrease in dopamine transporter density in patients with Parkinson [63]. Cp acts as a defense mechanism against inflammation [64]. Neurodevelopmental disorders such as ASD are closely related with neuroinflammation [65]. ...

Role of ceruloplasmin in inflammation: Increased serum ceruloplasmin levels during inflammatory conditions and its possible relationship with anti-inflammatory agents
  • Citing Article
  • August 1985

Pharmacological Research Communications

... (family: Sapotaceae) is a large and tall tree commonly known as 'Quixaba', 'Quixabeira', 'Tranceporteira', 'Sacutiaba' and 'Rompe-gibao' in northeastern Brazil. It naturally grows from north of Minas Gerias to Piaui (41). An unsaturated triterpene acid named bassic acid, isolated from the ethanol extract of root bark of B. surtorum exhibited significant hypoglycemic activity in alloxan induced diabetic rat models. ...

Chemistry and pharmacology of an ethanol extract of Bumelia sartorum
  • Citing Article
  • November 1985

Journal of Ethnopharmacology

... The pancreas of 4 groups of alloxan diabetic rats treated with MCE (150 mg/kg and 300 mg/kg), glibenclamide (4 mg/kg) and 1% CMC (10 ml/kg) respectively, for a period of 30 days and one group of normal control rats were isolated and preserved in 10%(v/v) formalin. Histopathological evaluation of the tissues [14] was carried out at clinico-pathology laboratory, Haffkine Institute, Mumbai, India. The histological effects were transformed into numerical scoring system and finally expressed in terms of mean ± SEM Evaluation of hypolipidemic activity of MCE in old obese rats A group of 24 old obese male albino Wistar rats [14] were divided into 3 groups of 8 animals each. ...

Hypolipidemic-hypocholesterolemic activity of JA-20, a new polyene macrolide
  • Citing Article
  • February 1981

Hindustan Antibiotics Bulletin

... This result may be attributed to BP's reduction of acetyl-CoA production, which is required for fat metabolism. Studies on animals have demonstrated that the bioactive components of BP, especially piperine, have antiperoxidative effects (Dhuley et al., 1993). Because of this, broiler hens' diets supplemented with BP caused lower levels of plasma cholesterol and LDL cholesterol (Galib et al., 2011;Ghaedi et al., 2014;Shahverdi et al., 2013;Puvaca et al., 2014), which could be attributed to BP antioxidative properties. ...

Inhibition of lipid peroxidation by piperine during experimental inflammation in rats
  • Citing Article
  • June 1993

Indian Journal of Experimental Biology

... Of critical importance for successful use of polyene macrolide antibiotics (PMAs) for nonmedical application such as lucensomycin [28], tetramycin [29], aureofungin [30,31], etc. as highly effective fungicides is not only a broad spectrum of antifungal action but also fast and easy degradation to nontoxic compounds after use. This suggests eco-friendliness and expedience of the practical application of perimycin. ...

Toxicological profile of aureofungin: a potent plant antifungal antibiotic
  • Citing Article
  • December 1995

Indian Journal of Experimental Biology