Caffeine may be enhancing the tumoricidal effect of anticancer drugs, resp. DNA—damaging agents and possibly may aid in overcoming natural drug resistance [1] . An ionizing radiation and alkylating agents to potentiate the cytotoxic effects of caf on DNA damage agents [2] . Shoyab [3] proposed that the antitumorigenic effect of caffeine may be related to its ability to inhibit the bonding of active metabolites of carcinogens to cellular DNA. Traganos et al. [4] potentiate the cytotoxicity of a variety of DNA damaging agents presumable by reducing the ability of the cells to repair potentially lethal lesions and may pay a more general role to protecting cells against planar aromatic molecules such as intercalating agents. Therefore caffeine may be considered in designing strategies to modulate the activity of the intercalating drugs in vivo, e.g. in lowering drug toxicity when inadvertently applied at too bright doses [5] . The combination of caffeine with adriamycin can significantly increase the in vivo antitumor activity of this agent without increasing its side effect [6] . The effect of caffeine on adriamycin concentration in the cell plays an important role in the mechanism by which caffeine enhances adriamycin antitumor activity [7] . Also acts as a biochemical modulator of adriamycin [8] . The combination of adriamycin, cis- Pt(NH₃)₂Cl₂, and caffeine shoved partial response, and caffeine did not increase the vide effect of anticancer drugs [9] . Caffeine reduced the inhibitory effect of pirarubicin on the incorporation of thymine into DNA and uridine into RNA in cells [10] . Inhibit post replication repair of both UV and chemically induced damage in DNA lesions caused by cis-Pt(NH₃)₂Cl₂ [11] . Induction of DNA fragmentation during G2+M phase by caffeine modulates the cytotoxicity of cis-Pt(NH₃)₂Cl₂ in human osteosarcomic cells (strain) and the antitumor effect of cis-paltinum on transplanted osteosarcoma in athymic since [12] [13] . Caffeine enhanced the antitumor activity of doxorubicin with increasing doxorubicin concentration in tumors in vivo [14]. Caffeine is an inhibitor of DNA repair [15] . Caffeine inhibited the carcinogenic action of cigarette smoke condensate fraction before application [16] . The concomitant consumption of caffeine and cigarette constitutes a higher risk for the developing fetus [17] . Caffeine also potentiates the activity of cyclophosphamide [18] . Caffeine decreased the paracetamol induced hepatic toxicity [19] [20] . Caffeine significantly potentiates the therapeutic potential of acetaminophenol in man [21] . Anderson et al. [22] found that caffeine increases plasma epinephrine, cold increases oxygen consumption and carbohydrate metabolism, while decreasing lipid metabolism, Nishiyama et al. [23] found that caffeine also induced enhanced lipid oxidation as show by the significantly lower respiratory gas exchange ratio and increases in diastolic blood pressure during exercise. The results showed that caffeinated beverages have a potential to be useful supplements to the prescription of exercise for individuals who experience a depressed activity of the autonomic nervous system. Caffeine affects the central nervous system to binding to adenosine receptors, and it has acute and chronic dose dependent, effects on brain fraction [24] . Caffeine also showed the rate of compensatory sleep after sleep deprivation, as indexed by the duration of sleep states and sleep continuity [25] . Caffeine also alters cardiovascular dynamics by augmenting arterial blood pressure [26] . The secretary effect of caffeine may be mainly due to mobilization of calcium from an intracellular calcium pool [27] . High caffeine intake may predispose to cortical bone loss from the proximal femur [28] . Kawaga et al. [29] found, that caffeine facilitates the conversion of allopurinol to oxopurinol and produces high plasma level of oxopurinol in man. Valdes et al. [30] found that when caffeine intake during the gestational and lactation period by their

Scheme 1. Structure of purine alkaloids.

dams and the growing period of pups affect the maxillary components of their offspring. The stimulating action of caffeine depends on the level and source of arousal [31] .

Biological activity of theophyline also covers wide variety and will be shortly resented. Ito et al. [32] found that the low dose of theophyline exerts an anti-asthma effect through increasing activation of HDAC which is subsequently recruited by corticosteroids to suppress inflammatory genes. Sagara et al. [33] also confirmed that top has anti-inflammatory activity which is pertinent to the treatment of bronchial asthma, when is added to bronchodilator actions. Top decreases the natural sputum eosinophyl chemolactic activity present in asthmatic [34] . Taheuchi et al. [35] found that top is able to induce apoptosis of the IL-3-activated eosinoplies in patient with bronchial asthma, and that its clinical effectiveness may be due to the reduction of inflammatory cells in the airway. Small dose of top inhibited platelet-activating factor receptor mRNA expression in asthma blood lymphatic cells [36] . Changquan et al. [37] used top as therapeutic agent for the treatment of asthma. Pediatric asthma can be treatment by top even at low concentration [37] . Top suppresses that production of proinflammatory cytokines via inhibitor of NF-κB activation through protection of the IB protein [38] . Top treatment caused a significant increase in renal and muscle carnitine palmitoyltransferase activity [39] [40] . Top also enhanced mobilization of lipid from adipose tissues, which consequently stimulated an increased carnitine transport into the kidney tissues to from fatty acyl-carnitine groups for subsequent oxidation inside the mitochondria [41] . Oral top administration (100 mg/kg/day) changes the levels of carnitine in plasma and tissues and increases the activity of carnitine acetyltransferase in the cardiac tissues of rats [42] .

Mandal and Poddar found [43] that top under no tolerant condition produced region specific inhibition of adenylate cyclase activity and hence central adenosynergic activity which may be a resultant effect of heterogeneous distribution of extra cellular adenosine receptor (A1 and A2) of different brain regions and also the availability of adenosine for interaction to the intracellular receptor sites (P-site) under this condition. Development of tolerance to top may reduce the brain regional adenylate cyclase activity by increasing the A1 receptor population and hence may stimulate the central adenosynergic activity. Effects of xantine derivatives on phosphatydylcholine secretion in rat were studied by Omura et al. [44] . Top increased the PC secretion the Co-culture of type II pneumocytes and activated eosinophils through the inhibition of phosphodiesterases of the antagonism of adenosine reduced AMP stimulation and facilitated glucose inhibition [45] . Long term top treatment may potentiate or suppress the immune response, depending on the dose, through the tissue (liver/spleen/thymus) specific modulation of adenosine deaminase activity and plasma corticosterone status [46] . Top therapy at optimal doses my not exert adverse side effects on bone homeostasis, but patients receiving supratherapeutic doses of top should be under close exams, in order to periodic future bone mass status [47] Heparin and top in the medium are effective in activating metabolic enzymes, maintaining longer sperm mobility, and efficiently inducing hyper activated sperm even of the sperm of asthenozoospermia [48]

Top increased serum glucocorticoid levels in a dose-dependent manner [49] top used as a muscle relaxant or vasodilator [50] . Top is also effective as a diuretic and cardiac stimulant [51] . Top has a high ulcer score, increase the development of dental caries and this effect may be related to organism, alternation of salivary components [52] .

Tob inhibited adriamycin efflux in vitro, increased the antitumor activity of adriamycin and the concentration of adriamycin in tumors [8] . Tob increased the concentration of adriamycin in the tumor without any effects on that in the heart and the liver [53] . Tob inhibited the doxorubicin efflux from tumor cells, increased the doxorubicin concentration in a tumor, and enhanced the antitumor effect of doxorubicin [54] . Tob greatly suppressed urethane-induced tumorigenesis and teratogenesis, whereas top did not [55] . Tob as well as top produced high antiinflammatory activity against acute inflamation induced by acetic acid while caf showed no significant effect [56] . Tob and caf differentiated normally developing somniferous cords made up of Sertoli and germ cells, soon followed by the differentiation of functionally active Leyding cells appearing in the newly formed interstitum [57] . The ratio of tob/caf has effect on hepatic human flavin monooxygenase 3 activity [58] . Tob significantly increased the mouse’s ambulatory activity [59] .