Pharmacology and Toxicology of Proteins
نویسنده
چکیده
One of the most promising and practical applications resulting from the enormous advances made in the understanding of molecular structure and biology of proteins is in the area of therapeutics and drug development. While recombinantly produced protein and peptide drugs offer the possibility for extremely specific and potent pharmaceuticals for the modulation of biological responses, the toxicology of only a few of these novel agents has been rigorously studied. This collection of papers from a recent UCLA symposium sponsored jointly by Cetus Corporation is devoted primarily to a discussion of the unique problems now being encountered in the analysis of the pharmacokinetics, metabolism, immunogenicity, and toxicology of proteins and peptides. Specifically, the clinical pharmacology of monoclonal antibodies, interleukin-2, interferons, protease inhibitors, and thrombolytics are examined, as well as novel drug delivery systems particularly suited to these experimental therapies. Unfortunately, this volume, like so many of these hastily edited collections, is a disparate, incohesive, and largely superficial group of descriptive papers. While there are a few valuable contributions, such as the thorough review of monoclonal antibody therapies for infectious diseases, this book suffers most notably from the lack of papers devoted to toxicological testing of gene products (attributed by one speaker to the concurrent Society of Toxicology Meeting!). The clinical pharmacology of proteins and peptides represents a fascinating and largely uncharted subject, which will undoubtedly gather increased attention from both the medical and scientific communities as new drugs near clinical trials. This volume, however, serves as neither a balanced review nor an appropriate introduction to this subject. Industrial toxicologists may find their colleagues' discussions interesting and somewhat valuable, but the student or clinician interested in protein therapeutics is advised to continue reading the primary literature for now.
منابع مشابه
Screening and identification of SUMP-proteins in sub-acute treatment with diazinon
Objective(s):Small ubiquitin-like modifiers (SUMOs) are a family of ubiquitin-related, proteins that are involved in a wide variety of signaling pathways. SUMOylation, as a vital post translational modification, regulate protein function in manycellular processes. Diazinon (DZN), an organophosphate insecticide, causses oxidative stress and subsequently programmed cell death in different tissues...
متن کاملPharmacokinetics, dosage regimen and in vitro plasma protein binding of intramuscular levofloxacin in buffalo calves
The pharmacokinetics of levofloxacin following its single intramuscular administration (3 mg/kg) was investigated in six male buffalo calves. Peak plasma level of 2.95 ± 0.13μg/ml was observed at 1 h and the drug level above MIC90 in plasma was detected up to 12 h of administration. The bioavailability was 68.1 ± 5.4% and levofloxacin was bound to the plasma proteins to the extent of 19.1 ± 1....
متن کاملCyclooxygenase inhibitors combined with deuterium-enriched water augment cytotoxicity in A549 lung cancer cell line via activation of apoptosis and MAPK pathways
Objective(s): Combination chemotherapy is a rational strategy to increase patient response and tolerability and to decrease adverse effects and drug resistance. Recently, the use of non-steroidal anti-inflammatory drugs (NSAIDs) has been reported to be associated with reduction in occurrence of a variety of cancers including lung cancer. On the other hand, growing evidences suggest that deuteri...
متن کاملRecognition and characterization of Erythropoietin binding-proteins in the brain of mice
Objective(s): Erythropoietin (EPO), is a 34KDa glycoprotein hormone, which belongs to type 1 cytokine superfamily. EPO involves in erythrocyte maturation through inhibition of apoptosis in erythroid cells. Besides its main function, protective effects of EPO in heart and brain tissues have been reported. EPO has a critical role in development, growth, and homeostasis of brain. Furthermore EPO h...
متن کاملThe neuroprotective effect of lithium in cannabinoid dependence is mediated through modulation of cyclic AMP, ERK1/2 and GSK-3β phosphorylation in cerebellar granular neurons of rat
Lithium (Li), a glycogen synthase kinase-3β (GSK-3β) inhibitor, has used to attenuate thecannabinoid-induced dependence/withdrawal signs, but molecular mechanisms related to this areunclear. Recent studies indicate the involvement of upstream extracellular signal kinase1/2 (ERK1/2)and downstream GSK-3β pathways in the development of cannabinoid-induced dependence. Thisis mediated through cannab...
متن کاملThe neuroprotective effect of lithium in cannabinoid dependence is mediated through modulation of cyclic AMP, ERK1/2 and GSK-3β phosphorylation in cerebellar granular neurons of rat
Lithium (Li), a glycogen synthase kinase-3β (GSK-3β) inhibitor, has used to attenuate thecannabinoid-induced dependence/withdrawal signs, but molecular mechanisms related to this areunclear. Recent studies indicate the involvement of upstream extracellular signal kinase1/2 (ERK1/2)and downstream GSK-3β pathways in the development of cannabinoid-induced dependence. Thisis mediated through cannab...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Yale Journal of Biology and Medicine
دوره 61 شماره
صفحات -
تاریخ انتشار 1988