Home About us Contact
|
Home About us Contact | ||
|
|
||
Several Different Species (several + different_species)
Selected AbstractsDifferent methods of monitoring susceptibility of oilseed rape beetles to insecticidesEPPO BULLETIN, Issue 1 2008T. Thieme The resistance of oilseed rape pollen beetles to lambda-cyhalothrin has increased in Germany over the period 2002 to 2007. Oilseed rape pollen beetles are very good at dispersing, therefore field results should always be compared with those of laboratory experiments. The response of oilseed rape pollen beetles to active substances may not be the same as that to formulated products. Bioassays in which beetles are exposed to insecticides on either complete inflorescences or flower buds give different results. It is evident that samples of the genus Meligethes collected in the field can include several different species. Monitoring for insecticide resistance should be done using only the true oilseed rape pollen beetle. [source] Sex differences in songbirds 25 years later: What have we learned and where do we go?MICROSCOPY RESEARCH AND TECHNIQUE, Issue 6 2001Gregory F. Ball Abstract About 25 years ago, Nottebohm and Arnold reported that there are profound male-biased sex differences in volume in selected nuclei in telencephalic portions of the song control system. This review focuses on issues related to the cellular bases of these sex differences in volume and comparative studies that might elucidate the function of this variation between the sexes. Studies utilizing a variety of neurohistological methods in several different species to define the boundaries of two key telencephalic song nuclei HVc and the robust nucleus of the archistriatum (RA) all tend to find a sex difference in volume in agreement with Nissl-defined boundaries. Sex differences in volume in nuclei such as HVc and RA are associated with differences in cell size and cell number. Other attributes of the phenotype of cells in these nuclei are also different in males and females such as the number of cells expressing androgen receptors. Comparative studies have been employed to understand the function of these sex differences in the brain. In some songbird species, females sing rarely or not at all, and the brain nuclei that control song are many times larger volume in males than females. In other species, males and females sing approximately equally, and the brain nuclei that control song are approximately equal between the sexes. Recently, statistical methods have been employed to control for phylogenetic effects while comparing the co-evolution of traits. This analysis indicates that the evolution of sex differences in song has co-evolved with the evolution of sex differences in singing behavior in songbird species. Future studies should focus on the function of the smaller song control nuclei of females and investigate the role these nuclei might play in perception as well as in production. Microsc. Res. Tech. 54:327,334, 2001. © 2001 Wiley-Liss, Inc. [source] Innervation of the Pelvic Limb of the Adult Ostrich (Struthio camelus)ANATOMIA, HISTOLOGIA, EMBRYOLOGIA, Issue 5 2010T. El-Mahdy With 24 figures Summary The pelvic limb of the ostrich is innervated by the lumbar and sacral plexuses. The lumbar plexus gave rise to several nerves (N.s) including, N. coxalis cranialis, lateral and cranial femoral cutaneous N.s, N. femoralis, cranial, caudal and medial crural cutaneous N.s, and N. obturatorius. The remaining nerves emanated from the sacral plexus. The N. iliotibial, N. ischiofemoralis, N. iliofibularis, and N. coxae caudalis were distributed in the thigh, while the N. ischiadica, which terminated as the tibial and fibular N.s that innervated the leg and foot. The tibial N. gave rise to the parafibular N. then divided to form the Nn. suralis medialis and lateralis. The N. suralis medialis continued as the N. metatarsalis plantaris medialis. The parafibular N. continued as the N. plantaris lateralis, which terminated as the R. digitalis of the fourth digit. The fibular N. terminated as the superficial and deep fibular N.s. The superficial fibular N. continued as the N. metatarsalis dorsalis lateralis and divided into two digital N.s to the third and fourth digits. The deep fibular N. crossed the ankle joint and continued as the N. metatarsalis dorsalis medialis that continued as the R. digitalis of the third digit. In general, the innervation of the pelvic limb of the ostrich was similar to the pelvic limbs of several different species of domesticated birds, including the chicken. We discuss the few differences as well as appropriate sites to perform nerve blocks for the lateral and medial dorsal and the lateral plantar N.s. [source] Enzymatic stability of 2,-ethylcarbonate-linked paclitaxel in serum and conversion to paclitaxel by rabbit liver carboxylesterase for use in prodrug/enzyme therapyBIOPHARMACEUTICS AND DRUG DISPOSITION, Issue 5 2008Tadatoshi Tanino Abstract In prodrug/enzyme therapy for cancer, information on the sensitivity of hydrolytic enzymes to prodrug is required to reduce adverse effects of the parental drug and to find the activating enzyme. The aim of this study was to characterize the enzymatic stability of 2,-ethylcarbonate-linked paclitaxel (TAX-2,-Et) in the sera of several different species including humans. TAX-2,-Et disposition in serum was kinetically analysed using models with hydrolytic and/or degradation processes. To further evaluate the capability of liver carboxylesterases (CESs) in TAX-2,-Et hydrolysis, a CES isolated from rabbit liver (Ra-CES) was utilized as a model enzyme. Rat serum provided rapid enzymatic hydrolysis of TAX-2,-Et with a half-life of 4 min. The degradation of paclitaxel (TAX) (degradation rate constant, 0.16,h,1) was accompanied by the formation of an unknown compound. The conversion to TAX was almost completely inhibited by phenylmethyl sulfonylfluoride (PMSF) and bis(p-nitrophenyl) phosphate (BNPP). In human and rabbit sera, the degradation rate constant of TAX-2,-Et was 5.1,×,10,2 and 0.15,h,1, respectively, when excepting hydrolysis. The degradation products had the same molecular weight as TAX-2,-Et. The amount of TAX produced accounted for only 8,11% of the decrease in TAX-2,-Et after a 9 h exposure to rabbit or human serum. PMSF, but not BNPP, inhibited more than 90% of the TAX production in a 1.5,h incubation with human or rabbit serum. Ra-CES enzyme converted TAX-2,-Et to TAX with Vmax and Km of 74.7±13.8 nmol/min/mg protein and 8.8±2.8 µM, respectively. These results indicate that TAX-2,-Et is sensitive to serum CESs, but not cholinesterases. However, serum CESs show species-dependent hydrolysis of TAX-2,-Et. Although human serum allows the slow release of TAX, TAX-2,-Et is expected to reduce the side-effects of TAX. The Ra-CES enzyme is capable of hydrolysing TAX-2,-Et, which may be beneficial for the development of a TAX-2,-Et/enzyme therapy strategy for ovarian cancer. Copyright © 2008 John Wiley & Sons, Ltd. [source] | |||||||||||||