Suzaku Observation of the Anomalous X-ray Pulsar 1E 1841-045

We report the results of a Suzaku observation of the anomalous X-ray pulsar (AXP) 1E 1841-045 at a center of the supernova remnant Kes 73. We confirmed that the energy-dependent spectral models obtained by the previous separate observations were also satisfied over a wide energy range from 0.4 to ~70 keV, simultaneously. Here, the models below ~10 keV were a combination of blackbody (BB) and power-law (PL) functions or of two BBs wit h different temperatures at 0.6 - 7.0 keV (Morii et al. 2003), and that above ~20 keV was a PL function (Kuiper Hermsen Mendez 2004). The combination BB + PL + PL was found to best represent the phase-averaged spectrum. Phase-resolved spectroscopy indicated the existence of two emission regions, one with a thermal and the other with a non-thermal nature. The combination BB + BB + PL was also found to represent the phase-averaged spectrum well. However, we found that this model is physically unacceptable due to an excessively large area of the emission region of the blackbody. Nonetheless, we found that the temperatures and radii of the two blackbody components showed moderate correlations in the phase-resolved spectra. The fact that the same correlations have been observed between the phase-averaged spectra of various magnetars (Nakagawa et al. 2009) suggests that a self-similar function can approximate the intrinsic energy spectra of magnetars below ~10 keV.Comment: Accepted for publication in the PAS

The Arginine Residue within the C-Terminal Active Core of Bombyx mori Pheromone Biosynthesis-Activating Neuropeptide is Essential for Receptor Binding and Activation

In most lepidopteran insects, the biosynthesis of sex pheromones is regulated by pheromone biosynthesis-activating neuropeptide (PBAN). Bombyx mori PBAN (BomPBAN) consists of 33 amino acid residues and contains a C-terminus FSPRLamide motif as the active core. Among neuropeptides containing the FXPRLamide motif, the arginine (Arg, R) residue at the second position from the C-terminus is highly conserved across several neuropeptides, which can be designated as RXamide peptides. The purpose of this study was to clarify the role of the Arg residue in the BomPBAN active core. We synthesized 10-residue peptides corresponding to the C-terminal part of BomPBAN with a series of replacements at the second position from the C-terminus, termed the C2 position, and measured their efficacy in stimulating Ca2+ influx in insect cells expressing a fluorescent PBAN receptor chimera (PBANR–EGFP) using the fluorescent Ca2+ indicator, Fura Red–AM. The PBAN analogs with the C2 position replaced with alanine (Ala, A), aspartic acid (Asp, D), serine (Ser, S), or l-2-aminooctanoic acid (Aoc) decreased PBAN-like activity. RC2A (SKTRYFSPALamide) and RC2D (SKTRYFSPDLamide) had the lowest activity and could not inhibit the activity of PBAN C10 (SKTRYFSPRLamide). We also prepared Rhodamine Red-labeled peptides of the PBAN analogs and examined their ability to bind PBANR. In contrast to Rhodamine Red-PBAN C10 at 100 nM, none of the synthetic analogs exhibited PBANR binding at the same concentration. Taken together, our results demonstrate that the C2 Arg residue in BomPBAN is essential for PBANR binding and activation

Application of low-frequency electricity and stellate ganglion block therapy to inferior alveolar neuroparalysis following tooth extraction : Evaluation of facial skin temperature elevations via thermography

Mentolabial paralysis occurs as a result of inferior alveolar nerve injury consequent to tooth extraction. Stellate ganglion block (SGB) therapy, acupuncture and magnetic electrotherapy (AME) are utilized for the treatment of neuroparalysis following tooth extraction. The SGB therapy includes 30injections (2-3times/week) as a single set, and subsequently, the therapeutic effects are re-evaluated. To determine the efficacy of the treatment, patient symptoms and skin temperature increase at the site of the hypoesthesia serves as indices. Subtle temperature changes, which were detected via thermography, were converted into numeric values in this study. Treatment was conducted in collaboration with the family dentist over a 20-month period from the 5^ to the 25^ month from the onset of the hypoesthesia. The mean temperatures at the site of the hypoesthesia was compared, for an SGB-only (n=5) and an SGB/AME combination (n=5) treatment. The results found that the level of hypoesthesia, which was measured with a Semmes-Weinstein monofilament (SW) sensory tester, improved from φ3.84 to φ2.44-3.22. The temperature at the site of the hypoesthesia increased by 0.8℃ following the SGB injection ; in contrast, the temperature at the site of hypoesthesia increased by 2.5℃ following application of the SGB/AME combination. In inferior alveolar neuroparalysis arising as a consequence of tooth extraction, the surface thermo graphic temperature measurement at the site of the hypoesthesia was effective to observe the temperature increase due to SGB injection and to the SGB/AME combination ; additionally, it offers a substantiation for the treatment efficacy for the patients

Evaluation of a practical skills education method involving the determination of vital signs : consciousness, pulse, respiration, body temperature, and blood pressure

In 2003, practical skills education in vital signs (VS) was introduced to fourth-year dental students. The practical skills education consisted of an assessment of consciousness, pulse, respiration, and the determination of body temperature and blood pressure (vital signs check, VSC). The effect of the practical skills VSC education among fourth-year dental students were evaluated and the findings are discussed in this report. The subjects were two groups of fourth-year dental students ; the 2003 practical skills education group (n=94) and the 2002 group not receiving the practical skills training (n=104). The practical skills training with respect to VSC [involving a 60-minute lecture and a 20-minute video learning session, description examination, written examination (50 questions to confirm accurate base knowledge of operations), a reading (4200 characters, four figures, and five tables equivalent), demonstrations and commentary : Following the presentation of slides describing the subject matter, a qualified instructor demonstrated VSC and provided commentary to resolve student misunderstanding (10-minute session), mutual training in VSC performed with pairs of student, with 1 instructor for 2 pairs of students, second written examination : the same as the first immediately after the practical skill training, general comment and a third written examination], involved evaluation of consciousness, pulse, respiration, and the measurement of body temperature and blood pressure, offered sufficient content and appropriate educational outcomes

Re-Evaluation of the PBAN Receptor Molecule: Characterization of PBANR Variants Expressed in the Pheromone Glands of Moths

Sex pheromone production in most moths is initiated following pheromone biosynthesis activating neuropeptide receptor (PBANR) activation. PBANR was initially cloned from pheromone glands (PGs) of Helicoverpa zea and Bombyx mori. The B. mori PBANR is characterized by a relatively long C-terminus that is essential for ligand-induced internalization, whereas the H. zea PBANR has a shorter C-terminus that lacks features present in the B. mori PBANR critical for internalization. Multiple PBANRs have been reported to be concurrently expressed in the larval CNS of Heliothis virescens. In the current study, we sought to examine the prevalence of multiple PBANRs in the PGs of three moths and to ascertain their potential functional relevance. Multiple PBANR variants (As, A, B, and C) were cloned from the PGs of all species examined with PBANR-C the most highly expressed. Alternative splicing of the C-terminal coding sequence of the PBAN gene gives rise to the variants, which are distinguishable only by the length and composition of their respective C-terminal tails. Transient expression of fluorescent PBANR chimeras in insect cells revealed that PBANR-B and PBANR-C localized exclusively to the cell surface while PBANR-As and PBANR-A exhibited varying degrees of cytosolic localization. Similarly, only the PBANR-B and PBANR-C variants underwent ligand-induced internalization. Taken together, our results suggest that PBANR-C is the principal receptor molecule involved in PBAN signaling regardless of moth species. The high GC content of the C-terminal coding sequence in the B and C variants, which makes amplification using conventional polymerases difficult, likely accounts for previous “preferential” amplification of PBANR-A like receptors from other species

Establishment of Sf9 Transformants Constitutively Expressing PBAN Receptor Variants: Application to Functional Evaluation

To facilitate further evaluation of pheromone biosynthesis activating neuropeptide receptor (PBANR) functionality and regulation, we generated cultured insect cell lines constitutively expressing green fluorescent protein chimeras of the recently identified Bombyx mori PBANR (BommoPBANR) and Pseudaletia separata PBANR (PsesePBANR) variants. Fluorescent chimeras included the BommoPBANR-A, -B, and -C variants and the PsesePBANR-B and -C variants. Cell lines expressing non-chimeric BommoPBANR-B and -C variants were also generated. Functional evaluation of these transformed cell lines using confocal laser microscopy revealed that a Rhodamine Red-labeled PBAN derivative (RR-C10PBANR2K) specifically co-localized with all of the respective PBANR variants at the plasma membrane. Near complete internalization of the fluorescent RR-C10PBANR2K ligand 30 min after binding was observed in all cell lines except those expressing the BommoPBANR-A variant, in which the ligand/receptor complex remained at the plasma membrane. Fluorescent Ca2+ imaging further showed that the BommoPBANR-A cell line exhibited drastically different Ca2+ mobilization kinetics at a number of RR-C10PBANR2K concentrations including 10 μM. These observations demonstrate a clear functional difference between the BommoPBANR-A variant and the BommoPBANR-B and -C variants in terms of receptor regulation and activation of downstream effector molecules. We also found that, contrary to previous reports, ligand-induced internalization of BommoPBANR-B and BommoPBANR-C in cell lines stably expressing these variants occurred in the absence of extracellular Ca2+