Relationship between Muscle Flexibility and Characteristics of Muscle Contraction in Healthy Women during Different Menstrual Phases

Objective: Skeletal muscle function is vital for preventing injury during exercise. It has been reported that skeletal muscle function fluctuates with the menstrual cycle and is considered one of the causes of injury. This study aimed to clarify the relationship between muscle flexibility and muscle contraction characteristics and their changes with the menstrual cycle. Methods: The subjects were healthy women who voluntarily participated in the study through recruitment posters. Muscle flexibility was measured with the passive knee extension (PKE) test, isokinetic knee flexor strength, and the maximum muscle strength exertion angle under two conditions of 60°/s and 120°/s in dominant hamstrings. Additionally, their correlations were analyzed and compared between the menstrual and ovulatory phases. Results: Sixteen subjects (mean age: 20.56 ± 0.73 years; body mass index: 20.21 ± 1.60) participated in the study. Correlation analysis showed a significant negative correlation between PKE and the maximum muscle strength exertion angle under the condition of 60°/s during the menstrual phase (r = –0.54; p = 0.03). No significant difference was observed in the two-group comparison of the variables measured during the menstrual and ovulatory phases. Conclusion: This study confirmed that the more flexible muscles generate the maximum strength at a more contracted position during the menstrual phase in women. In the future, it is necessary to examine the relationship between the results of this study and exercise performance and injury occurrence.     

Reflection functors for quiver varieties and Weyl group actions

We introduce reflectionfunctors on quiver varieties. They are hyper-Kähler isometries between quiver varieties with different parameters, related by elements in the Weyl group. The definition is motivated by the origial reflection functor given by Bernstein-Gelfand-Ponomarev [1], but they behave much nicely. They are isomorphisms and satisfy the Weyl group relations. As an application, we define Weyl group representations of homology groups of quiver varieties. They are analogues of Slodowys construction of Springer representations of the Weyl group. Mathematics Subject Classification (2000):Primary 53C26; Secondary 14D21, 16G20, 20F55, 33D80Supported by the Grant-in-aid for Scientific Research (No.11740011), the Ministry of Education, Japan.     

Asymmetric total synthesis of optically active α-curcumene

(R)-(?)-α-Curcumene has been prepared in 66% optical yield and in 34% overall yield in five steps by means of asymmetric Grignard cross-coupling reaction catalyzed by a nickel complex of chiral (aminoalkylferrocenyl)phosphine as a key carbon-carbon bond forming step.     

Rigidity of the Álvarez class

Let ${(M,\mathcal{F})}$ be a closed manifold with a Riemannian foliation. The Álvarez class of ${(M,\mathcal{F})}$ is a cohomology class of M of degree 1 whose triviality characterizes the minimizability or the geometrically tautness of ${(M,\mathcal{F})}$ . We show that the integral of the Álvarez class of ${(M,\mathcal{F})}$ along every closed path is the logarithm of an algebraic integer if π₁ M is polycyclic or ${\mathcal{F}}$ is of polynomial growth.     

High‐Pressure Synthesis of A2NiO2Ag2Se2 (A=Sr,Ba) with a High‐Spin Ni2+ in Square‐Planar Coordination

Square‐planar coordinate Ni²⁺ ions in oxides are exclusively limited to a low‐spin state (S=0) owing to extensive crystal field splitting. Layered oxychalcogenides A₂Ni^IIO₂Ag₂Se₂ (A=Sr, Ba) with the S=1 NiO₂ square lattice are now reported. The structural analysis revealed that the Ni²⁺ ion is under‐bonded by a significant tensile strain from neighboring Ag₂Se₂ layers, leading to the reduction in crystal field splitting. Ba₂NiO₂Ag₂Se₂ exhibits a G‐type spin order at 130 K, indicating fairly strong in‐plane interactions. The high‐pressure synthesis employed here possibly assists the expansion of NiO₂ square lattice by taking the advantage of the difference in compressibility in oxide and selenide layers.     

In vitro and in vivo evaluation of microparticulate drug delivery systems composed of macromolecular prodrugs

Macromolecular prodrugs are very useful systems for achieving controlled drug release and drug targeting. In particular, various macromolecule-antitumor drug conjugates enhance the effectiveness and improve the toxic side effects. Also, polymeric micro- and nanoparticles have been actively examined and their in vivo behaviors elucidated, and it has been realized that their particle characteristics are very useful to control drug behavior. Recently, researches based on the combination of the concepts of macromolecular prodrugs and micro- or nanoparticles have been reported, although they are limited. Macromolecular prodrugs enable drugs to be released at a certain controlled release rate based on the features of the macromolecule-drug linkage. Micro- and nanoparticles can control in vivo behavior based on their size, surface charge and surface structure. These merits are expected for systems produced by the combination of each concept. In this review, several micro- or nanoparticles composed of macromolecule-drug conjugates are described for their preparation, in vitro properties and/or in vivo behavior.     

A highly efficient hybrid method for calculating the hydration free energy of a protein

We develop a new method for calculating the hydration free energy (HFE) of a protein with any net charge. The polar part of the energetic component in the HFE is expressed as a linear combination of four geometric measures (GMs) of the protein structure and the generalized Born (GB) energy plus a constant. The other constituents in the HFE are expressed as linear combinations of the four GMs. The coefficients (including the constant) in the linear combinations are determined using the three‐dimensional reference interaction site model (3D‐RISM) theory applied to sufficiently many protein structures. Once the coefficients are determined, the HFE and its constituents of any other protein structure are obtained simply by calculating the four GMs and GB energy. Our method and the 3D‐RISM theory give perfectly correlated results. Nevertheless, the computation time required in our method is over four orders of magnitude shorter.     

Photoresponsive change of oxygen-binding affinity of a cobalt schiff-base complex with an axially coordinating stilbazole residue of a copolymer

The reversible binding reaction of oxygen to N,N'-ethylene bis(salicylideneiminato) cobalt(II) (CoS), to which a photoisomerizable stilbazole residue of copolymer 1 coordinated, was investigated. The E form of the stilbazole residues coordinating to CoS, (E)-1-CoS, showed photoisomerization into the Z form, (Z)-1-CoS, on direct ultraviolet irradiation and negligible reverse isomerization. The oxygen-binding equilibrium constant (K) values for (E)-1-CoS and (Z)-1-CoS in toluene were 3.3 x 10(-2) mmHg-1 and 4.8 x 10(-3) mmHg(-1), respectively, at 10 degrees C. Although the pK(a) values of the E and Z forms of the stilbazole residue were similar, the oxygen-binding affinity of (Z)-1-CoS was small in terms of the linear correlation of the logarithm of K (ln K) versus the pK(a). Steric hindrance of the polymer chain of 1 on the coordination of the stilbazole residue of (Z)-1 to CoS was thought to cause the small K. A photoresponsive change of apparent oxygen-binding affinity of 1-CoS along with the E/Z isomerization of the stilbazole residues was observed. The ratio of (Z)-1-CoS converted from (E)-1-CoS by the ultraviolet irradiation could be estimated from analysis of absorption spectra for the oxygen binding of a resulting mixture of (E)-1-CoS and (Z)-1-CoS.     

Photosensitized DNA damage and its protection via a novel mechanism

UVA, which accounts for approximately 95% of solar UV radiation, can cause mutations and skin cancer. Based mainly on the results of our study, this paper summarizes the mechanisms of UVA-induced DNA damage in the presence of various photosensitizers, and also proposes a new mechanism for its chemoprevention. UVA radiation induces DNA damage at the 5'-G of 5'-GG-3' sequence in double-stranded DNA through Type I mechanism, which involves electron transfer from guanine to activated photosensitizers. Endogenous sensitizers such as riboflavin and pterin derivatives and an exogenous sensitizer nalidixic acid mediate DNA photodamage via this mechanism. The major Type II mechanism involves the generation of singlet oxygen from photoactivated sensitizers, including hematoporphyrin and a fluoroquinolone antibacterial lomefloxacin, resulting in damage to guanines without preference for consecutive guanines. UVA also produces superoxide anion radical by an electron transfer from photoexcited sensitizers to oxygen (minor Type II mechanism), and DNA damage is induced by reactive species generated through the interaction of hydrogen peroxide with metal ions. The involvement of these mechanisms in UVA carcinogenesis is discussed. In addition, we found that xanthone derivatives inhibited DNA damage caused by photoexcited riboflavin via the quenching of its excited triplet state. It is thus considered that naturally occurring quenchers including xanthone derivatives may act as novel chemopreventive agents against photocarcinogenesis.