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Chunhua Hu

Publications and source records attributed to Chunhua Hu.

11 recordsLinked to original sources

Phospholipases A2 mediate amyloid-beta peptide-induced mitochondrial dysfunction.

Mitochondrial dysfunction has been implicated in the pathophysiology of Alzheimer's disease (AD) brains. To unravel the mechanism(s) underlying this dysfunction, we demonstrate that phospholipases A2 (PLA2s), namely the cytosolic and the calcium-independent PLA2s (cPLA2 and iPLA2), are key enzymes mediating oligomeric amyloid-beta peptide (Abeta(1-42))-induced loss of mitochondrial membrane potential and increase in production of reactive oxygen species from mitochondria in astrocytes. Whereas the action of iPLA2 is immediate, the action of cPLA2 requires a lag time of approximately 12-15 min, probably the time needed for initiating signaling pathways for the phosphorylation and translocation of cPLA2 to mitochondria. Western blot analysis indicated the ability of oligomeric Abeta(1-42) to increase phosphorylation of cPLA2 in astrocytes through the NADPH oxidase and mitogen-activated protein kinase pathways. The involvement of PLA2 in Abeta(1-42)-mediated perturbations of mitochondrial function provides new insights to the decline in mitochondrial function, leading to impairment in ATP production and increase in oxidative stress in AD brains.

Amyloid beta-Peptides↗

Synthesis, crystal structure, and properties of MnNCN, the first carbodiimide of a magnetic transition metal.

Synthesis, single-crystal structure determination, and magnetic properties are reported for manganese carbodiimide, MnNCN. The presumably unstable but inert phase adopts the trigonal system (R3m) with a = 3.3583(4) A, c = 14.347(2) A, V = 140.13(3) A3, and Z = 3. Divalent manganese is octahedrally coordinated by nitrogen atoms at 2.26 A, and the NCN(2-) unit adopts the linear [N=C=N](2-) carbodiimide shape with two C=N double bonds of 1.23 A. MnNCN contains high-spin Mn(II) with five unpaired electrons and behaves like an antiferromagnet with an ordering temperature below 30 K.

Journal Article↗

Formation of complex three- and one-dimensional interpenetrating networks within carbodiimide chemistry: NCN2(-)-coordinated rare-earth-metal tetrahedra and condensed alkali-metal iodide octahedra in two novel lithium europium carbodiimide iodides, LiEu2(NCN)I3 and LiEu4(NCN)3I3.

Orange-red transparent single crystals of LiEu2(NCN)I3 and LiEu4(NCN)3I3 were synthesized from fluxes of europium iodide, sodium cyanide, sodium azide, and lithium iodide at elevated temperatures and structurally characterized by X-ray diffraction. While LiEu2(NCN)I3 crystallizes in the cubic system (Fdm, a = 15.1427(17) angstroms, V = 3472.2(7) angstroms3, Z = 16, R1 = 0.0322), LiEu4(NCN)3I3 adopts the hexagonal system (P6(3)/mmc, a = 10.6575(11) angstroms, c = 6.8232(10) angstroms, V = 671.16(14) angstroms3, Z = 2, R1 = 0.0246). Both extended structures are composed of complex frameworks built from europium tetrahedra coordinated by carbodiimide (symmetrical NCN2-) units on the one side and condensed iodine octahedra around lithium cations on the other. Within LiEu2(NCN)I3, vertex-sharing of the LiI6 subunits together with isolated europium tetrahedra results in two three-dimensional networks interpenetrating each other. Within LiEu4(NCN)3I3, face-sharing of the europium tetrahedra results in bitetrahedral units which further connect via two opposing vertexes into one-dimensional linkages. Likewise, the LiI6 octahedra share common faces to also yield one-dimensional linkages that fill the channels between the europium/carbodiimide substructure. The magnetic behavior of both compounds has been determined; the two phases follow Curie-Weiss laws with weak predominantly ferromagnetic exchange between the europium ions and atomic moments characterizing them as essentially divalent.

Journal Article↗

Unprecedented reactivity of the bridged borylene complexes [mu-BCl((eta(5)-C(5)H(4)Me)Mn(CO)(2))(2)] toward pyridine.

The reactivity of the bridged chloroborylene complex [mu-BCl((eta(5)-C(5)H(4)Me)Mn(CO)(2))(2)] (1) toward pyridine was investigated under various conditions. In the presence of protic reagents such as H[Co(CO)(4)] or H[BF(4)], the formation of the aminoborylene complex [1-(mu-B)-4-H-(NC(5)H(5))((C(5)H(4)Me)Mn(CO)(2))(2)] (2) was observed. Compound 2 represents the product of an unprecedented formal 1,4-hydroboration of pyridine. Corresponding reactions of 1 with pyridine and Tl[PF(6)] afforded 2 in similar yields, thus providing evidence that the abstraction of the boron bound chloride initiates the observed reaction. Complex 2 was fully characterized in solution and in the crystal.

Journal Article↗

Quantitative determination of Aconitum alkaloids in blood and urine samples by high-performance liquid chromatography.

An HPLC method has been developed for the simultaneous determination of the toxic Aconitum alkaloids, aconitine, mesaconitine and hypaconitine in blood and urine samples. The samples were initially subjected to solid phase extraction using Oasis MCX cartridges, and the alkaloids were separated on an XTerra RP18 column, gradient-eluted with acetonitrile: ammonium hydrogen carbonate buffer. Calibration curves were linear in the range 2.75-550 ng for aconitine and hypaconitine, and 3-600 ng for mesaconitine: the limit of detection was 0.1 ng (signal-to-noise ratio of 3) for each alkaloid. The described analysis proved to be sensitive, rapid and economical, and will be applied in the identification and determination of these alkaloids in forensic and therapeutic drug monitoring.

Aconitine↗