Using liquid quenching technique,the change of growth mode of graphite in cast iron melt was analysed.Based on the interface structure theory of crystal growth,the concept of multiplication of spiral growth steps was ...Using liquid quenching technique,the change of growth mode of graphite in cast iron melt was analysed.Based on the interface structure theory of crystal growth,the concept of multiplication of spiral growth steps was advanced and two basic multiplication models were given.It was proposed that multiplication of spiral steps is responsible for the change of growth mode of graphite in cast iron melt.The modifying elements such as Ce promote multiplication of spiral steps,which is regarded as the core of modification.Origination of screw dislocation and branch of the sector blocks in radius direction,both of which are essential to spheroidization of graphite in the melt,are caused by multiplication of spiral steps:and so is thickening of graphite plates.展开更多
Let Ω be a bounded balanced pseudoconvex domain in C^n that admits a plurisubhamonic defining function of class C^2. The authors prove that if f is a spiral-like mapping of type a on Ω, then f can be expressed as a ...Let Ω be a bounded balanced pseudoconvex domain in C^n that admits a plurisubhamonic defining function of class C^2. The authors prove that if f is a spiral-like mapping of type a on Ω, then f can be expressed as a limiting form concerning a Schwarz mapping. Moreover, the characteristics for star-like mappings and spiral-like mappings of type α are obtained. As a direct application, the growth theorem for spiral-like mappings of type α is set up.展开更多
The purpose of the present study was to determine protectivie effects of basic fibroblast growth factor (bFGF) on cochlear neurons and hair cells in vitro and in vivo. In experiment I, cultured spiral ganglion neurons...The purpose of the present study was to determine protectivie effects of basic fibroblast growth factor (bFGF) on cochlear neurons and hair cells in vitro and in vivo. In experiment I, cultured spiral ganglion neurons (SGNs) prepared from P3 mice were exposed to 20mM glutamate for 2 hours before the culture medium was replaced with fresh medium containing 0, 25, 50, and 100 ng/ml bFGF, respectively. Fourteen days later, all cultures were fixed with 4% paraformaldehyde, and stained with 1% toluidine blue. The number of surviving SGNs were counted and the length of SGNs neurites were measured. Exposure to 20 mM glutamate for 24 hours resulted in an inhibition on neurite outgrowth of SGNs and elevated cell death. Treatment of the cultures with bFGF led to promotion of neurite outgrowth and elevated number of surviving SGNs. Effects of bFGF were dose dependent with the highest potency at 100 ng/ml. In experiment Ⅱ, in vivo studies were carried out with guinea pigs in which bFGF or artificial perilymph was perfused into the cochlea to assess possible protective effects of bFGF on cochlear hair cells and compound action potentials(CAP). The CAPs were measured before, immediatly and 48 hours after exposure to noise. Significant differences in CAP were observed (p＜0. 05 ) among the bFGF perfused group, control group(t =3. 896 ) and artificial perilymph perfused group (t =2. 520) at 48 hours after noise exposure, Cochleae were removed and hair cell Loss was analyzed in surface preparations prepared from all experimental animals. Acoustic trauma caused loss of 651 and 687 inner hair cells in the control and artificial perilymph perfused group, respectively. In sharp contrast, only 31 inner hair cells were lost in the bFGF perfused ears. Similarly, more outer hair cells died in the control and perilymph perfuesed group (41830 and 41968, respectively) than in the group treated with bFGF (34258). Our results demonstrate that bFGF protected SGNs against glutmate neurotoxicity in vitro. In addition, treatment with bFGF also protected hair cells from acoustic trauma.展开更多
文摘Using liquid quenching technique,the change of growth mode of graphite in cast iron melt was analysed.Based on the interface structure theory of crystal growth,the concept of multiplication of spiral growth steps was advanced and two basic multiplication models were given.It was proposed that multiplication of spiral steps is responsible for the change of growth mode of graphite in cast iron melt.The modifying elements such as Ce promote multiplication of spiral steps,which is regarded as the core of modification.Origination of screw dislocation and branch of the sector blocks in radius direction,both of which are essential to spheroidization of graphite in the melt,are caused by multiplication of spiral steps:and so is thickening of graphite plates.
文摘Let Ω be a bounded balanced pseudoconvex domain in C^n that admits a plurisubhamonic defining function of class C^2. The authors prove that if f is a spiral-like mapping of type a on Ω, then f can be expressed as a limiting form concerning a Schwarz mapping. Moreover, the characteristics for star-like mappings and spiral-like mappings of type α are obtained. As a direct application, the growth theorem for spiral-like mappings of type α is set up.
文摘The purpose of the present study was to determine protectivie effects of basic fibroblast growth factor (bFGF) on cochlear neurons and hair cells in vitro and in vivo. In experiment I, cultured spiral ganglion neurons (SGNs) prepared from P3 mice were exposed to 20mM glutamate for 2 hours before the culture medium was replaced with fresh medium containing 0, 25, 50, and 100 ng/ml bFGF, respectively. Fourteen days later, all cultures were fixed with 4% paraformaldehyde, and stained with 1% toluidine blue. The number of surviving SGNs were counted and the length of SGNs neurites were measured. Exposure to 20 mM glutamate for 24 hours resulted in an inhibition on neurite outgrowth of SGNs and elevated cell death. Treatment of the cultures with bFGF led to promotion of neurite outgrowth and elevated number of surviving SGNs. Effects of bFGF were dose dependent with the highest potency at 100 ng/ml. In experiment Ⅱ, in vivo studies were carried out with guinea pigs in which bFGF or artificial perilymph was perfused into the cochlea to assess possible protective effects of bFGF on cochlear hair cells and compound action potentials(CAP). The CAPs were measured before, immediatly and 48 hours after exposure to noise. Significant differences in CAP were observed (p＜0. 05 ) among the bFGF perfused group, control group(t =3. 896 ) and artificial perilymph perfused group (t =2. 520) at 48 hours after noise exposure, Cochleae were removed and hair cell Loss was analyzed in surface preparations prepared from all experimental animals. Acoustic trauma caused loss of 651 and 687 inner hair cells in the control and artificial perilymph perfused group, respectively. In sharp contrast, only 31 inner hair cells were lost in the bFGF perfused ears. Similarly, more outer hair cells died in the control and perilymph perfuesed group (41830 and 41968, respectively) than in the group treated with bFGF (34258). Our results demonstrate that bFGF protected SGNs against glutmate neurotoxicity in vitro. In addition, treatment with bFGF also protected hair cells from acoustic trauma.
