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Biomedical subjects

H S Li

Publications and source records attributed to H S Li.

At least 37 records · Page 2Linked to original sources
PubMed1998

Small sensory neurons in the rat dorsal root ganglia express functional NK-1 tachykinin receptor.

The tachykinins substance P (SP) and neurokinin A, released by the C-type primary afferent fibre terminals of the small dorsal root ganglion (DRG) neurons, play important roles in spinal nociception. By means of non-radioactive in situ hybridization and whole-cell recording, we showed that the small rat DRG neurons also express the NK-1 tachykinin receptor. In situ hybridization demonstrated that the positive neurons in rat DRG sections were mainly small cells (85.9%) with diameters less than 25 microm. The remaining positive neurons (14.1%) were cells with medium diameters between 26 and 40 microm. No positive large neurons (diameters > 40 microm) were observed. Expression in small DRG neurons (diameter < 21 microm) was confirmed by in situ hybridization of isolated cells, which were demonstrated to express NK-1 receptor mRNA at a very high frequency (> 90% of small DRG neurons) and therefore were subjected to whole-cell recording. In 57 of 61 cells recorded, SP or the selective NK-1 receptor agonist [Sar9, Met(O2)11]SP (Sar-SP, 1 or 2 microM) produced a delayed vibrating inward current (50-300 nA) with a long duration of 0.5-2 h. These currents were blocked by co-application of the NK-1 receptor antagonist L-668, 169 (1 microM), but were not affected by the NK-2 antagonist L-659, 877 (2 microM). Both current-clamp recording and cell-attached single-channel recording demonstrated that the long-lasting response was due to the opening of a channel with an inward current. Employment of non-Ca2+ and Ca2+ + choline solutions revealed that this channel might be a Ca2+-permeable, non-selective cation channel. The prolonged NK-1 tachykinin response exhibited extreme desensitization. This work suggests that presynaptic NK-1 autoreceptors may be present on the primary afferent terminals in the spinal cord, where they could contribute to the chronic pain and hyperalgesia.

Animals↗
PubMed1997

Coassembly of TRP and TRPL produces a distinct store-operated conductance.

The Drosophila retinal-specific protein, TRP (transient receptor potential), is the founding member of a family of store-operated channels (SOCs) conserved from C. elegans to humans. In vitro studies indicate that TRP is a SOC, but that the related retinal protein, TRPL, is constitutively active. In the current work, we report that coexpression of TRP and TRPL leads to a store-operated, outwardly rectifying current distinct from that owing to either TRP or TRPL alone. TRP and TRPL interact directly, indicating that the TRP-TRPL-dependent current is mediated by heteromultimeric association between the two subunits. We propose that the light-activated current in photoreceptor cells is produced by a combination of TRP homo- and TRP-TRPL heteromultimers.

Animals↗
PubMed1997

Pax-6, Prox 1, and Chx10 homeobox gene expression correlates with phenotypic fate of retinal precursor cells.

PURPOSE: To study the expression patterns of the homeobox genes Pax-6, Prox 1, and Chx10 during chick retinal development in vivo and in vitro. METHODS: Sections of paraformaldehyde-fixed, paraffin-embedded eyes were obtained at a range of developmental stages. In situ hybridization was carried out on tissue sections using digoxigenin-labeled sense and antisense RNA probes that recognize chicken Pax-6 and Prox 1 (whose sequences were already available), and chicken Chx10 (which was cloned and sequenced as part of this study). Selected developmental stages were also studied by immunocytochemistry with antibodies against Pax-6 and Prox 1, and by Northern blot analysis using 32P-labeled probes. RESULTS: Until embryonic day (ED) 5, in situ hybridization shows widespread, diffuse distribution of all three genes. Between ED 6 and ED 8, however, they acquire distinct, topographically specific patterns of expression. The Prox 1 signal is predominantly expressed in the prospective horizontal cell layer of the neuroepithelium, decreases vitreally, and is absent from ganglion cells and the prospective photoreceptor layer. Pax-6 is strongly expressed only in the prospective ganglion-cell and amacrine-cell regions at the same stages, and is not detected in prospective photoreceptors. Chx10 expression becomes concentrated in the future bipolar-cell region of the inner nuclear layer. Similar patterns are maintained by ED 15 through ED 18, after cell differentiation has taken place. Pax-6 and Prox 1 immunoreactive materials showed nuclear localization and a pattern of laminar distribution equivalent to that seen by in situ hybridization. CONCLUSIONS: These results suggest that the differentiated fate of retinal precursor cells may be influenced by Pax-6, Prox 1, or Chx10, this hypothesis is now being tested using dissociated chick embryo retinal cell cultures.

Amino Acid Sequence↗
PubMed1996

[Variability of the parameters of oscillatory potentials of the human electroretinogram].

Oscillatory potentials (OP) of the electroretinogram (ERG) of 20 subjects providing 30 normal eyes were recorded by means of Ganzfeld stimulation at 11 stimulus intensities. It was found that intensity-implicit time functions of the OP components are exponential, while the intensity-response curves are highly variable. The amplitudes of the four wavelets showed relatively large coefficients of variation and intersubject variation, while those of the implicit time are small. Thus it appears that measurement of oscillatory potential implicit time rather than amplitude may provide a more reliable index to access certain retinal condition.

Adult↗
PubMed1995

[Studies on gelatin microspheres-in-oil emulsion of pingyangmycin].

As a drug for lymphosarcoma, pingyangmycin (A5) is not widely used because of its toxicities, short half-life and low affinity to lymph. For the purpose of delivering A5 to the lymph system to strengthen and sustain its effects and to lower its toxicities, its gelatin microspheres-in-oil emulsion (S/O) was studied in vitro and in vivo. By ultrasonication, gelatin microspheres with diameters of 1.67 +/- 0.69 microns were homogeneously dispersed in oil to form the S/O, which was a pseudoplastic flow and stable under 0 degrees C for at least 1 month. With the content of 14.03 +/- 0.15 mg.ml-1, A5 released from the emulsion in a zero order rate with t0.5 of 12.0 h. In vivo experiments showed that the S/O emulsion exhibited potent lymphotropicity, prolonged plasma concentration and a probably lower pulmonary toxicity.

Animals↗
PubMed1994

Pax-6 is first expressed in a region of ectoderm anterior to the early neural plate: implications for stepwise determination of the lens.

The Pax-6 gene encodes a DNA-binding transcription factor essential to normal development of the mammalian eye. We have found that in the chick embryo, the Pax-6 gene is first expressed in a crescent-shaped region of future head ectoderm that adjoins the anterior margin of the early neural plate. As development proceeds, this region of Pax-6-positive ectoderm becomes divided into two bilateral domains. Upon contact with the optic vesicles, portions of these domains give rise to the invaginating lens placodes, which contain high levels of Pax-6 mRNA. As with mouse, rat, and zebrafish, chick Pax-6 is also expressed in the neural epithelium of the forebrain and optic vesicles. However, our results indicate that the onset of expression in the prospective head ectoderm occurs at a substantially earlier stage. Experiments involving unilateral ablation of the anterior neural plate indicate that contact with an optic vesicle is not required to maintain expression of Pax-6 in the ectoderm. Experiments in which optic vesicles have been displaced from their normal location further suggest that positioning of Pax-6 domains in the head ectoderm is independent of neighboring optic vesicles. Homozygous defects in the mouse and rat Pax-6 gene are known to cause complete failure of lens formation at the optic vesicle stage and block subsequent development of the optic cup. Our results raise the possibility that Pax-6 may be involved in the early establishment of lens-competent regions within the head ectoderm.

Amino Acid Sequence↗
PubMed1994

Identification of a glutamate/aspartate transporter in the rat cochlea.

The neurotransmitter at the synapses between hair cells and spiral ganglion cells in the cochlea is probably L-glutamate or a similar excitatory amino acid. Glutamate uptake by nerve terminals and glial cells is an important component of neurotransmission at glutamatergic synapses of the central nervous system, for providing a reservoir of transmitter or transmitter precursors and the termination of the released glutamate. Hair cell synapses are not surrounded by glial cells, therefore, the uptake mechanism for glutamate in the cochlea may be unique. cDNA was synthesized from total RNA isolated separately from the rat organ of Corti, spiral ganglia, and lateral wall tissues. The expression of a glutamate/aspartate transporter (GLAST) was detected by DNA amplification with the polymerase chain reaction. The other two members of glutamate transporters in this family were not detected by this method. A partial cDNA encoding to GLAST was identified by sequence analysis in a rat cochlear cDNA library. Data concerning the expression and the molecular structure of the glutamate transporter GLAST in the cochlea may provide important information regarding the neurotransmission process at the hair cell-afferent synapses.

Amino Acid Sequence↗
PubMed1993

Inner ear morphology in CBA/Ca and C57BL/6J mice in relationship to noise, age and phenotype.

CBA/Ca mice showing moderate hearing losses with onset late in life and C57BL/6J mice with progressive hearing losses starting when animals were young adults were exposed to a 2-7 kHz, 120 dB SPL noise band for 5 min in order to investigate morphological consequences to noise as a function of age and genotype. Permanent threshold shifts were determined by auditory brainstem responses 1 month after noise exposure at 1, 3 and 6 months of age. CBA mice had a decreasing susceptibility to noise with increasing age, while C57 mice remained equally susceptible throughout all ages tested. The threshold shifts were then analyzed in relation to morphological changes of the organ of Corti as visualized by light microscopy (LM), transmission electron microscopy (TEM) and scanning electron microscopy (SEM). CBA mice exposed at 1 month and sacrificed at 2 months had seemingly normal cochlear morphologies under LM. In these animals SEM findings demonstrated mild stereocilia damage to noise trauma, but not when mice were exposed at 3 and 6 months. There was no visible morphological aging of hair cells found during the period tested. In contrast, the C57 mice had early hair cell changes including bent and fused stereocilia, bulging of the cuticular plates, hair cell loss and swelling of afferent dendrites. These changes became more pronounced throughout the test periods with the variability of damage in this strain more evident over time. This pattern was also aggravated in all C57 age groups tested after noise exposure. Quantification with cytocochleograms demonstrated a statistically different reaction pattern to noise trauma between the two different genotypes of mice.

Aging↗
PubMed1993

Auditory degeneration after acoustic trauma in two genotypes of mice.

Two strains of mice, CBA/Ca and C57BL/6J, were exposed to a steady noise (2-7 kHz) of 120 dB SPL for 5 min at 1, 3, 6, or 12 months of age. Threshold shifts were determined by recording auditory brainstem response 1 month after exposure and thereafter up to the age of 16 months (C57BL) or 23-27 months (CBA). With increasing age of exposure, susceptibility to acoustic trauma at middle frequencies (6.3-12.5 kHz) 1 month after exposure decreased in CBA mice but remained constant in C57BL mice. With increasing age after exposure, threshold shifts were retained at the middle frequencies in CBA mice exposed at 1 month of age and in C57BL mice of all exposed groups. The progress of the interaction between the previous noise damage and aging effects was generally the same for the two strains, first an additivity and then a blocking-like interaction. The rate of the progress in post-noise hearing did not exceed the spontaneous rate of aging. The differences between exposed and non-exposed groups decreased with advancing age. The results indicate that the interaction of noise trauma and aging effects depends on the susceptibility of the individual to acoustic trauma, affected frequencies, and the severity of noise-induced PTS. A previous noise damage did not potentiate the auditory degeneration either in CBA/Ca or in C57BL/6J mice.

Acoustic Stimulation↗
PubMed1993

[Epidemiological studies on human cryptosporidiosis in rural and urban areas of Jiangsu].

A survey of cryptosporidiosis in outpatients and inhabitants in Xuzhou city and 6 rural areas of Jiangsu Province was carried out from 1989 to 1991. Cryptosporidium oocysts (CSO) were found in 97 (1.6%) of 6,221 individuals as a whole, and were detected in 39 (3.3%) of 1,172 outpatients among the examinees. 39 cases were from 31 towns and villages of 8 counties near Xuzhou city. Among the 136 cases, 83 were males and 53 females, of them 89 (65.4%) were infants and young children. The incidence was evidently higher in the group of children under 4 than in that aged 4 to 15 (P < 0.01). Diarrhea, intermittent or persistent, was the main symptom of cryptosporidiosis, being present in 94 (69.1%) of the 136 positive cases, while the other 42 were asymptomatic carriers. The results of routine blood examination and immunoassay performed in a part of the infected children indicated that more than half of them had anemia and lessened cellular immunity. Stool examination of the domestic animals of the affected households showed that a pig and a dog were CSO positive.

Adolescent↗
PubMed1992

Auditory degeneration after exposure to toluene in two genotypes of mice.

Two inbred strains of mice, CBA/Ca (with a moderate hearing loss starting late in life) and C57BL/6J (with an early onset of spontaneous auditory degeneration), were exposed to toluene by inhalation (1000 ppm, 12 h/day, 7 days) at either 1 or 6 months of age. Thresholds of auditory brainstem response (ABR) were measured 3-5 days after exposure and assessed repeatedly up to the age of 16 months (C57) or 23 months (CBA). Both strains of mice exposed to toluene at 1 month of age showed a mild loss of sensitivity at a high frequency (31.5 kHz) shortly after exposure. With increasing age, toluene exposure had little effect on the aging process of the auditory system in CBA mice but accelerated age-related hearing loss in C57 mice. The results indicate that toluene exposure can aggravate auditory deterioration only in mice with a strong genetic predisposition to spontaneously precocious age-related hearing loss.

Administration, Inhalation↗
PubMed1992

Cryptosporidium infection and diarrhea in rural and urban areas of Jiangsu, People's Republic of China.

Screening of infants and children under age 15 years for Cryptosporidium oocysts in their stools was carried out in the suburb of Xuzhou City and six rural areas of Jiangsu Province. The infection rate varied from 0.7 to 5.06%. Of the total of 5,089 children examined, 89 (1.75%) were oocyst positive. The incidence was evidently higher in the group of children under age 4 years than it was in children from 4 to 15 years (P less than 0.01). Routine blood examination and immunoassay performed on blood samples from some of the infected children indicated that more than half of them had anemia and lower cellular immunity. Diarrhea was the main symptom of cryptosporidiosis. It was intermittent or persistent and was present in 57 of the 89 children positive for Cryptosporidium oocysts, while the other 32 children were asymptomatic carriers. Examination of stool specimens of adult members and domestic animals of about half of the infected families showed that two mothers, one pig, and one dog were positive for Cryptosporidium oocysts.

Adolescent↗
PubMed1992

Influence of genotype and age on acute acoustic trauma and recovery in CBA/Ca and C57BL/6J mice.

Two inbred strains of mice, CBA/Ca (with a moderate auditory impairment starting late in life) and C57BL/6J (with a progressive auditory degeneration starting during young adulthood), were exposed to a 120 dB SPL broadband noise (2-7 kHz) for 5 min at the age of 1, 3, or 6 months. Compound and permanent threshold shifts (CTS and PTS) were determined by auditory brainstem response during the first day (CTS) and 1 month (PTS) after exposure. With increasing age, susceptibility to CTS at middle frequencies (8 and 12.5 kHz) decreased in CBA mice, yet was retained in C57 mice. C57 mice were more severely affected by CTS than age-matched CBA mice. Noise-induced CTS was positively correlated to pre-exposure thresholds in C57 mice and to PTS over all ages and strains. The amount of recovery from CTS to PTS was, however, independent of age and strain. There was only a 2% risk of classifying CBA mice as C57 mice by pre-exposure thresholds at high frequency, while there was about 40% risk by CTS. The results indicate that genetic predisposition can affect susceptibility to auditory degeneration and noise impairment in a systematic manner, allowing the identification of susceptible individuals by pre-exposure audiometric examination, especially at high frequencies.

Acute Disease↗
PubMed1992

Genetic influences on susceptibility of the auditory system to aging and environmental factors.

Auditory susceptibility to aging and environmental factors (noise and toluene) was investigated in two genotypes of mice, CBA/Ca (showing a moderate hearing loss with onset late in life) and C57BL/6J (undergoing spontaneous auditory degeneration with onset during young adulthood). Both strains of mice were often used together as a model of human age-related hearing loss, with a primary decline in auditory high-frequency sensitivity. Auditory function was analysed by recording auditory brainstem response (ABR). Morphological alterations of mouse cochleae were studied by light, transmission and scanning electron microscopy. The age-related elevation of ABR thresholds was more precipitous and the individual variability was larger in C57BL mice than that in CBA mice. Degeneration patterns of the organ of Corti were different between the two strains. In the old CBA-mouse cochlea, giant stereocilia on the inner hair cells (IHCs) and elevated pillar heads were evident. Some normal-looking outer hair cells (OHCs) still remained. In C57BL mice, however, early loss of OHCs and extensively damaged stereocilia constituted the primary lesions of the organ of Corti. After exposure to a 2-7 kHz steady noise of 120 dB SPL for 5 min at the age of 1, 2, 3, 6, or 12 (only for CBA) months, compound and permanent threshold shifts (CTS and PTS) at middle frequencies (8-12.5 kHz) reduced with age in CBA mice but remained in C57BL mice. C57BL mice were more severely affected by noise than the age-matched CBA mice. The amount of recovery from CTS to PTS was, however, independent of age and strain. Pathological changes of the organ of Corti were correlated with noise-induced PTS. Possibilities for prediction of susceptible individuals were tested. At 6 months of age, there was only 2% risk of classifying C57BL mice as CBA mice by pre-exposure thresholds at the high frequency (31.5 kHz), but about 40% risk by CTS at the middle frequency (12.5 kHz), or vice versa. With increasing age, the progress of the interaction between noise trauma and aging had two phases for both strains of mice. First an additivity and then, at total threshold shifts of 30-50 dB, a blocking-like interaction were observed. The rate of progression in post-noise hearing loss did not exceed the spontaneous rate of age-related degeneration. The difference between exposed and non-exposed groups decreased with advancing age for both strains of mice.(ABSTRACT TRUNCATED AT 400 WORDS)

Acoustic Stimulation↗
PubMed1991

Age-related loss of auditory sensitivity in two mouse genotypes.

Frequency-specific auditory brainstem responses (ABR) (frequency range 2-31.5 kHz) were used to describe age-dependent alterations in frequency sensitivity in CBA/ca (to 30 months) and C57BL/6J (to 16 months) mouse genotypes. The two strains displayed an age-related loss similar to that of humans, with a primary decline in high-frequency sensitivity. CBA mice showed a slow, yet gradual decrease in sensitivity to high- followed by low-frequency until 18 months of age and a rapid deterioration at all frequencies thereafter. C57 mice demonstrated precocious aging in auditory sensitivity in an unsteady rather than gradual manner. By testing the same individuals on repeated occasions it was shown that, for C57 mice, the degenerative process was more precipitous with three phases, and that the individual variability was larger than that of CBA mice. It is suggested that the two mouse genotypes can be used to express the different aspects of human presbycusis in individual variability and modes of gradual or staggered progression.

Aging↗
PubMed1991

[Effects of AMG-1 on energy metabolism and neuronal damage of ischemic brain in mice and rats].

The effect of AMG-1 [6(5-hydroxy-2-methylpyridylamino)-9 ribofranosylpurine] on mouse brain energy metabolism in complete brain ischemia induced by decapitation and on neurological deficit and histopathological changes after occlusion of the middle cerebral artery (MCAO) in rats were studied. The results indicate that AMG-1 has an effect of improving the status of energy metabolism in complete brain ischemia in mice. Lactate concentration was greatly reduced and the ATP and phosphocreatine levels were significantly elevated. Treatment with AMG-1 or nimodipine was performed before and after MCAO. The score of neurological deficit was significantly decreased as compared with the vehicle treated group. The extent of ischemic neuronal injury was determined by histopathological examination. AMG-1 and nimodipine seemed to attenuate the MCAO-induced neuronal damage. In as much as AMG-1 can improve the status of brain energy metabolism, neurological deficit and neuronal damage after ischemic insult, AMG-1 may have a beneficial effect for the treatment of cerebral ischemic damage.

Adenosine↗