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R L Chao

Publications and source records attributed to R L Chao.

2 recordsLinked to original sources

Producing exposed coat-free embryos.

Production of embryos that are free of tough outer coats facilitates studies that are not possible with embryos surrounded by impenetrable envelopes. This report describes a new procedure for preventing formation of fertilisation membranes in the sea urchin (Lytechinus pictus) model. This procedure involves treating unfertilised eggs with the enzyme alpha-amylase, which cleaves alpha-1,4 glucosidic bonds in the vitelline layer. A major advantage of this method is that it is very well defined and completely controllable with alpha-amylase inhibitor. The results suggest that intact alpha-1,4 glucosidic bonds are essential for vitelline layer integrity required for formation of the fertilisation membrane. Eggs treated with alpha-amylase possessed the same surface lectin receptors as untreated eggs and, as shown by light and transmission electron microscopy, produced healthy, cleaving embryos that were free of fertilisation envelopes.

Animals↗

[Study on cryosurvival rate of spermatozoa].

Semen samples obtained from 18 healthy volunteers and 42 subfertile men were divided into four groups: normospermia (n = 18), oligozoospermia (n = 21), asthenozoospermia (n = 10), and oligoasthenozoospermia (n = 11). After semen analysis, 10% glycerol was used as a cryoprotectant and the samples were stored in a liquid nitrogen tank at -196 degrees C. We studied the cryosurvival rate of thawed spermatozoa after cryopreservation at one week and one month. Further comparisons of the cryosurvival rate of spermatozoa thawed at 30 minutes, 60 minutes and 120 minutes were also made. Our results showed that: (1) there was no significant difference in the cryosurvival rate between spermatozoa preserved for one week and those preserved for one month (73.3% vs 68.7%, p greater than 0.05); (2) there was, however, a significant difference in the cryosurvival rate of spermatozoa thawed at 60 minutes and those thawed at 120 minutes (74.3% vs 60.2%, p less than 0.05); and (3) there was a significant difference in the cryosurvival rate of oligozoospermia/normospermia (39.0%) vs 73.3%, p less than 0.05) and oligoasthenozoospermia/normospermia (35.0% vs 73.3%, p less than 0.05). Thus, we suggest that artificial insemination with frozen semen be performed within one hour after thawing and that fresh semen is preferred to frozen semen in oligozoospermia and oligoasthenozoospermia patients undergoing artificial insemination.

Adult↗