BACKGROUND：Live delivery limits the clinical application of maggot therapy. To date in China, there are no in vivo reports regarding wound healing mechanisms of maggot therapy or the effects of maggot homogenate on w...BACKGROUND：Live delivery limits the clinical application of maggot therapy. To date in China, there are no in vivo reports regarding wound healing mechanisms of maggot therapy or the effects of maggot homogenate on wound nerve regeneration.OBJECTIVE：To avoid complications due to the use of live maggots, an aseptic maggot homogenate was applied. Substance P （SP） and gene protein product 9.5 expression in a cutaneous wound was analyzed to explore possible mechanisms of neural regeneration and wound healing in the rat.DESIGN, TIME AND SETTING：A random grouping and controlled animal study was performed at the laboratory of the Department of Orthopedic Surgery, First Affiliated Hospital, Dalian Medical University from August 2008 to April 2009.MATERIALS：Live maggots were cultured and provided by the laboratory of the Department of Orthopedic Surgery of the First Affiliated Hospital, Dalian Medical University, China.METHODS：A total of 48 adult rats were selected and two acute, full-thickness wounds （round, 1.5 cm diameter） were created on the back of each rat. The two wounds were randomly assigned to homogenate product and control groups. Following two-step disinfection of maggots, a homogenate was produced from 10 maggots and applied to the wound area in the homogenate product group, while the wounds in the control group were treated with normal saline alone.MAIN OUTCOME MEASURES：On days 1,3, 7, 10, 14, and 21 following injury, the wound tissue was excised. Histological examination of the wound was observed by hematoxylin and eosin staining or Masson＇s Trichrome staining. SP and protein gene product 9.5 expressions were examined by immunohistochemistry to evaluate wound neural regeneration.RESULTS：On days 7, 10, and 14, the rate of wound healing was significantly greater in the homogenate product group compared with the control group （P 〈 0.05）, and homogenate healing was better than that seen in the control group. On days 3, 7, and 10, SP expression in cells and regenerative nerves was s展开更多
Objective:To carry out an experimental study with the main objective of mass rearing of sheep flies(Lucilia sericata).Methods:Hand collection and beef- or cattle liver-baited net traps were used for field fly sampling...Objective:To carry out an experimental study with the main objective of mass rearing of sheep flies(Lucilia sericata).Methods:Hand collection and beef- or cattle liver-baited net traps were used for field fly sampling from April,2010 to November,2010.The samples collected from different places were placed in properly labeled tubes and sent to the Entomology Laboratory. Since maggot identification is important in inducing mortality,they were kept under insectary condition to develop to adult stage and identified using systematic keys.Results:A total of 218 flies were collected in three rounds of sampling from the field of Tehran and Karaj Counties.In the first generation,433 flies including 135(31.17%) male,and 298(68.82%) female were yielded. The female/male of parent ratio was calculated as 1.72 in Tehran and in Karaj areas,whereas it was 2,20%and 1.81%,respectively in Fl and F2 generations,respectively.Conclusions:During this study,the mass rearing of sheep blow fly has been established at the School of Public Health, Tehran University of Medical Sciences and can be used for producing flies for maggot therapy.展开更多
The developmental rate under low temperatures and cold tolerance were investigated in embryos of the blowfly Lucilia sericata. The larvae of this species are now widely used in maggot debridement therapy. Embryonic de...The developmental rate under low temperatures and cold tolerance were investigated in embryos of the blowfly Lucilia sericata. The larvae of this species are now widely used in maggot debridement therapy. Embryonic development was dependent on temperature, with a lower developmental threshold of 9.0℃. The duration of the egg stage at a rearing temperature of 25℃was 14 h, and a low temperature of 12.5℃ successfully prolonged this period to 66 h. Embryonic stages differed markedly in their cold tolerance; young embryos were less tolerant to cold than old ones. Late embryonic stages are suitable for cold storage at 5℃ and the storage for 72 h did not decrease the hatching rate by more than 50%. In the mass-rearing process required for maggot debridement therapy, either of these two simple protocols would be beneficial.展开更多
基金Supported by the National Natural Science Foundation of China,No. 30873336
文摘BACKGROUND：Live delivery limits the clinical application of maggot therapy. To date in China, there are no in vivo reports regarding wound healing mechanisms of maggot therapy or the effects of maggot homogenate on wound nerve regeneration.OBJECTIVE：To avoid complications due to the use of live maggots, an aseptic maggot homogenate was applied. Substance P （SP） and gene protein product 9.5 expression in a cutaneous wound was analyzed to explore possible mechanisms of neural regeneration and wound healing in the rat.DESIGN, TIME AND SETTING：A random grouping and controlled animal study was performed at the laboratory of the Department of Orthopedic Surgery, First Affiliated Hospital, Dalian Medical University from August 2008 to April 2009.MATERIALS：Live maggots were cultured and provided by the laboratory of the Department of Orthopedic Surgery of the First Affiliated Hospital, Dalian Medical University, China.METHODS：A total of 48 adult rats were selected and two acute, full-thickness wounds （round, 1.5 cm diameter） were created on the back of each rat. The two wounds were randomly assigned to homogenate product and control groups. Following two-step disinfection of maggots, a homogenate was produced from 10 maggots and applied to the wound area in the homogenate product group, while the wounds in the control group were treated with normal saline alone.MAIN OUTCOME MEASURES：On days 1,3, 7, 10, 14, and 21 following injury, the wound tissue was excised. Histological examination of the wound was observed by hematoxylin and eosin staining or Masson＇s Trichrome staining. SP and protein gene product 9.5 expressions were examined by immunohistochemistry to evaluate wound neural regeneration.RESULTS：On days 7, 10, and 14, the rate of wound healing was significantly greater in the homogenate product group compared with the control group （P 〈 0.05）, and homogenate healing was better than that seen in the control group. On days 3, 7, and 10, SP expression in cells and regenerative nerves was s
文摘Objective:To carry out an experimental study with the main objective of mass rearing of sheep flies(Lucilia sericata).Methods:Hand collection and beef- or cattle liver-baited net traps were used for field fly sampling from April,2010 to November,2010.The samples collected from different places were placed in properly labeled tubes and sent to the Entomology Laboratory. Since maggot identification is important in inducing mortality,they were kept under insectary condition to develop to adult stage and identified using systematic keys.Results:A total of 218 flies were collected in three rounds of sampling from the field of Tehran and Karaj Counties.In the first generation,433 flies including 135(31.17%) male,and 298(68.82%) female were yielded. The female/male of parent ratio was calculated as 1.72 in Tehran and in Karaj areas,whereas it was 2,20%and 1.81%,respectively in Fl and F2 generations,respectively.Conclusions:During this study,the mass rearing of sheep blow fly has been established at the School of Public Health, Tehran University of Medical Sciences and can be used for producing flies for maggot therapy.
文摘The developmental rate under low temperatures and cold tolerance were investigated in embryos of the blowfly Lucilia sericata. The larvae of this species are now widely used in maggot debridement therapy. Embryonic development was dependent on temperature, with a lower developmental threshold of 9.0℃. The duration of the egg stage at a rearing temperature of 25℃was 14 h, and a low temperature of 12.5℃ successfully prolonged this period to 66 h. Embryonic stages differed markedly in their cold tolerance; young embryos were less tolerant to cold than old ones. Late embryonic stages are suitable for cold storage at 5℃ and the storage for 72 h did not decrease the hatching rate by more than 50%. In the mass-rearing process required for maggot debridement therapy, either of these two simple protocols would be beneficial.
