麝鼠香腺泌香的组织学观察

应用光学显微镜和电子显微镜技术,观察了麝鼠(Onda zibethica)香腺囊的组织结构,证明香腺由腺细胞、支持细胞和排香管组成。顶浆分泌方式泌香。简述了各级排香管的细胞结构及功能,为建立麝鼠人工活体取香和体外泌香奠定了组织学基础。     

麝鼠香腺发育与活体取香的初步研究

根据麝鼠香腺的形态发育,将其划分为非泌香期、香腺发育期、泌香盛期和泌香持续期４个时期．通过对１９２只成年雄性麝鼠分另进行５次活体取香,每只取香量累计达２．６５±０．３２ｇ。非泌香期肌注丙酸睾丸素５ｍｇ／ｋｇ。可诱导雄麝鼠香腺的发育和泌香。通过饲养繁殖观察,证明雄体取香对配偶雌体繁殖无不良影响。     

冬季肌注丙酸睾丸素和补加光照对麝鼠香腺的影响

冬季每日5mg剂量丙酸睾丸素连续肌注25天,可使成年雌雄麝鼠香腺增大、增重,腺泡细胞增多和成熟;雄激素通过控制腺泡细胞的分裂分化和生长发育直接调节香腺的体积、重量以及分泌活动。冬季递增补加光照60天,每日3小时20分至5小时39分,强度平均为187勒克斯,可使育成雄鼠(4—6月龄)的睾丸、香腺增大、增重;光周期可能通过下丘脑-垂体-睾丸轴系间接影响香腺。     

麝鼠香腺发育及腺细胞培养分离的初步研究

目前麝鼠香是麝香最好的天然替代物,麝鼠香来源于麝鼠生殖系统中的香腺,已发现其香腺中分泌细胞和支持细胞是麝鼠泌香的关键。本研究通过组织形态、HE染色、免疫组织化学染色及免疫荧光鉴定方法,初步描述了麝鼠香腺的发育过程。麝鼠香腺的形态结构显示其由小到大再至非泌香期萎缩;HE染色及组化结果显示,香腺在发育初期富含颗粒饱满的腺泡,雄激素分泌处于较低水平,分泌细胞数量较少,随着进一步发育,雄激素水平及分泌细胞数量逐渐升高,在两个月时达到最高,腺泡逐渐变大成熟并开始释放麝鼠香等分泌物;在泌香末期,腺泡逐渐被结缔组织取代。以上结果将有助于麝鼠香腺发育及分泌机制的研究,为提高麝香产量及实现体外泌香建立基础。另外,我们成功分离并鉴定了分泌细胞和支持细胞,以期为后续建立体外泌香体系奠定基础。     

麝鼠泌香期香囊腺形态及组织结构的研究

麝鼠香囊腺由腺细胞、支持细胞和排香管组成。其分泌腺属复管泡状腺。发育初期的腺泡胞质内含有大量的粗面内质同、光滑内质网、高尔基复合体、中心粒和线粒体、香腺细胞间连接发达,桥粒、半桥粒广为分布。胞质内含有电子致密度高和电子致密度低的两种分泌颗粒。其分泌方式为顶浆分泌。     

麝鼠前列腺在繁殖期和非繁殖期转录组差异分析

麝鼠(Ondatra zibethicus L.)是季节性繁殖动物。成年雄性麝鼠在尿生殖孔上方肌肉与背皮之间有一对香腺,在繁殖期能分泌麝鼠香。与其他鼠类相比,麝鼠在繁殖期时前列腺—精囊腺组织极其发达。研究发现,经腹腔注射麝鼠香后,能够明显促进雄性小鼠的前列腺—精囊腺发育,表明两者之间可能存在一定的相关性。本研究利用RNA-seq技术对麝鼠繁殖期和非繁殖期的前列腺样品进行了转录组测序,对差异表达的基因进行GO分析和KEGG通路分析。结果显示,共筛选出1629个显著差异表达基因,涉及多种信号转导和能量代谢相关基因,其中OBP2、Bcl-2家族和肿瘤坏死因子受体超家族成员的差异表达提示麝鼠前列腺发育受多种机制调控,由香腺分泌的麝鼠香可能参与了前列腺的发育调节。     

GnRH-A主动免疫家兔的去势效果

为了探讨促性腺激素释放激素类似物(gonadotropin releasing hormone analogue,GnRH-A)对动物免疫去势的效果及作用机理.在30只日本大耳白兔(Oryctolagus cuniculus)(EG-Ⅰ与EG-Ⅱ组)的颈背部皮下分2.3点注射1.0ml(100/gml)自制的GnRH-A抗原乳剂,EG-Ⅱ组3周后加强免疫一次;测定睾丸长度与重量、体重、血清GnRH抗体效价及睾酮浓度.结果表明,EG-Ⅱ组睾丸长度与EG-I组差异极显著(P<0.01);EG-Ⅱ组的GnRH抗体水平明显高于EG-Ⅰ组;EG-Ⅱ组、EG-Ⅰ组与对照组的血清睾酮浓度差异逐渐增加,102 d时EG-Ⅱ组睾酮浓度极显著低于对照组(P<0.01),且第28 d后EG-Ⅱ组睾酮浓度显著低于EG-Ⅰ组(P<0.05);EG-Ⅱ组体重和日增重最大,显著高于EG-Ⅰ组及对照组(P<0.05).GnRH-A主动免疫家兔对睾丸发育、血清GnRH抗体效价和睾酮浓度具有显著的影响,加强免疫效果更理想.     

外源性睾酮对去睾丸家兔性激素以及血脂和载脂蛋白水平的影响

目的 :探讨不同剂量的外源性睾酮对去势 (双侧睾丸切除 )雄性家兔性激素以及血脂和载脂蛋白水平的影响。方法 :成熟雄性新西兰白兔 40只 ,随机分成 5组 (n =8) :对照组、单纯去势组、低睾酮血症组 [去势后肌注十一酸睾酮 (TU) ,3mg/kg ,每 2周一次 ]、生理水平组 (去势后肌注TU ,6mg/kg ,每 2周一次 )及高睾酮血症组 (去势后肌注TU ,1 2mg/kg ,每 2周一次 )。 8周后测量血清总睾酮 (TT)、雌二醇 (E2 )、脱氢表雄酮 (DHEA)及总胆固醇 (TC)、高密度脂蛋白胆固醇 (HDL C) ,低密度脂蛋白胆固醇 (LDL C) ,甘油三酯 (TG) ,载脂蛋白A1 (ApoA1 ) ,载脂蛋白B(ApoB)。结果 :雄兔血清TT水平在去势后明显下降至极低水平 ,明显低于对照组 (P <0 .0 1 ) ,3mg/kgTU补充后轻度升高 ,仍明显低于对照组 (P <0 .0 1 ) ,形成低睾酮血症 ,6mg/kgTU补充后与对照组相比无显著差异 (P >0 .0 5) ,接近生理水平 ,1 2mg/kgTU补充后明显高于对照组和低睾酮血症组 (P均 <0 .0 1 ) ,形成高睾酮血症。血清E2 水平在对照组和生理水平组相近并且最低 ,单纯去势组和低睾血症组相近 ,高睾酮血症组最高。E2 /TT比值在对照组和生理水平组相近并且最小 ,在单纯去势组最大 ,低睾酮血症组大于高睾酮血症组。单纯去势组、低睾酮血症组和高睾酮血症     

睾酮对去睾丸家兔骨密度及血清钙磷的影响

目的:观察去睾丸和睾酮补充对雄兔骨密度和血清钙、镁、磷的影响.方法:周龄相同的雄性新西兰白兔随机分成对照组、去睾丸组和睾酮补充组(去睾丸后肌注十一酸睾酮).同等条件下饲养20周后测量各组兔全身骨密度、腰椎骨密度、股骨颈骨密度,并检测血清总睾酮(TT)、雌二醇(E2),脱氢表雄酮(DHEA)水平以及血清钙(Ca2 )、游离钙([Ca2 ]i)镁(Mg2 )、磷(P)和碱性磷酸酶(AKP)浓度.结果:去睾丸组血清TT水平明显下降(P<0.01),睾酮补充组血清TT水平升高接近对照组(P>0.05).去睾丸组血清E2和E2/TT比明显高于对照组(P<0.01),睾酮补充组血清E2和E2/TT下降,接近对照组水平(P均>0.05).与对照组相比,去睾丸组血清Ca2 、[Ca2 ]i、Mg2 以及AKP浓度明显升高(P均<0.01),睾酮补充组血清Ca2 、[Ca2 ]i、Mg2 以及AKP浓度较去睾丸组低,接近对照组水平(P>0.05).股骨颈骨密度在去睾丸组明显低于对照组和睾酮补充组(P<0.01),而后两组无差别(P>0.05).结论:去睾丸后雄兔血清TT明显下降,E2和E2/TT比以及Ca2 、[Ca2 ]i、Mg2 和AKP浓度明显升高,骨密度显著下降,睾酮补充使上述异常明显改善.     

不同移植部位对成年大鼠睾丸间质细胞雄激素分泌功能的影响

目的:探索不同移植部位对移植的成年SD大鼠睾丸中睾丸间质细胞存活及雄激素分泌功能的影响。方法:将健康成年雄性SD大鼠随机分为对照组、假手术组、皮下组和肾包膜组。对照组大鼠不去势,其余大鼠于睾丸移植前1周行去势手术。对照组和假手术组去势后仅行背部皮肤切开,不进行睾丸移植;皮下组背部两侧各移植1/3个成年SD大鼠睾丸组织;肾包膜组每侧肾包膜下移植1/3个成年SD大鼠睾丸组织。4周后取材行HE和免疫组化染色,分析移植睾丸组织中睾丸间质细胞存活情况,ELISA法检测受体大鼠血清睾酮水平。结果:皮下组和肾包膜组移植物中难于见到完整的睾丸间质组织,但免疫组化染色发现大量HSD-17β1阳性细胞,对照组、皮下组和肾包膜组的HSD-17β1阳性细胞数分别为(24.33±4.30)、(9.83±4.05)和(12.67±2.81)个,对照组与皮下组相比差异具有统计学意义(p0.05);ELISA分析发现对照组、假手术组、皮下组和肾包膜组的血清睾酮浓度分别为(3.81±1.32)、(0.28±0.08)、(0.44±0.13)和(0.90±0.31)ng/m L,肾包膜组血清睾酮浓度高于假手术组(p0.01)和皮下组(p0.05),而皮下组血清睾酮水平高于假手术组,但两者差异无统计学意义(p0.05)。结论:移植的成年大鼠睾丸组织中的睾丸间质细胞可在受体肾包膜下或皮下存活,但肾包膜下移植可能更加有利于睾丸间质细胞存活和雄激素分泌。     

麝鼠肠道纤维素分解菌的分离鉴定及其酶学特性分析

本研究旨在从麝鼠(Ondatra zibethicus)肠道中分离出高效分解纤维素的菌株,为开发纤维素分解菌微生物制剂提供菌种资源。本研究利用以羧甲基纤维素钠(CMC-Na)为单一碳源的培养基,从麝鼠盲肠内分离出--株高效分解纤维素的菌株WJ-3,并对该菌株进行形态鉴定、生理生化鉴定和16S.rDNA分子鉴定。对菌株WJ-3所产羧甲基纤维素酶(CMCase)进行酶学特性实验,分析此纤维素酶的最佳反应pH和最佳反应温度,以及此纤维素酶对不同温度和不同酸碱度的耐受性。结果表明,菌株WJ-3属于空气芽孢杆菌(Bacillus aerius),并将其命名为Bacillus aerius WJ-3。菌株WJ-3所产羧甲基纤维素酶在pH 4.0~6.0的范围内反应时,酶活性随pH值升高而增加,其最佳反应pH为6.0,且此纤维素酶在pH4.0~8.0范围内保存30min后均能保持80%以上的相对酶活性:菌株WJ-3所产羧甲基纤维素酶在温度30~50 ℃范围内反应时,随温度上升酶活性逐渐增加,在50 ℃时酶活性最高,之后随温度的升高酶活性逐渐下降,且纤维素酶在此温度范围内保存30 min后均能保持较高的酶活性。综上所述,菌株Bacillus aerius WJ-3所产羧甲基纤维素酶的酶活性较高,并且此纤维素酶的耐酸碱性及热稳定性良好,是具有一定利用价值的菌种资源。     

Body mass and correlated ecological variables in the North American muskrat lineage: evolutionary rates and the tradeoff of large size and speciation potential

This study tracks evolutionary change in body mass (W) and correlated ecological variables over the 3.75 million year history of the North American muskrat (Ondatra zibethicus). A new model is presented suggesting muskrat body mass has been in equilibrium for most of its history. Four pulses of pronounced size increase are correlated with glacial dynamics and volcanic events. Ranges of evolutionary rates in darwins and a new metric based on percent change in W document episodic size change. Proportional size change is independent of interval length, with a background range attributed to natural selection ≤25–30%. In increasing body mass by a factor of ten to about 1 kg mass-specific metabolism was halved, home range quadrupled, population density decreased fourfold, and average biomass more than doubled. Estimates of species diversity in ancient cotton rats (Sigmodon) and muskrats are calculated from a function derived from the correlation of numbers of North American rodent species and mean W. The phyletic mode of muskrat body size increase is explained as a combination of large body size reducing speciation coupled with an aquatic lifestyle. To the ecological consequences of large size in evolving clades (Cope’s rule) we can now add reduced speciation potential.     

Male-biased reproduction and sex-ratio adjustment in muskrats

Summary Sex ratios of a population and of litters were sampled in muskrats in Ontario, Canada. Sex ratios of litters sampled from nests were male biased (54% male). Until weaning, no differential costs of producing and rearing male and female young were identified that could account for this greater production of males. Following weaning, however, male-biased dispersal of juveniles from their natal site and more frequent acquisition by females of these sites as breeding sites the following year suggested a greater investment by adult females in female young. Therefore, competition between female siblings for the acquisition of their natal site may be sufficient to result in the greater production of males. In addition, the simultaneous occupation of, and competition between, siblings and parents for the resources of the natal home range may not be necessary for local resource competition to result in a greater production of the dispersing sex. Greater-than-expected binomial variance in sex ratios of litters suggested that adjustment of sex-ratios occurred. However, we were unable to associate the adjustment of litter sex ratios with changes in maternal condition. The greater production of males and the predominance of monogamous associations between adults in this population may have lead to slightly greater variation in male fitness than female fitness. Therefore, a female in better-than-average condition may have benefited by producing more males. Similarly, a lower cost of producing dispersing males may allow nutritionally-stressed females to reduce their total expenditure on offspring by producing more males. Because these experiments were non-manipulative, maternal condition may not have varied sufficiently during this study to detect adjustments of litter sex ratios resulting from either of the above mechanisms acting separately, but the combined effects of small differences in matermal condition and selective pressures operating in the same direction may have resulted in the observed deviation from the binomial.     

Multiple effects of land‐use changes impede the colonization of open water in fen ponds

Question: Dutch fen areas have become embedded in intensively used landscapes, resulting in biodiversity loss. Hence, plant species that colonize open water inducing the formation of species‐rich floating peat mats have disappeared. Despite many restoration efforts, they have not returned. Is natural succession towards floating mats impeded by site conditions, dispersal limitations or changed biotic interactions? Location: Six Dutch fen reserves: De Deelen, De Weerribben, De Wieden, Westbroek, Molenpolder and Terra Nova. Methods: In 62 fen ponds we determined plant species richness and expansion into open water. We related these to habitat quality (chemical composition of soil and surface water, pond morphology), dispersal potential (distance to remnant populations, likelihood of dispersal) and biotic interactions (presence of muskrats [Ondatra zibethicus L.] and the keystone species Stratiotes aloides). Results: Factor analysis showed that plants expanded further into open water and bank vegetation had higher species richness in areas with older ponds and lower muskrat densities. Locally, high turbidity hampered colonization. Whenever the water was clear, colonization was higher in shallow ponds, and in deep ponds only if Stratiotes was present. Species richness was negatively correlated to nutrient availability in soil and positively correlated to hydrological isolation (decreased sulphate concentrations). We also found that species richness was higher in sheltered banks. Conclusions: Multiple habitat characteristics (turbidity, water depth, nutrient and sulphate concentrations) and the influence of muskrats and Stratiotes all play a role in the lack of restoration success in Dutch fen ponds. Dispersal limitations seem to be overruled by habitat limitations, as colonization often fails even when sufficient propagule sources are present, or when connectivity is high.     

Heat increment of feeding and its thermoregulatory benefit in the muskrat (Ondatra zibethicus)

The calorigenic effect of feeding and its potential benefit in defraying thermoregulatory costs and attenuating immersion hypothermia of adult muskrats were investigated. A single session of feeding on aquatic vegetation was sufficient to raise the metabolic rate of muskrats for a period of at least 5 h. The peak postprandial rate of oxygen consumption averaged 1.42 times the level established for fasted animals, and the heat increment of feeding accounted for about 40% of the metabolizable energy intake of muskrats. There was no evidence of a postprandial rise in oxygen consumption of muskrats that entered water at 18–19°C after feeding. In aquatic trials, average and minimum steady-state oxygen consumption rates of fed muskrats were similar to, or even lower than values recorded from fasted animals, implying substitution of heat increment of feeding for thermoregulatory heat production. Our data did not support the hypothesis that heat increment of feeding retards body cooling in water. Net body temperature decline in water was actually higher in fed animals than in fasted controls. However, since previously fed muskrats also entered water at an elevated body temperature, the final body temperature (at 30 min immersion) was similar in all groups. These findings suggest that metabolic heat generated incidental to preimmersion feeding could provide a thermoregulatory benefit to muskrats by reducing the need for active thermogenesis in water.     

Seasonal changes in the oxygen storage capacity and aerobic dive limits of the muskrat (Ondatra zibethicus)

Summary The oxygen storage capacity and partitioning of body oxygen reserves were compared in summer-and winter-acclimatized muskrats (Ondatra zibethicus). Blood volume, blood oxygen capacity, and skeletal muscle myoglobin content were higher in December than in July (P<0.02). Total lung capacity increased only slightly in winter (P>0.05). The oxygen storage capacity of a diving muskrat was calculated at 25.2 ml O₂ STPD · kg^-1 in July, compared to 35.7 ml O₂ STPD · kg^-1 in December. Blood comprised the major storage compartment in both seasons, accounting for 57% and 65% of the total oxygen stores in summer and winter, respectively. Based on available oxygen stores and previous estimates of the cost of diving, the aerobic dive limit (ADL) increased from 40.9 s in July to 57.9 s in December. Concurrent behavioral studies suggested that most voluntary diving by muskrats is aerobic. However, the proportion of dives exceeding the calculated ADL of these animals was shown to vary with the context of the dive. Only 3.5% of all dives initiated by muskrats floating in the water exceeded their estimated ADL. Provision of a dry resting site and access to a submerged food source increased this proportion to 18–61%, depending on the underwater distance that foraging muskrats were required to swim. Serial dives exceeding the estimated ADL were not accompanied by extended postdive recovery periods.Abbreviations ADL acrobic dive limit - Hb hemoglobin - Hct hematocrit - Mb myoglobin - PaO₂ arterial O₂ tension - STPD standard temperature and pressure, dry