保护酶系在小菜蛾对阿维菌素抗性中的作用

对小菜蛾Plutella xylostella(L.)阿维菌素敏感(ABM-S)和抗性(ABM-R)种群的保护酶系(超氧化物歧化酶SOD、过氧化物酶POD和过氧化氢酶CAT)进行了活性比较。以单头虫表示酶活力,上述3种酶的活性与虫龄正相关,老熟幼虫期酶活性最高。总体上,ABM-S种群的3种酶活性高于ABM-R种群,SOD活性的种群差异随虫龄的增长而减小,1～2龄幼虫ABM-S种群的SOD活性是ABM-R种群的14.27倍。POD活性在3龄幼虫期性差异最大,为4.80倍。CAT活性在4龄末期幼虫无种群差异,其它龄期的活性差异约1～2倍。上述结果表明,阿维菌素抗性并未导致小菜蛾保护酶系统活性增加,这也暗示了昆虫酶系统的能量保守性。     

氰氟虫腙对小菜蛾阿维菌素抗性和敏感种群的亚致死效应(英文)

在实验室条件下采用生命表技术研究了氰氟虫腙亚致死剂量（LC₂₅）对小菜蛾Plutella xylostella阿维菌素抗性（AV-R）和敏感（AV-S）种群的亚致死效应, 旨在为小菜蛾对阿维菌素的抗性治理提供理论基础。结果表明： 氰氟虫腙对小菜蛾3龄幼虫抗性种群的LC₅₀和LC₂₅分别为0.24 mg/L和0.09 mg/L; 对敏感种群的LC₅₀和LC₂₅分别为0.20 mg/L和0.07 mg/L。氰氟虫腙亚致死剂量0.09 mg/L 处理小菜蛾后, 对处理代的影响表现为显著降低处理种群的化蛹率、 蛹重、 羽化率、 繁殖力; 明显延长蛹期, 缩短成虫产卵期和寿命; 对子代种群的影响表现为显著降低卵的孵化率、 幼虫各龄期的存活率, 延长发育历期。处理种群的内禀增长率（r_m）、 周限增长率（λ）和净增值率（R₀）显著低于对照种群（P<0.0001）。亚致死剂量的氰氟虫腙对小菜蛾抗性种群的影响大于敏感种群, 对处理代种群的影响大于子代种群。氰氟虫腙亚致死剂量可以极大地影响小菜蛾尤其是阿维菌素抗性种群的种群动态, 因此氰氟虫腙对于小菜蛾的抗性治理具有积极的作用。     

高温对抗性和敏感小菜蛾生命表参数及后代杀虫剂敏感性的影响

为研究高温对抗性和敏感小菜蛾Plutella xylostella生物学适合度及抗药性进化的影响,本研究测定了温度对杀虫剂抗性和敏感小菜蛾实验种群生命表参数及后代对阿维菌素敏感性的影响。 结果表明：与25℃相比,33.5℃条件下抗性和敏感种群的平均世代历期（D）、净生殖率（R₀）、内禀增长率（r_m）、周限增长率（λ）值、总产卵量、雌蛾平均寿命、日产卵量和孵化率均显著下降。 在25℃下,抗性和敏感种群的r_m,λ,D和日产卵量无显著差异,但抗性种群的R₀略低于敏感种群（为敏感种群的87%）。 在33.5℃下,抗性种群的r_m和R₀显著低于敏感种群（分别为敏感种群的75%和64%）,抗性种群雌成虫寿命、总产卵量和孵化率显著也低于敏感种群。 抗性种群在33.5℃下饲养一代后,后代对阿维菌素的抗性水平大幅下降,而相同处理下敏感种群对阿维菌素的抗性水平没有显著下降。 上述结果表明,无论在常温还是高温条件下,抗性种群生物学适合度均低于敏感种群,尤其是高温下抗性种群适合度远低于敏感种群。 抗性种群经高温饲养一代后对阿维菌素的抗性水平大幅下降可能与高温下抗性种群适合度显著较低有关。     

高效氯氰菊酯对小菜蛾阿维菌素抗性、敏感种群的亚致死效应

在实验室条件下研究了高效氯氰菊酯亚致死剂量LC10 (43.44 mg/L)(小菜蛾阿维菌素抗性种群)和LC10( 12.61 mg/L)(敏感种群)对小菜蛾阿维菌素抗性(AV - R)、敏感(AV -S)种群的亚致死效应.结果表明:高效氯氰菊酯亚致死剂量12.61 mg/L处理小菜蛾阿维菌素敏感、抗性种群3龄幼虫后,...     

敲减人MCHR2基因抑制CHO细胞的放射性 配体受体结合能力及Ca 2+释放

研究人黑色素浓集激素受体2(MCHR2)基因特异的小发夹RNA(shRNA)真核表达载体pGenesil-1-MCHR2-shRNA对MCHR2表达及特征的影响.将pGenesil-1-MCHR2-shRNA转染到稳定表达人MCHR2基因的CHO细胞中,通过RT-PCR和 Western印迹检测MCHR2表达的变化;放射性配体结合实验（RBA）检测受体最大结合容量B _max及平衡解离常数K_d值的变化;钙流检测实验观察配体MCH刺激后单个细胞Ca ²⁺释放及MCH半数有效浓度EC₅₀的变化.与转染pGenesil-1空载体组比较,pGenesil-1-MCHR2-shRNA 能使MCHR2基因mRNA表达减少45.8％～66.4％;蛋白表达减少44.2％～81.0％; B _max减少39.4％～78.7％,K_d值升高40.9％～81.9％;EC ₅₀升高114.8％～822.4％.MCHR2基因shRNA真核表达载体能有效抑制MCHR2基因的表达,减少B_max、升高K_d值及EC ₅₀,从而对MCHR2生物活性等特征产生影响.     

小菜蛾对阿维菌素的抗性遗传方式 和相对适合度研究

就小菜蛾Plutella xylostella对阿维菌素的抗性遗传方式和抗性品系的相对适合度进行了研究。室内选育的阿维菌素抗性品系与同源的敏感品系杂交、F₁代自交、F₁代与亲本回交,结果表明：杂交后的显性度（D）分别为-0.64和-0.52,说明小菜蛾对阿维菌素的抗性是常染色体、不完全隐性遗传;χ²检验证实,可能是多基因控制的抗性遗传。杂交F₁代乙酰胆碱酯酶（AChE）、羧酸酯酶（CarE）和谷胱甘肽转移酶（GST）活性比抗性亲本有所降低,F2代及回交后代三种酶的活性继续降低。种群适合度研究表明,抗性品系相对于敏感品系有0.84的适合度。     

桔小实蝇抗高效氯氰菊酯品系种群生命参数与相对适合度

系统观察了桔小实蝇抗高效氯氰菊酯品系和敏感品系试验种群在（28±2）℃下的生长发育和生殖情况,组建了两品系的实验种群生命表,分析了抗性种群与敏感种群的生态适合度差异.结果表明：抗高效氯氰菊酯品系(AlR₉₀)不同虫态的发育历期、平均世代历期、产卵前期均显著延长.与敏感品系相比,产卵高峰期抗性品系日产卵量不稳定,单雌产卵量、卵孵化率、成虫羽化率均显著下降,敏感品系平均每雌产卵量为324.0 粒、抗性品系仅为240.7粒.对实验种群生命表进行研究表明：抗高效氯氰菊酯品系的种群趋势指数(I=79.10)显著低于敏感品系(I=116.97);净生殖率R₀和内禀增长率r_m分别为1414.00和7.9463,均显著低于敏感品系(R₀=2184.00、r_m=8.3809).抗性品系的相对适合度仅为0.6474,研究结果表明桔小实蝇抗高效氯氰菊酯品系在繁殖和生长发育上存在明显的生存劣势.     

甜菜夜蛾对虫酰肼抗性的生化机制

为了解甜菜夜蛾Spodoptera exigua (Hübner)对虫酰肼的抗性生化机制, 采用活体测定法测定了甜菜夜蛾虫酰肼敏感种群、汰选种群和武汉自然种群体内解毒酶［羧酸酯酶（CarE）和谷胱甘肽-S-转移酶（GSTs)］、保护酶［过氧化氢酶(CAT)、 过氧化物酶（POD）和超氧化物歧化酶（SOD) ］以及与表皮形成相关的表皮酚氧化酶(PO)和几丁质酶的活性。结果表明: 汰选种群和自然种群CarE比活力分别是敏感种群的1.20和2.67倍, GSTs比活力分别是敏感种群的2.34和0.96倍。汰选种群CarE的Km值与敏感种群相比差异显著, 但V_max值无明显差异; 自然种群Km值和V_max值与敏感种群、汰选种群均存在极显著差异。酯酶同工酶电泳酶谱在迁移率、谱带数目、酶带染色深浅等方面均存在明显差异, 分析结果与CarE活力测定、酶动力学研究结果相符。与敏感种群相比, 汰选种群CAT和POD比活力差异不显著, SOD比活力显著增高; 自然种群3种酶比活力均显著增高; 自然种群和汰选种群均是SOD酶活力的变化较CAT和POD明显。汰选种群PO和几丁质酶比活力比敏感种群分别上升了37.64%和27.37%, 自然种群比活力分别上升了59.63%和60.29%。自然种群和汰选种群PO酶动力学常数均与敏感种群存在显著差异。     

云南不同菜区小菜蛾对三种生物农药的抗药性及其变化趋势

【目的】通过抗药性监测掌握滇中通海和滇西弥渡菜区小菜蛾Plutella xylostella(L.)种群对3种生物农药的抗药性水平及其变化趋势,为抗性治理提供技术支持。【方法】2008—2015年,在室内采用浸叶法测定了云南两个菜区小菜蛾种群对阿维菌素、多杀菌素和苏云金杆菌的抗药性。【结果】2008年抗药性测定结果表明,滇中通海、滇西弥渡菜区小菜蛾对阿维菌素和多杀菌素的抗药性水平均为高抗,对阿维菌素LC50值分别34.017和25.688 mg/L,抗性倍数为1 700.85和1 284.40倍;对多杀菌素LC50值分别13.728和19.830 mg/L,抗性倍数为114.40倍和165.25倍,两菜区对多杀菌素的抗性也为高抗;两菜区小菜蛾对苏云金杆菌敏感,LC50值分别0.530和0.538 mg/L,抗性倍数为2.04倍和2.07倍,属于抵抗水平。到2015年,通海和弥渡菜区小菜蛾种群对阿维菌素的抗性倍数分别下降到了455.70倍和255.05倍,下降趋势显著,但两菜区仍属高抗水平;对多杀菌素的抗药性下降趋势不显著,抗性倍数分别为35.56倍和75.28倍,为中抗水平,但年度间变化幅度较大,LC50为0.885~19.830 mg/L;两菜区对苏云金杆菌仍敏感,抗性倍数分别为5.41倍和1.73倍。【结论】总体上,2008—2015年度间有差异,通海和弥渡菜区小菜蛾种群对3种药剂的抗药性基本一致,对阿维菌素和多杀菌素的抗药性有所下降,但仍处于高抗水平,对苏云金杆菌一直保持在抵抗水平,建议生产上可以轮换使用苏云金杆菌,以提高对小菜蛾的持续控制效果。     

亚致死剂量阿维菌素和氟虫睛处理小菜蛾对寄生蜂菜蛾绒茧蜂生长发育的影响

分别在小菜蛾体内的菜蛾绒茧蜂处于卵期、早期幼虫和中期幼虫时,饲喂小菜蛾2龄幼虫亚致死剂量（＝LC₁₀）的阿维菌素和氟虫睛,研究上述杀虫剂处理对寄主体内菜蛾绒茧蜂结茧率和羽化率的影响。结果表明： 在菜蛾绒茧蜂处于卵期、早期幼虫和中期幼虫时,饲喂小菜蛾LC₁₀剂量阿维菌素处理的菜叶后,菜蛾绒茧蜂的结茧率分别下降26.6%,22.8%和5.8%,饲喂小菜蛾LC₁₀剂量氟虫睛处理的菜叶后,菜蛾绒茧蜂的结茧率分别下降76.9%,42.5%和18.5%。上述阿维菌素处理对菜蛾绒茧蜂成虫羽化率影响不显著,但上述氟虫睛处理可显著抑制菜蛾绒茧蜂成虫羽化率,在菜蛾绒茧蜂处于卵期、早期幼虫和中期幼虫时,饲喂小菜蛾LC₁₀ 剂量氟虫睛处理的菜叶可导致菜蛾绒茧蜂成虫羽化率分别下降53.1%,36.1%和47.8%。结果显示,即便是对寄主小菜蛾幼虫很低的剂量（LC₁₀剂量）也会显著危害小菜蛾幼虫体内的菜蛾绒茧蜂的生长发育。此外,饲喂小菜蛾幼虫亚致死剂量杀虫剂对菜蛾绒茧蜂生长发育的影响与杀虫剂种类及蛾绒茧蜂发育阶段有关。     

Effects of pentobarbital tolerance to and dependence on GABAB receptor binding

Effects of pentobarbital pellet implantation on [³H]baclofen binding in the frontal cortex of cerebellum of rat brains were examined. In the frontal cortex, pentobarbital tolerance caused an increase in the number of binding sites (B_max) without changing their affinity (K_D). Twenty-four hours after withdrawal of the pentobarbital pellets, there was a significant increase in the K_D and B_max values. Cerebellar binding, in contrast, was not significantly changed in any of the treatment groups. Addition of 1 mM of pentobarbital directly to binding assays using cortical membrane produced as increase in K_D without a change in B_max.In vitro, pentobarbital affected neither the K_D nor the B_max in the cerebellar [³H]baclofen binding. These results suggest that like the GABA_A receptor, [³H]baclofen binding to the GABA_B receptor in rat frontal cortex was affected by pentobarbital tolerance and dependence, and that there are regional differences in the properties of the GABA_B receptor.     

NICOTINE AND α-BUNGAROTOXIN BINDING TO AXONAL AND NON-NEURAL TISSUES1

Abstract— Nicotine binds to homogenates of lobster walking leg nerve (K_d= 1.1 ± 0.3 μm , B_max= 2.4 ± 0.5 nmol/g wet tissue), horseshoe crab leg nerve (K_d= 0.11 ± 0.06 μm , B_max= 1.3 ± 0.6nmol/g), and kidney from 18-month-old rats (K_d= 0.8 ± 0.2 μm , B_max= 23 ± 9 nmol/g). The pharmacological sensitivities of nicotine binding to lobster and horseshoe crab leg nerve homogenates are similar to that of the axonal cholinergic binding macromolecule (ACBM) (Denburg et al., 1972) of lobster leg. nerve membrane, while the binding to rat kidney is sensitive to α-bungarotoxin but not atropine or curare. There was no nicotine binding to rat heart or spleen, or to kidney from younger rats; little or no binding to blue crab nerve or to Torpedo electroplax motor nerve; and little binding (around 0.1 nmol/g) to rat liver. [³H]α-Bungarotoxin bound reversibly (0.17 nmol/g) to lobster leg nerve membrane The implications of these results for the distribution and function of the ACBM, and for the specificity of α-bungarotoxin, are discussed.     

Serotoninergic agonists and antagonists are the modulators of α1-Adrenoceptor activity in rat brain cortical membranes

The effects of activation and inhibition of serotonin receptors by serotonin (5-HT) and mianserin on the specific nonselective α₁-antagonist [³H]prazosine binding in rat cerebral cortex membranes was studied. It was shown that the ligand-receptor interaction of α₁-adrenoceptors corresponded to the model suggesting the presence of one pool of receptors and the binding of two ligand molecules to the receptor. The parameters of [³H]prazosine binding to α₁-adrenoceptors were as follows: K _d =1.85 ± 0.16 nM, B _max = 31.1 ± 0.3 fmol/mg protein, n = 2. In case of activation of 5HT-receptors by serotonin, the character of ligand binding was different: two pools of receptors were detected with the parameters K _d1 = 0.61 ± 0.04, K _d2 = 3.82 ± 0.15 nM, B _m1 = 6.6 ± 0.7, B _m2 = 25.6 ± 0.4 fmol/mg protein, n = 2. The sensitivity of the high-affinity pool increased threefold and the sensitivity of the low-affinity pool decreased twofold as compared to the control. The value of maximal reaction (B _max) did not change. In the case of inhibition of 5HT-receptors by mianserin, radioactive ligand is bound to α₁-adrenoceptors according to the same model as in the control conditions. The affinity of α₁-adrenoceptors to [³H]prazosine decreases twofold and the concentration increases (K _d = 3.97 ± 0.12 nM, B _max = 40.0 ± 0.5 fmol/mg protein). The data suggest that α₁-adrenoceptors in rat cerebral cortex exist as a dimer. The modulatory effects of serotonin and mianserin on the specific binding of [³H]prazosine to α₁-adrenoceptors was detected, manifesting itself as changes in the binding parameters and in the general character of ligand-receptor interactions.     

Glomerular thromboxane A2/prostaglandin H2 receptors: characterization and effect of adriamycin-induced nephrotic syndrome

We have characterized the thromboxane (TX) A₂/prostaglandin (PG) H₂ receptor in glomeruli isolated from the rat using the agonist radioligand [¹²⁵I]-BPO. Binding of [¹²⁵]-BOP was highly specific, stereoselective, and to a single class of high affinity binding sites (K_d = 1/16 ± 0.22 nM and B_max = 348 ± 32 fol/mg protein; n = 6). Binding of [¹²⁵I]-BOP was competed for by the agonist ONO11113 (K_d = 50.8 ± 8.0 nM; n = 4) and the antagonists SQ29548 (K_d = 15.8 ± 1.0 nM; n = 3), L657925 (K_d = 12.1 ± 2.2 nM; n = 3) and L65796 (K_d = 1642 ± 135 nM; n = 3). I-BOP also produced a TXA₂/PGH₂ receptor-mediated rise in [CA²⁺]_i in isolated glomeruli In adriamycin-induced nephrotic syndrome in the rat, the development of proteinuria is reported to be dependent on increased renal TXA₂ production. We therefore examined whether or not changes in glomerular TXA₂/PGH₂ receptors occur between control and nephrotic rats. No changes in expression of affinity of either glomerular or platelet TXA₂/PGH₂ receptors were observed. K_d and B_max values for isolated isolated glomeruli were 1.45 ± 0.24 nM and 406 ± 72 fmol/gm for controls and 1.22 ± 0.25 nM and 321 ± 62 fmol/gm for nephrotic rats (n = 6).     

β-Adrenoreceptor agonists and antagonists modulate the activity of α<Subscript>2</Subscript>-adrenoreceptors in rat cortex cerebral membranes

The influence of isoprenaline- and propranolole-induced activation and inhibition of β-adrenoreceptors on the specific nonselective α₂-antagonist [³H]RX821002 binding was studied on rat cerebral cortex subcellular membrane fractions. It was shown that the ligand-receptor interaction for α₂-adrenoreceptors corresponded to the model that assumed the presence of one receptor pool and binding of two ligand molecules to a receptor dimer. The following parameters were determined for [³H]RX821002 binding to α₂-adrenoreceptors: K _d1 = 1.57 ± 0.27 nM, B _max = 7.24 ± 1.63 fmol/mg of protein, n = 2. In the case of isoprenaline-induced activation of β-adrenoreceptors the binding of radiolabeled ligand to α₂-adrenoreceptors was described by the same model. The affinity of α₂-adrenoreceptors for [³H]RX821002 decreased more than twofold (K _d = 3.55 ± 0.02 nM) and the quantity of active receptors increased by 69% (B _max = 12.24 ± 0.06 fmol/mg of protein). Propranolole changed the model of ligand binding, and two pools of receptors were detected with the following parameters: K _d1 = 0.61 ± 0.02 nM, K _d2 = 3.41 ± 0.13 nM, B _ml = 1.88 ± 0.028 fmol/mg of protein, B _m2 = 9.27 ± 0.08 fmol/mg of protein, n = 2. The data suggest that α₂-adrenoreceptors in subcellular membrane fractions from rat cerebral cortex exist in dimeric form. Isoprenaline and propranolole exhibit modulating effect on the specific antagonist binding to α₂-adrenoreceptors, which results in the inhibition and alteration of [³H]RX821002 binding parameters.     

Endothelin-1 Binding to Endothelin Receptors in the Rat Anterior Pituitary Gland: Interaction in the Recognition of Endothelin-1 Between ETA and ETB Receptors

1. ¹²⁵I-Endothelin (ET)-1 binding to the rat anterior pituitary gland was saturable and single, with a K _d of 71 pM and a B _max of 120 fmol/mg.2. When 1.0 M BQ-123 (ET_A antagonist) was added to the incubation buffer, the binding parameters were 8.3 pM and 8.0 fmol/mg, whereas 10 nM sarafotoxin S6c (ET_Bagonist) exerted little change in these binding parameters (K _d,72pM;B _max, 110 fmol/mg).3. ET_B receptor-related compounds such as sarafotoxin S6c, ET-3, IRL1620, and BQ-788 competitively inhibited ¹²⁵I-ET-1 binding, only when 1.0 M BQ-123 was present in the incubation buffer.4. Thus, the ET_B receptor is capable of binding ET-1 when the ET_A receptor is being occupied by BQ-123. A collaboration mechanism between the ET_A and the ET_B receptor may function in the recognition of ET-1, a typical bivalent ligand.     

Pulmonary clearance of circulating endothelin-1 in dogs in vivo: exclusive role of ETB receptors

Dupuis, Jocelyn, Carl A. Goresky, and Alain Fournier.Pulmonary clearance of circulating endothelin-1 in dogs in vivo: exclusive role of ET_B receptors.J. Appl. Physiol. 81(4):1510-1515, 1996.The pulmonary circulation plays an importantrole in the removal of circulating endothelin-1 (ET-1). Plasma ET-1levels are increased in pulmonary hypertensive states of variousetiologies (e.g., idiopathic, heart failure, and congenital anomalies)in proportion to the severity of pulmonary hypertension. It is possible that reduced pulmonary clearance of this peptide contributes to thehyperendothelinemia of those pathologies. TheET_A andET_B receptors are abundant in lungtissues: on the vascular endothelium, theET_B receptor is predominant andmay contribute to ET-1 extraction through receptor-mediatedendocytosis. We designed experiments to determine and quantify theimportance of the ET_A andET_B receptors in the pulmonaryextraction of circulating ET-1 in anesthetized dogs. The single-passcumulative tracer ET-1 extraction by the lung was measured with theindicator-dilution technique before and 5 min after intrapulmonaryinjection of the specific ET_Aantagonist BQ-123 (n = 5, 120-960nmol) and the specific ET_Bantagonist BQ-788 (n = 6, 1,000 nmol).The inhibitors had no significant effect on pulmonary and systemichemodynamics. Mean cumulative pulmonary ET-1 extraction was notmodified by BQ-123 [control (C): 36 ± 4%, antagonist (A): 34 ± 6%] but was completely abolished by BQ-788 (C: 34 ± 6%, A: 0 ± 2%, P < 0.001). Thepulmonary rate constant (K) for ET-1removal was also unaffected by BQ-123 (C: 0.050 ± 0.0085 s¹, A: 0.047 ± 0.012 s¹) but significantlydecreased and became close to zero after BQ-788 (C: 0.058 ± 0.014 s¹, A: 0.009 ± 0.007 s¹,P < 0.001). We conclude that theET_B receptor is completely andexclusively responsible for pulmonary ET-1 removal in vivo. Futurestudies are needed to show whether desensitization or downregulation ofthe ET_B receptor may contribute tothe increase in circulating ET-1 levels in conditions associated withpulmonary hypertension. This novel pulmonary endothelial cell functionmay play a protective role by modulating circulating ET-1 levels in thesystemic circulation.

     

Allosteric effects of atropine and carbachol on the activity of α<Subscript>2</Subscript>-adrenoceptors in rat brain cortex membranes

Activation and inhibition of muscarinic cholinoceptors by atropine and carbachol are shown to exert allosteric effects on the binding of specific nonselective α₂-adrenoceptor antagonist [³H]RX821002 in rat brain cortex membranes. The ligand-receptor interaction for α₂-adrenoceptors corresponded to the model suggesting the presence of one homogeneous pool of receptors with two specific binding sites. The parameters of the [³H]RX821002 binding were as follows: [³H]RX821002 -K _d = 1.94 ± 0.08 nM, B _max = 13.4 ± 1.8 fmol/mg protein, n = 2. The inhibition of muscarinic cholinoceptors by atropine induced an increase of affinity (K _d = 1.36 ± 0.12 nM) and a decrease of the α2-adrenoceptor density (B _max = 10.18 ± 0.48 fmol/mg protein). The muscarinic cholinoceptor agonist carbachol induced an increase of the affinity (K _d = 1.56 ± 0.05 nM) and quantity of binding sites (B _max = 16.61 ± 0.29 fmol/mg protein). As a result, under the influence of atropine and carbachol, the efficiency of binding (E = B _max/2K _d) increased from 3.50 ± 0.40 to 5.60 ± 0.79 and 6.86 ± 0.20 fmol/mg protein/nM, respectively. The data suggest that α₂-adrenoceptors exist in rat brain cortex as homodimers.     

不同地理种群两针松光合和生长特性的差异

为认识两针松中的赤松（Pinus densiflora）、长白松（Pinus sylvestris var. sylvestriformis）和樟子松（Pinus sylvestris var. mongolica）光合作用对环境变化的响应和适应特征,在其自然分布区内选择地理和气候差异显著的9个地理种群,采集成熟种子并播种于东北林业大学温室,2 a后,测定针叶的光合能力及其相关因子,并同时测定幼苗的株高和基径,比较种间和地理种群间差异。结果表明：赤松、长白松和樟子松种间最大光合速率（p=0.34）、呼吸速率（p=0.15）和表观量子效率（p=0.18）的差异均不显著;地理种群间表观量子效率（AQY）差异显著(p=0.08),其中兴凯湖种群表观量子效率最高,为0.084 5±0.002 4 mol CO₂·mol^-1 photons,较其他种群高13.10%~159.23%。地理种群间呼吸速率(R_d)差异显著(p=0.01),黑河和兴凯湖种群的呼吸速率最高（分别为1.62±0.18 μmol CO₂·m^-2·s^-1,1.52±0.30 μmol CO₂·m^-2·s^-1）,安图和东宁种群的呼吸速率最低,分别为0.40±0.01 μmol CO₂·m^-2·s^-1,0.34±0.03 μmol CO₂·m^-2·s^-1。地理种群间最大净光合速率(P_max)差异显著(p=0.02),其中兴凯湖、东宁、韩国、鸡东、二道白河、红花尔基种群的最大光合速率差异不显著,均值为18.36±1.81 μmol CO₂·m^-2·s^-1,高于安图、漠河、黑河种群。安图、漠河、黑河种群间最大光合速率差异不显著,均值为12.57±0.86 μmol CO₂·m^-2·s^-1。地理种群间的株高和基径差异均显著,其中韩国种群株高最高,黑河种群最低;基径兴凯湖种群最高,安图种群最低。株高和基径最大值约为最小值的3倍。两针松针叶的光合能力及其一些相关因子的地理种群间差异可能是其光合机构对种源地环境条件长期生理适应的结果。