【摘要】 目的：观察密蒙花提取物滴眼剂对去势所致干眼症雄鼠基础泪液分泌量、泪膜稳定性、泪腺中雄激素受体表达的影响，探讨密蒙花提取物滴眼剂抗雄激素水平下降所致干眼症的作用机制。
方法：将45只Wister雄性大鼠随机分为空白组(A1、A2、A3)、模型组(B1、B2、B3)、密蒙花提取物滴眼剂治疗组(C1、C2、C3)，共9组，1代表饲养1mo，2代表饲养2mo，3代表饲养3mo，每组5只，对B、C组行去势术建立动物模型，对C组以密蒙花提取物滴眼剂连续滴眼治疗1mo，对全部实验大鼠行Schirmer I试验、测量泪膜破裂时间，采用流式细胞仪检测泪腺中雄激素受体的表达。结果：C组Schirmer I试验测量值明显高于B组(P<0.01)，泪膜破裂时间明显长于B组(P<0.01)，显示密蒙花提取物滴眼剂能够显著维持泪腺基础分泌量和泪膜的稳定性;C组流式细胞仪检测的AR阳性表达率明显高于B组，显示密蒙花提取物滴眼剂中的有效成分可能有拟雄激素的效应。论：密蒙花提取物滴眼剂中主要成分为黄酮类物质，可显著抑制雄激素水平降低后大鼠干眼症的发生，其作用机制可能与黄酮类物质结构与雄激素类似，可以起到拟雄激素效应，从而维持泪腺基础分泌量和泪膜的稳定性。
【关键词】 去势;干眼症;泪腺;雄激素受体;拟雄激素效应;密蒙花提取物;滴眼剂
14 Wu SZ, Lv HS, Wu YX. Effect of androgen on expression of AR and ER gene of smooth muscle of old rabbits. Zhonghua Laonian Yixue Zazhi 2002;1(2):114116AbstractAIM: To evaluate the effects of the extract of Buddleja officinalis eye drops in basic tears secretory volume， tear film stability, expression of androgen receptors(AR) in castrated rats with dry eye， and to investigate the therapeutic effects of extract of Buddleja officinalis on dry eye caused by gonadal hormones level imbalance. METHODS：A total of 45 Wistar masculinity rats were divided at random into 9 groups， including normal group(A1，A2 and A3)， model group(B1，B2 and B3)， therapy group with extract of Buddleja officinalis eye drops(C1，C2 and C3). The “1” stood for being fed for 1 month, and “2” for 2 months, and “3” for 3 months. The dry eye model was established with orchiectomy on group B，C. Group C was treated with Buddleja officinalis extract eye drops for one month. All rats were checked with Schirmer Ⅰ test (SⅠt) and tear film breakup time (BUT). Expression of AR was analyzed by flow cytometer(FCM). RESULTS：The SⅠt value of group C was significantly higher than that of group B (P<0.01) and the BUT value of group C was significantly longer than that of group B (P<0.01), which indicated the eye drop could significantly keep basic tears secretory volume and tear film stability. And the expression of AR of group C was much higher than that of group B，which showed that available composition of the eye drops maybe display androgenlike activity.CONCLUSION：The main components of extract of Buddleja officinalis is the flavonoids which could significantly inhibit happening of dry eye of rat after androgen level lowered. Its mechanism is like androgen's and it could display androgenlike activity to keep basic tears secretory volume and tear film stability.
KEYWORDS：castrate; dry eye; lacrimal gland; androgen receptors; androgenlike activity; extract of Buddleja officinalis; eye drops
Peng QH, Yao XL, Wu QL, Tan HY, Zhang JR.
Effects of extract of Buddleja officinalis eye drops on androgen receptors of lacrimal gland cells of castrated rats with dry eye. Int J Ophthalmol(Guoji
Yanke Zazhi) 2010;10(2):203208
INTRODUCTION
Dry eye could affect people’s work and life by significant declining in sight. Although it may not threaten people’s lives , it possesses a high incidence and has been a top issue in recent research. Androgen level declining is the main cause of dry eye. In present therapies, substitute therapy of androgen is the only therapy that could treat dry eye caused by gonadal hormones imbalance, but long use of this therapy will inevitably bring many side effects. There are some other therapies which also have certain flaws and limitations. Buddleja officinalis is a drug stored by Chinese medicine, and its often used to treat eyes with flavonoids as its effective parts. Androgen and flavonoids compounds are all heterocyclic polyphenols compounds, so the similarity in their chemical structures can be used to expound their endogenous androgen effect to treat some eye disease caused by gonadal hormones level imbalance including dry eye caused by imbalance of gonadal hormones level. The extract of Buddleja officinalis eye drops are made to follow the characteristic of partial treatment for surface diseases of eyes, make model from dry eye of rat for research, and aim to investigate the effect mechanism and the therapeutic effects of Buddleja officinalis on dry eye caused by imbalance of gonadal hormones level.
MATERIALS AND METHODS
Materials A total of 45 onemonthold healthy Wistar male rats weighing approximately 200g were purchased from animal experimental center of Hunan University of Traditional Chinese Medicine. Animals with following features were used: the front and ground eyes were normal after being checked by slit lamp microscope and retinoscope, the SⅠt value was no less than 10mm/5min and the BUT value 10s after the surface anaesthesia with 5g/L cocain eyedrops. Extract of Buddleja officinalis eye drops were made by the Department of Pharmacy of the First Affiliated Hospital of Hunan University of Traditional Chinese Medicine. The comparison products of linarin (Medical Biology Products Checking Bureau, China, containing 98.3%).
Cytoperm(5g/L saponin solution, BD company). Rat antihuman AR and FITCIgG(Wuhan Boshide Biology and Engineer Ltd Co). Liquid 15252996 high performance liquid chromatography(USA Water Company, containing 2996 test machine of two polar tubes, 1525 and 717 automatic sample machine); Empower Chinese Chromatographic Work Station(USA Water Company); Photometer of ultraviolet visible light of double beams (Beijing Limited Liability Corporation of Puxin General Equipment); Flow cytometer(FACS type, USA BD company).
Buddleja officinalis dry buds were extracted two times in alcohol for centrifugal filtration, the filtrate was on HPD100 macroporous resin column, and eluted with ethanol. 70% ethanol eluation fluid were collected, dried and smashed to be extract of Buddleja officinalis. Columns: Phenomenex×Gemini Cl8, Mobile phase: Methanol0.1% phosphoric acid 55∶45，v/v); Velocity: 0.8mL/min; Detection wavelength: 326nm; Column temperature: 30℃; Injection volume: 10μL. Linarin standard solution was prepared as a control, using external standard method to calculate. Linarin content was prepared as a control to establish the standard curve of UV and total flavonoids of Buddleja was measured in UV determination.
Extract of Buddleja officinalis dissolved in distilled water extract, quality ratio of water vs extracts was 1∶0.1 ,adding eye lubricant carboxymethyl cellulose, the concentration of control of 1.5%, by adding potassium bicarbonate and potassium chloride as buffer system, the concentration of control at 0.1% or less. At this time physical and chemical properties testing pH, osmotic pressure, specific gravity and refractive index were adjusted to achieve the following criteria: ①pH value:7.37.8; ②osmotic :311350mOsm; ③weight: approximately equal to 1; ④refractive index: 1.336. Finally adding preservatives benzalkonium bromide, the concentration was 0.005%.
Methods The 45 big male rats were randomly divided into 9 groups , i.e. A1, B1, C1, A2, B2, C2, A3, B3, C3, five for each group. The A stood for fake operation normal group(short for normal group as follows), the B stood for operation control group(short for control group), and the C stood for therapy group with Buddleja officinalis extract eye drops(short for therapy group); the “1” stood for being fed for 1 month, the “2” stood for being fed for 2 months and the “3” stood for being fed for 3 months. Ma [1]method was referred to make animal model: the orchiectomy of double sides: experimental rats from B1, B2, B3, C1, C2, C3 groups were fed by either food or water 12 hours before the experiment, their outside muscle of back thigh were disinfected by iodide, and they were anesthetized with 30mg/kg infection of ketamine hydrochloride through abdomen. As to male rats , they were on their backs with four limbs open and fixed, the hair in their lower abdomen were faded by special medicament, and their hypescrotum were partially anesthetized with 20g/L ridocaine, and were disinfected by iodide. Then they were put on a germfree sheet, and one testicle was squeezed into scrotum through peritoneum to be prevented from slipping. After that, the scrotum was cut a hole with a disinfecting knife, and the testicle was squeezed out with force, then the vein and tube of sperm duct were tightly pricked and the testicle and attaching testicle were cut off. After the scrotum skin partial iodine was sewed and disinfected in case of infection. The other testicle and the attaching testicle were cut in the same way. As to the animals in A1, A2, A3 groups, only scrotum was cut, and the scrotum skin was constantly sewed after the operation. 200000 U penicillin was injected into the muscle before the operation, and 200000 U penicillin was injected with continuous three days muscle infection after the operation in case of infection. Group A1 and B1 were dropped with saline eye drops everyday, three drops per day and group C1 was dropped with Buddleja officinalis eye drops everyday, one drop per day. All of the three lasted one month, and after one months normal feeding, animals in these three groups were killed. Group A2 and B2 were dropped with saline eye drops everyday, three drops per day and group C2 was dropped with Buddleja officinalis eye drops everyday, one drop per day. All of the three lasted two months, and after two months normal feeding, animals in these three groups were killed. Group A3 and B3 were dropped with saline eye drops everyday, three drops per day and group C3 was dropped with Buddleja officinalis eye drops everyday, one drop per day. All of the three lasted three months, and after three months normal feeding, animals in these three groups were killed.
The 45 male rats were respectively made SⅠt and BUT tests. The first time was before the rats were divided, and the other was after the last prescription was taken by the rats. The standard of the tests referred to the diagnoses standard of SⅠt and BUT. Animals heads were cut down as soon as the SⅠt and BUT tests were finished, and lacrimal gland were removed at once, then fixed with over 40g/L formaldehyde for the checking of flow cytometer.
The lacrimal gland tissues were washed with the normal saline, cut into pieces, washed again with saline. The cell suspension were collected, then centrifugally washed for 2 times with normal saline, centrifugally washed again and the supernatant were abandoned. The tubes were added cytoperm with 500μL PBS5g/L paraformaldehyde to break film. The supernatant was absorbed after centrifugation. Then added mouse antihuman 1∶40 AR(I resistance), and control tubes were added man equivalent IgG1Kappa I resistance with the same type. After the mixture was shook to make homogeneous, put in a warm room for 30 minutes in shadow. Then it was centrifuged, the supernatant was abandoned, washed with PBS for 2 times. Two tubes were added respectively into 1∶80 FITCIgG100μL(II resistance), and after the mixture was shook to make homogeneous, put in a warm room, 30 minutes in shadow, and then it was centrifuged, the supernatant was abandoned, washed with PBS for 2 times. Again centrifugation, the supernatant was abandoned and the cells were suspended in 500μL PBS5g/L paraformaldehyde for test.
The flow cytometry of FACS type made in American BD company was applied to measure. Before the test the chicken erythrocytes were taken as standard sample to adjust the apparatus coefficient of variation. 1000000 cells of each sample were tested. The quantitative analysis for androgen receptor flow cytometer uses depent on the intensity of specific fluorescence. And this number varied with the combined digit capacity of the androgen receptor on each cell. Analyze relative fluorescence intensity(RFI), (RFI equals the average fluorescence intensity in the test tube mining the average fluorescence intensity in the control tube), and the result was shown with positive expression rate.
Statistical Analysis Data were analyzed the patches statistically with SPSS 13.0 software, and tested both sides. P≤0.05 means difference has statistical significance.
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