2. Material and Methods
2.1. Animal Location
In this study, an equal number of male and female giant pandas aged between 2 and 28 years were included. They showed no abnormalities in their eating, drinking, or excretion two weeks before blood collection. The pandas were housed at the Beijing Zoo, with geographical coordinates at 39.9° N, 116.3° E. The basic information about giant pandas can be found in
Table 1 and
Table 2. The bamboo species primarily provided to giant pandas at the Beijing Zoo include
Phyllostachys propinqua (mao bamboo) and
Pleioblastus amarus (qing bamboo), supplemented with bamboo shoots and mantou (steamed buns). There were no significant variations in the energy, carbohydrate, and protein intake of giant pandas across the four seasons.
2.2. Season and Climate
The study was conducted continuously for two years, starting from mid-2018 and ending at the end of June 2020. Based on the regular climate patterns in Beijing, each year was divided into seasons as follows: spring includes February, March, and April; summer includes May, June, July, and August; autumn encompasses September and October; and winter spans from November to January. Beijing, China experiences a temperate monsoon climate characterized by hot and rainy summers and cold, dry winters. During the experimental period, the average temperature in spring ranged from 1 to 18 °C with an average relative humidity of 29%. Summer had an average temperature between 19 °C and 30 °C with an average relative humidity of 45%. Autumn had an average temperature range of 17 to 29 °C with an average relative humidity of 52%, and winter had an average temperature range of −3 to 6 °C with an average relative humidity of 37%.
2.3. Blood Sampling
Twelve giant pandas underwent monthly blood collection procedures under operant conditioning. All participating pandas had successfully completed positive reinforcement training. On the day of sampling, the pandas were fasted from midnight until 8 a.m. The blood samples were collected from the median vein in the front limb of the giant pandas, with each sample totaling 5 mL. These samples were placed in EDTA (Yuli, Jiangsu Yuli Medical Equipment Co., Ltd., Taizhou City, China) anticoagulant tubes for storage and were subjected to blood analytes within a two-hour timeframe.
2.4. Sample Treatment
The blood cell counts were determined using manual microscopy by trained laboratory personnel on a blood cell counting board. Hemoglobin levels were measured using the cyanide-free high-iron hemoglobin method. Red blood cell hematocrit values were determined using the Winslow method. Blood biochemical parameters were measured using the FUJI DRI-CHEM NX500iVC, a fully automatic dry chemistry analyzer made by FUJIFILM, Tokyo, Japan.
Hemorheology parameters were assessed using the HT-100A blood rheological viscosity tester produced by Zibo Hengtuo Analysis Instruments Co., Ltd., Zibo City, China. Whole blood viscosity was measured at shear rates of 3 S-, 30 S-, and 200 S-. Plasma viscosity was determined after centrifugal separation of anticoagulated blood.
2.5. Environmental Temperature and Body Temperature
Data from September 2018 to August 2020 were compared. Independent sample t-tests were conducted based on the monthly average temperature provided by the observatory. Due to multiple comparisons, the Bonferroni adjustment was applied to the significance level. Each giant panda’s body temperature was measured using an infrared ear thermometer inserted directly into the ear.
2.6. Statistical Analysis
The collected data were analyzed using GraphPad Prism software (
https://www.graphpad.com/features) for statistical analysis. The article employed repeated measures analysis of variance (ANOVA) for statistical comparisons and conducted multiple comparisons using Fisher’s protected least significant difference (LSD) test. A
p-value less than 0.05 was considered statistically significant.
According to the Shapiro–Wilk test, the data from each group were found to follow a normal distribution. However, the sphericity assumption test results indicated that the assumption of sphericity was not met. Therefore, the corrected results from the Greenhouse–Geisser test were used in the one-way analysis of variance.
2.7. Ethical Standards
This study was conducted on giant pandas, which are national treasures, and informed consent was obtained from the Beijing Zoo to collect data. During the research period, all animals underwent positive reinforcement training in accordance with official guidelines and regulations. These guidelines represent technical standards for the production, care, and use of (wildlife) animals.
4. Discussion
This study, by examining the age and seasonal variations in blood parameters of captive giant pandas in northern China, provides a baseline for future blood analyte comparisons in non-anesthetized captive giant pandas and offers valuable insights for the medical care of giant pandas in zoos. Based on the parameters collected in this study, if factors such as age and season are not considered, there are significant differences compared to the reference range of the pandas in Beijing Zoo. The main differences are reflected in the following: an increase in hemoglobin, red blood cell count, white blood cell count, and hematocrit; a decrease in blood glucose, total protein, albumin, globulin, triglycerides, uric acid, creatinine, total bile acid, alanine aminotransferase, aspartate aminotransferase, creatine kinase, cholinesterase, gamma-glutamyl transpeptidase, and amylase; and an increase in urea nitrogen, total cholesterol, lactate dehydrogenase, alkaline phosphatase, adenosine dehydrogenase, and alpha-hydroxy acid dehydrogenase. Analyzing the reasons for these changes, although the existing reference range in Beijing Zoo includes a total of 29 pandas, it also includes samples collected after anesthesia, and the influence of stress on blood analytes cannot be ruled out. Therefore, the reference range cannot be regarded as the average level of the tested animals. The blood samples measured in this study were all collected from non-anesthetized captive giant pandas. We hope that these data can contribute to enriching and enhancing the reference range for giant pandas at Beijing Zoo, providing valuable references for the blood parameters of pandas in the zoo in the future.
Specific lifestyles can lead to welfare issues in various wild animals kept in captivity, including poor health, repetitive stereotypical behavior, and breeding difficulties [
9]. Analyzing hematological and biochemical parameters is an important part of assessing the physiological, nutritional, and pathological conditions of animals. Determining the levels of biochemical blood parameters is important for evaluating the physiological status of animal organisms as it enables the diagnosis of various diseases affecting internal organs. The reports by Deng and Luo et al. indicate that age significantly affects various hematological and biochemical indicators [
10,
11]. In this study, age influenced hematological parameters, hemorheology, serum enzymes, serum proteins, and serum metabolites. It was found that the elderly group of giant pandas had the lowest levels of glucose, hematocrit, hemoglobin, WBC, and urea as well as the highest levels of globulin, AST, CRE, and BUN, which may be related to the aging state of the giant pandas in Beijing Zoo or perhaps chronic stress. However, based on the analysis of ALT, CK, creatinine, and urea, all animal groups in the experiment showed normal values for these parameters; therefore, although the values of the elderly group of pandas showed significant changes, the animals were not in a diseased state. The alkaline phosphatase level in the sub-adult group was significantly higher than in the adult and elderly groups, which may be due to the fact that alkaline phosphatase can reflect bone formation and osteoblast metabolic activity, thus leading to higher levels in young animals. In clinical practice, we currently only know that the differences need to be treated accordingly, which can help clinical practitioners make correct and objective assessments when managing health [
12].
This study found seasonal variations in hematological parameters, hemorheology, and serum enzymes. The seasonal changes in serum enzymes may be related to the spring estrus of giant pandas. Meanwhile, hematological parameters, such as HGB and RBC, were higher in winter. The plasma viscosity (
p < 0.05), erythrocyte aggregation index (
p < 0.05), and erythrocyte rigidity index (
p < 0.05) showed significant seasonal variations. These findings may indicate a regulatory role of seasonal changes in blood viscosity in giant pandas. Clinical studies have found that many diseases are accompanied by abnormalities in various hemorheological indicators. Some of these abnormal indicators often appear earlier than symptoms or signs, and they often lag behind when symptoms or signs disappear during recovery [
13,
14,
15]. Blood viscosity is mainly determined by red blood cell hematocrit, plasma viscosity, red blood cell aggregation, and red blood cell deformability [
14,
16]. Similarly, it has been shown that the effective viscosity of circulating blood increases as plasma osmotic pressure increases with age [
17]. There is a significant difference in the red blood cell aggregation index between summer and winter. Therefore, the main reason for increased whole blood viscosity may be due to red blood cell aggregation. Studies have shown that ambient temperature (climate) has an effect on both blood viscosity and plasma viscosity in animals [
18,
19,
20,
21]. When the temperature decreases, blood flow slows down, blood viscosity increases, and red blood cell aggregation is enhanced [
22,
23,
24]. This is because, during cold weather, animals need to consume a large amount of oxygen to generate heat to maintain a relatively stable body temperature. Inhaling cold air can also increase pulmonary artery pressure, leading to impaired gas exchange and tissue hypoxia, resulting in increased quantities of red blood cells [
25,
26,
27]. This may explain the observed seasonal variations in blood parameters in pandas in this study. Additionally, the activity rhythm of many animals is significantly influenced by seasonal changes, and activity levels are directly related to temperature. When activity levels increase, the surface area of red blood cells relatively increases, which facilitates the release of oxygen from red blood cells and the removal of carbon dioxide from tissues, accelerating the gas exchange rate. This also reduces blood viscosity and increases blood flow velocity. However, there is currently a lack of seasonal research on the behavioral patterns or activity levels of giant pandas, and further related research is needed.
A successful ex situ conservation project has required us not only to save an animal species but also research the appropriate thermal environment for individual animal survival in order to develop corresponding conservation strategies [
28]. The construction of a comfortable and reasonable animal house is one of the important conditions for the captive survival and health of giant pandas, and the control of the indoor environmental quality is directly related to the health of the giant pandas. Some scholars have paid attention to the need to set up regulating measures to reduce heat stress in giant pandas during high temperatures in summer [
29]. However, this study shows that even though giant pandas are believed to tolerate cold environments, hemorheology is often a forgotten factor in vascular health. The risks of changes in hemorheology in giant pandas during the winter (cold) period and their clinical relevance to vascular diseases should still be considered when housing and feeding them. Future research directions may include the following aspects: exploring the impact of different ages and seasons on the metabolic activity of captive giant pandas and further studying the activity changes and differences in the overall metabolic processes of giant pandas in different age groups to understand their physiological and metabolic needs at different stages and find suitable feeding and management methods for giant pandas of different age groups. At the same time, continuing to explore the effects of factors such as seasons and climate on giant pandas, and whether these factors may lead to environmental stress, thus affecting the health and survival status of giant pandas, is warranted. In-depth study of the relationship between blood viscosity and the health condition of giant pandas would be beneficial, necessitating analysis of the negative effects of blood viscosity on giant pandas and exploring the relationship between blood viscosity and the health condition of giant pandas. Monitoring and analyzing the changes in blood viscosity of giant pandas over a long period of time can help to identify the risk of giant pandas getting sick early and take corresponding treatment and preventive measures. Studying the effects of environmental factors on the physiology and behavior of giant pandas to understand further the effects of environmental factors such as temperature, humidity, and lighting on the physiology and behavior of giant pandas is another area that could be further explored. By controlling and improving the environment of giant pandas, a more suitable captive environment can be provided.